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NZ618727B2 - Compounds having muscarinic receptor antagonist and beta2 adrenergic receptor agonist activity - Google Patents

Compounds having muscarinic receptor antagonist and beta2 adrenergic receptor agonist activity Download PDF

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Publication number
NZ618727B2
NZ618727B2 NZ618727A NZ61872712A NZ618727B2 NZ 618727 B2 NZ618727 B2 NZ 618727B2 NZ 618727 A NZ618727 A NZ 618727A NZ 61872712 A NZ61872712 A NZ 61872712A NZ 618727 B2 NZ618727 B2 NZ 618727B2
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New Zealand
Prior art keywords
phenyl
methyl
amino
hydroxy
ethyl
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NZ618727A
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NZ618727A (en
Inventor
Gabriele Amari
Matteo Biagetti
Ian Linney
Fabio Rancati
Andrea Rizzi
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Chiesi Farmaceutici Spa
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Priority claimed from PCT/EP2012/060795 external-priority patent/WO2012168359A1/en
Publication of NZ618727A publication Critical patent/NZ618727A/en
Publication of NZ618727B2 publication Critical patent/NZ618727B2/en

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    • A—HUMAN NECESSITIES
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425—Thiazoles
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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/439—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom the ring forming part of a bridged ring system, e.g. quinuclidine
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    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4525—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
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    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4704—2-Quinolinones, e.g. carbostyril
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    • A61K31/47—Quinolines; Isoquinolines
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    • A61K9/0073—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
    • A61K9/0078—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy for inhalation via a nebulizer such as a jet nebulizer, ultrasonic nebulizer, e.g. in the form of aqueous drug solutions or dispersions
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    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
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    • C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
    • C07C215/46—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • C07C215/48—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by hydroxy groups
    • C07C215/50—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by hydroxy groups with amino groups and the six-membered aromatic ring, or the condensed ring system containing that ring, bound to the same carbon atom of the carbon chain
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    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/40—Oxygen atoms
    • C07D211/44—Oxygen atoms attached in position 4
    • C07D211/46—Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4
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    • C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
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    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
    • C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
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    • C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems

Abstract

Provided are compounds of the general formula (I), wherein the variables are as defined in the specification. Examples of the compounds include (R)-Quinuclidin-3-yl (3-(9-((R)-2-hydroxy-2-(8-hydroxy-2-oxo-1,2-dihydroquinolin-5-yl)ethylamino)nonyloxy)phenyl)(phenyl)-methylcarbamate and (2S)-4-(((R)-2-hydroxy-2-(8-hydroxy-2-oxo-1,2-dihydroquinolin-5-yl)ethyl)amino)butyl 3-phenyl-2-(4-((3-(phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)methyl)phenoxy)methyl) benzamido)propanoate. The compounds have muscarinic receptor antagonist and beta2 adrenergic receptor agonist activity. The compounds may be useful in the treatment of respiratory disorders such as asthma, chronic bronchitis or chronic obstructive pulmonary disease (COPD). -hydroxy-2-(8-hydroxy-2-oxo-1,2-dihydroquinolin-5-yl)ethyl)amino)butyl 3-phenyl-2-(4-((3-(phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)methyl)phenoxy)methyl) benzamido)propanoate. The compounds have muscarinic receptor antagonist and beta2 adrenergic receptor agonist activity. The compounds may be useful in the treatment of respiratory disorders such as asthma, chronic bronchitis or chronic obstructive pulmonary disease (COPD).

Description

COMPOUNDS HAVING MUSCARINIC RECEPTOR ANTAGONIST AND BETA2 ADRENERGIC RECEPTOR AGONIST ACTIVITY FIELD OF THE INVENTION The present invention relates to compounds of general formula I, acting both as muscarinic receptor antagonists and beta2 adrenergic receptor agonists, to processes for their preparation, to compositions comprising them, to therapeutic uses and combinations with other pharmaceutical active ingredients.
BACKGROUND OF THE INVENTION Pulmonary disorders, such as asthma and chronic obstructive pulmonary disease (COPD), are commonly treated with bronchodilators. A well known class of bronchodilators consists of beta-2 adrenergic receptor agonists, such as salbutamol, fenoterol, formoterol and salmeterol. These compounds are generally administered by inhalation.
Another well known class of bronchodilators consists of muscarinic receptor antagonists (anticholinergic compounds), such as ipratropium and tiotropium. These compounds are also typically administered by inhalation.
Inhaled formulations of both beta-2 agonists and muscarinic receptor antagonists are valuable agents in the treatment of asthma and COPD, with both classes of agents providing symptomatic relief due to their ability to relax constricted airways. Observations that the bronchodilator effects of the two classes of agents were additive, prompted studies with combinations of the two agents. In 1975, it was shown that that beneficial effects could be achieved by combining two ingredients such as fenoterol and ipratropium bromide in a single aerosol. This prompted the development of fixed dose combinations of ipratropium bromide firstly with fenoterol (Berodual, 2 introduced in 1980), and then with salbutamol (Combivent, introduced in 1994).
More recently the availability of both long-acting muscarinic antagonists and long-acting beta-2 agonists prompted to the development of combinations of these agents. For example, WO 00/69468 discloses medicament compositions containing a muscarinic receptor antagonist, such as tiotropium bromide, and beta-2 adrenergic receptor agonists, such as formoterol fumarate or salmeterol, and WO 2005/115467 discloses a combination which comprises a beta-2 agonist and an antagonist of M3 muscarinic receptors which is a salt of 3(R)-(2-hydroxy-2,2-dithien ylacetoxy)(3-phenoxypropyl)azoniabicyclo[2.2.2]octane.
An alternative approach to the development of fixed dose combinations is the identification of molecules that combine both activities of muscarinic antagonism and beta-2 agonism. In fact compounds possessing both beta-2 adrenergic receptor agonist and muscarinic receptor antagonist activity are highly desirable since such bifunctional compounds would provide bronchodilation through two independent mechanisms of action while having a single molecule pharmacokinetics.
Such kind of compounds was described in some patent applications, such as WO 2004/074246, WO 2004/074812, WO 2005/051946, WO 2006/023457, WO 2006/023460, WO 2010/123766 and WO 2011/048409.
It has now been found that some particular carbamate derivatives, besides possessing both beta-2 adrenergic receptor agonist and muscarinic receptor antagonist activity, possess elevated affinity for the M3 muscarinic receptors and long lasting bronchodilating activity.
SUMMARY OF THE INVENTION The present invention relates to compounds of general formula I, acting both as muscarinic receptor antagonists and beta2 adrenergic receptor 3 agonists, to processes for their preparation, to compositions comprising them, to therapeutic uses and combinations with other pharmaceutical active ingredients among which are, for instance, those currently used in the treatment of respiratory disorders, e.g. corticosteroids, P38 MAP kinase inhibitors, IKK2, HNE inhibitors, PDE4 inhibitors, leukotriene modulators, NSAIDs and mucus regulators.
DETAILED DESCRIPTION OF THE INVENTION In particular, the invention is directed to compounds of general formula I wherein Q is a group of formula Q1, Q2, Q3, Q4, Q5 or Q6 Z is H or OH; Y is selected from Y’ and Y1 which are divalent groups of formula Y’ 4 or Y1 wherein A1 and A2 are independently absent or are selected from the group consisting of (C1-C12)alkylene, (C3-C8)cycloalkylene and (C3-C8)heterocycloalkylene optionally substituted by one or more substituents selected from the group consisting of (C1-C6)alkyl, aryl(C1-C6)alkyl and heteroaryl(C1-C6)alkyl; B is absent or is selected from the group consisting of (C3-C8)cycloalkylene, (C3-C8)heterocycloalkylene, arylene, heteroarylene or is a group of formula B1 optionally substituted by one or more groups selected from halogens, nitrile, (C1-C6)alkyl, (C1-C6)alkoxy and aryl(C1-C6)alkyl; C is absent or is selected from the group consisting of -O-, -CO-, -OC(O)-, -C(OO)-, -S-, -S(O)-, -S(O)2- and -N(R7)-, or is one of the following groups C1-C18 wherein R7 is H or is selected from the group consisting of linear or branched (C1-C8)alkyl, (C3-C8)cycloalkyl, (C3-C8)heterocycloalkyl, aryl, aryl(C1- C6)alkyl, (C1-C6)alkoxy(C1-C6)alkyl and heteroaryl and R8 is (C1-C8)alkoxycarbonyl; D is absent or is selected from the group consisting of (C1-C12)alkylene, -C(CH3)2-, arylene, (C2-C12)alkenylene, heteroarylene, (C3-C8)heterocycloalkylene and (C2-C6)alkynylene; n is 0 or an integer from 1 to 3; E is absent or is selected from -O-, -NR7-, -OC(O)- and -S-; G is arylene or heteroarylene, optionally substituted by one or more substituents selected from the group consisting of halogen atoms, -OH, oxo (=O), -SH, -NO2, -CN, -CON(R6)2, -NH2, -NHCOR6, -CO2R6, (C1-C10)alkylsulfanyl, (C1-C10)alkylsulfinyl, (C1-C10)alkylsulfonyl, (C1-C10)alkyl, aryl, haloaryl, heteroaryl and (C1-C10)alkoxy; R1 and R2 are independently H or selected from the group consisting of (C1-C8)alkyl, (C3-C8)cycloalkyl, (C3-C8)heterocycloalkyl, aryl, heteroaryl, aryl(C1-C6)alkyl, heteroaryl(C1-C6)alkyl and (C3-C8)cycloalkyl(C1-C6)alkyl, optionally substituted by one or more halogen atoms or (C1-C8)alkyl groups or, taken together with the carbon atom to which they are bounded, R1 and R2 6 may form a (C3-C8)cycloalkyl, wherein R1 and R2 are not simultaneously H; M is -O- or -N(R3)-; R3 is H or is selected from the group consisting of (C1-C8)alkyl, (C3-C8)cycloalkyl, aryl and heteroaryl; R4 is a group of formula J1, J2, J3, J4 or J5 R5 is a group of formula K wherein p is 0 or an integer from 1 to 4; q is 0 or an integer from 1 to 4; P is absent or is selected from the divalent group consisting of O, S, SO, SO2, CO, NR6 CH=CH, N(R6)SO2, N(R6)COO, N(R6)C(O), SO2N(R6), CO(O)N(R6) and C(O)N(R6); W is selected from the group consisting of H, (C1-C6)alkyl, (C3-C8)cycloalkyl, aryl and heteroaryl, optionally substituted by one or more substituents selected from the group consisting of halogen atoms, -OH, oxo (=O), -SH, -NO2, -CN, -CON(R6)2, -NH2, -NHCOR6, -CO2R6, (C1-C10)alkylsulfanyl, (C1-C10)alkylsulfinyl, (C1-C10)alkylsulfonyl, (C1-C10)alkyl and (C1-C10)alkoxy; X - is a physiological acceptable anion; R6 is H or is selected from the group consisting of (C1-C10)alkyl, (C1-C6)haloalkyl, (C2-C6)alkynyl, (C2-C6)alkenyl, (C3-C8)cycloalkyl, (C3-C8)cycloalkyl(C1-C6)alkyl, heteroaryl and aryl optionally substituted by 7 one or more substituents selected from the group consisting of halogen atoms, -OH, oxo (=O), -SH, -NO2, -CN, -CONH2, -COOH, (C1-C10)alkoxycarbonyl, (C1-C10)alkylsulfanyl, (C1-C10)alkylsulfinyl, (C1-C10)alkylsulfonyl, (C1-C10)alkyl and (C1-C10)alkoxy; and pharmaceutically acceptable salts or solvates thereof.
The expression “(C1-Cx)alkyl” refers to straight or branched chain alkyl groups wherein the number of carbon atoms is from 1 to x. Examples of groups are methyl, ethyl, n-propyl, isopropyl, t-butyl, pentyl, hexyl, octyl, nonyl, decyl, undecyl, dodecyl and the like.
In an analogous manner, the expression “(C1-Cx)alkylene” refers to divalent groups, such as methylene, ethylene, n-propylene, isopropylene, t-butylene, pentylene, hexylene, octylene, nonylene, decylene, undecylene, dodecylene and the like.
The expression “(C1-C6)haloalkyl” refers to the above “(C1-C6)alkyl” group wherein one or more hydrogen atoms are replaced by one or more halogen atoms, which can be the same or different from each other.
Examples of said (C1-C6)haloalkyl groups include halogenated, poly-halogenated and fully halogenated alkyl groups wherein one or more of the hydrogen atoms are replaced by halogen atoms, e.g. trifluoromethyl group.
The expressions “(C1-C10)alkylsulfanyl”, “(C1-C10)alkylsulfinyl” or “(C1-C10)alkylsulfonyl” refer, respectively, to alkyl-S-, alkyl-SO- or alkyl-SO2- groups.
The expression “hydroxy(C1-C6)alkyl” refers to -alkyl-OH groups.
The expression “(C2-Cx)alkenyl” refers to straight or branched carbon chains with one or more double bonds, wherein the number of carbon atoms is from 1 to x. Examples of said groups comprise ethenyl, propenyl, butenyl, pentenyl, hexenyl, heptenyl, octenyl, nonenyl, decenyl, undecenyl, dodecenyl and the like. 8 In an analogous manner, the expression “(C2-Cx)alkenylene” refers to divalent groups, such as ethenylene, propenylene, butenylene, pentenylene, hexenylene, heptenylene, octenylene, nonenylene, decenylene, undecenylene, dodecenylene and the like.
The expression “(C2-Cx)alkynyl” refers to straight or branched carbon chains with one or more triple bonds, wherein the number of carbon atoms is from 1 to x. Examples of said groups comprise ethynyl, propynyl, butynyl, pentynyl, hexynyl and the like.
In an analogous manner, the expression “(C2-Cx)alkynylene” refers to divalent groups, such as ethynylene, propynylene, butynylene, pentynylene, hexynylene and the like.
The expression “(C1-C10)alkoxy” refers to alkyl-oxy (e.g. alkoxy) groups, being the alkyl portion as above defined. Examples of said groups comprise methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, sec15 butoxy, tert-butoxy, pentoxy, hexoxy and the like.
The expression “(C3-C8)cycloalkyl” refers to mono or bi-cycloaliphatic hydrocarbon groups with 3 to 8 carbon atoms. Examples include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, bicyclo[2.2.1]heptyl and the like.
The expression “(C3-C8)heterocycloalkyl” refers to (C3-C8)cycloalkyl groups, in which at least one ring carbon atom is replaced by a heteroatom or heteroaromatic group (e.g. N, NH, S or O). Examples include quinuclidinyl, pyrrolidinyl, piperidinyl, azabicyclo[3.2.1]octanyl and azoniabicyclo[2.2.2]octanyl and the like.
In an analogous manner, the expressions “(C3-C8)cycloalkylene” and “(C3-C8)heterocycloalkylene” refer to divalent groups, such as, respectively, cyclopropylene, cyclobutylene, cyclopentylene, cyclohexylene, cycloheptylene, bicyclo[2.2.1]heptylene and quinuclidinylene, 9 pyrrolidinylene, piperidinylene, azabicyclo[3.2.1]octanylene, azoniabicyclo[2.2.2]octanylene and the like.
The expression “aryl” refers to mono, bi- or tricyclic ring systems having 5 to 20, preferably from 5 to 15, ring atoms, and wherein at least one ring is aromatic.
The expression “heteroaryl” refers to mono, bi- or tri-cyclic systems with 5 to 20 ring atoms, preferably from 5 to 15, in which at least one ring is aromatic and in which at least one carbon ring atom is a heteroatom or heteroaromatic group (e.g. N, NH, S or O).
Examples of suitable aryl or heteroaryl monocyclic systems include, for instance, thiophene, benzene, pyrrole, pyrazole, imidazole, isoxazole, oxazole, isothiazole, thiazole, pyridine, imidazolidine, furan radicals and the like.
Examples of suitable aryl or heteroaryl bicyclic systems include naphthalene, biphenylene, purine, pteridine, benzotriazole, quinoline, isoquinoline, indole, isoindole, benzothiophene, dihydrobenzo dioxin, dihydro-indene, dihydrobenzo dioxepin, benzo oxazin radicals and the like.
Examples of suitable aryl or heteroaryl tricyclic systems include fluorene radicals as well as benzocondensed derivatives of the aforementioned heteroaryl bicyclic systems.
In an analogous manner, the expressions “arylene” and “heteroarylene” refer to divalent groups, such a phenylene, biphenylene and thienylene.
The expressions “aryl(C1-C6)alkyl”, “heteroaryl(C1-C6)alkyl” and “(C3-C8)cycloalkyl(C1-C6)alkyl” refer to a “(C1-C6)alkyl” respectively substituted by one or more aryl, heteroaryl or (C3-C8)cycloalkyl groups, as defined above.
Examples of aryl(C1-C6)alkyl include triphenylmethyl.
Whenever basic amino or quaternary ammonium groups are present in the compounds of formula I, physiological acceptable anions, selected among chloride, bromide, iodide, trifluoroacetate, formate, sulfate, phosphate, methanesulfonate, nitrate, maleate, acetate, citrate, fumarate, tartrate, oxalate, succinate, benzoate, p-toluenesulfonate, pamoate and naphthalene disulfonate may be present. Likewise, in the presence of acidic groups such as COOH groups, corresponding physiological cation salts may be present as well, for instance including alkaline or alkaline earth metal ions.
It will be apparent that the compounds of general formula I may contain asymmetric centers. Therefore, the invention also includes any of the optical stereoisomers, diastereoisomers and mixtures thereof, in any proportion.
In particular, the carbon atom linked to R1, R2, 10 G and M groups, depending on the meanings provided to R1 and R2 among those formerly reported, may represent a chiral center.
In an embodiment, the configuration is (S).
In another embodiment, the absolute configuration of this chiral center is preferably (R).
In another preferred embodiment, the compounds of general formula I described in the present invention are present as mixtures of diastereoisomers.
In another embodiment, when in the compounds of general formula I, R4 is a group of formula J1, J2 or J5 the carbon atom marked with an asterisk represents a chiral center.
In a preferred embodiment, this chiral center has (R) configuration.
It is to be understood that all preferred groups or embodiments described herebelow for compounds of formula I may be combined among each other and apply as well mutatis mutandis. 11 A first preferred group of compounds is that of general formula I wherein Q is a group of formula Q1, Q2, Q3, Q4, Q5 or Q6.
Z is H or OH; Y is a group of formula Y’ wherein A1 and A2 are, each independently, absent or are selected from the group consisting of (C1-C12)alkylene, (C3-C8)cycloalkylene and (C3-C8)heterocycloalkylene; B is absent or is selected from the group consisting of (C3-C8)cycloalkylene, (C3-C8)heterocycloalkylene, arylene and heteroarylene; C is absent or is selected from the group consisting of -O-, -CO-, -OC(O)-, -C(OO)-, -S-, -S(O)-, -S(O)2- and -N(R7)- wherein R7 is H or is selected from the group consisting of (C1-C8)alkyl, (C3-C8)cycloalkyl, (C3-C8)heterocycloalkyl, aryl, aryl(C1-C8)alkyl, (C1-C8)alkoxy(C1-C8)alkyl and heteroaryl; D is absent or is selected from the group consisting of (C1-C12)alkylene, arylene, (C2-C12)alkenylene, heteroarylene, (C3-C8)heterocycloalkylene and (C2-C6)alkynylene; n is 0; E is absent or is 12 selected from -O-, -NR7- and -S-; G is arylene or heteroarylene, optionally substituted by one or more substituents selected from the group consisting of halogen atoms, -OH, oxo (=O), -SH, -NO2, -CN, -CON(R6)2, -NH2, -NHCOR6, -CO2R6, (C1-C10)alkylsulfanyl, (C1-C10)alkylsulfinyl, (C1-C10)alkylsulfonyl, (C1-C10)alkyl, aryl, haloaryl, heteroaryl and (C1-C10)alkoxy; R1, R2, M, R4 and R6 are as defined above.
Still more preferred within this first group, are the compounds of general formula I, wherein Q is Q1 Z is -OH, A1 is absent or is selected from the group consisting of (C3-C8)heterocycloalkylene and (C1-C12)alkylene, A2 is absent or is selected from the group consisting of (C1-C6)alkylene, B is absent or arylene, C is absent, D is absent or is selected from the group consisting of (C1- C12)alkylene, heteroarylene and arylene, n is 0, E is absent or is -O-, G is arylene optionally substituted by one or more halogen atoms.
Still more preferred within this class, are the compounds of general formula I, wherein A1 is absent or is selected from the group consisting of methylene, ethylene, propylene, butylene, pentylene, hexylene, heptylene, octylene and nonylene, A2 is absent or is selected from the group consisting of methylene and oxadiazolene, B is selected from the group consisting of phenylene and cyclohexylene or is absent, C is absent, D is absent or is selected from methylene, ethylene, propylene, butylene, pentylene, hexylene, heptylene, octylene, nonylene, phenylene and oxadiazolene; n is 0, G is selected from the group consisting of fluoro-biphenylene and phenylene. 13 Even still more preferred within this class are the compounds of general formula I, wherein A1 is selected from the group consisting of ethylene, pentylene, hexylene, heptylene, octylene and nonylene, D is absent, n is 0, R1 is H, R2 is selected from the group consisting of phenyl, biphenyl, naphthyl, pyridinyl, difluorophenyl, methylphenyl, fluorophenyl and thiophenyl, M is -N(H)-, R4 is a group of formula J1 or J3 or J4 or J5 wherein R5 is a group of formula K, wherein p is 0 or 1, P is absent or is CO, q is absent or is 1 and W is H or is selected from the group consisting of (C1-C6)alkyl and aryl. 14 Another class of preferred compounds of general formula I is that wherein Q is Q3 Z is H, A1 is absent or is (C1-C12)alkylene, A2 is absent, B is absent, C is absent, D is absent or (C1-C12)alkylene, E is -O-, G is arylene.
Still more preferred within this class, are the compounds of general formula I, wherein A1 is absent or is selected from the group consisting of methylene, ethylene, propylene, butylene, pentylene, hexylene, heptylene, octylene and nonylene, A2 is absent, B is absent, C is absent, D is absent or is selected from methylene, ethylene, propylene, butylene, pentylene, hexylene, heptylene, octylene and nonylene; n is 0, G is phenylene.
Even still more preferred within this class, are the compounds of general formula I, wherein A1 is nonylene, A2, B and C are absent, D is a absent, n is 0, R1 is H, R2 is phenyl, M is -N(H)- and R4 is J1.
Another preferred group of compounds is that of general formula I wherein R1 and R2 are independently H or selected from the group consisting of (C1-C8)alkyl, (C3-C8)cycloalkyl, (C3-C8)heterocycloalkyl, aryl, heteroaryl, aryl(C1-C6)alkyl, heteroaryl(C1-C6)alkyl and (C3-C8)cycloalkyl(C1-C6)alkyl, optionally substituted by one or more halogen atoms or (C1-C8)alkyl groups or, taken together with the carbon atom they are linked to, R1 and R2 may form a (C3-C8)cycloalkyl group, wherein R1 and R2 are not simultaneously H; M is -O- or -N(R3)-; R3 is H or is selected from the group consisting of (C1-C8)alkyl, (C3-C8)cycloalkyl, aryl and heteroaryl; R4 is a group of formula J1, J2, J3, J4 or J5 R5 is a group of formula K wherein p is 0 or an integer from 1 to 4; q is 0 or an integer from 1 to 4; P is absent or is selected from the group consisting of -O-, -S-, -S(O)-, -S(O2)-, -C(O)-, -N(R6)-, -CH=CH-, -N(R6)S(O2)-, -N(R6)CO(O)-, -N(R6)C(O)-, -SO2N(R6)-, -CO(O)N(R6)- and -C(O)N(R6)-; W is selected from the group consisting of (C1-C6)alkyl, (C3-C8)cycloalkyl, aryl and heteroaryl, optionally substituted by one or more substituents selected from the group consisting of halogen atoms, -OH, oxo (=O), -SH, -NO2, -CN, -CON(R6)2, -NH2, -NHCOR6, -CO2R6, (C1-C10)alkylsulfanyl, (C1-C10)alkylsulfinyl, (C1-C10)alkylsulfonyl, (C1-C10)alkyl and (C1-C10)alkoxy; R6 is selected from the group consisting of H, (C1-C10)alkyl, (C1-C6)haloalkyl, (C3-C8)cycloalkyl, heteroaryl and aryl; G, Y, Z and Q are as defined above.
Still more preferred within this class, are the compounds of general formula I wherein R1 and R2 are independently H or selected from the group consisting of (C1-C8)alkyl, (C3-C8)cycloalkyl, aryl and heteroaryl, optionally substituted by one or more halogen atoms or (C1-C8)alkyl groups or, taken together with the carbon atom to which they are bounded, R1 and R2 may form a (C3-C8)cycloalkyl group, wherein R1 and R2 are not simultaneously H; M is -N(R3)-; R3 is H; R4 is a group of formula J1 16 or J3 or J4 wherein R5 is a group of formula K, wherein p is 0, P is absent, q is 1 and W is H or is selected from the group consisting of (C1-C6)alkyl and aryl.
Still more preferred within this class are the compounds of general formula I wherein W is H or phenyl; R1 is H, R2 is selected from the group consisting of phenyl, biphenyl, naphthyl, thiophenyl, pyridinyl, difluorophenyl, methylphenyl and fluorophenyl; M is -N(H)-; R4 is selected from the group consisting of quinuclidinyl, benzylpiperidinyl, methylpiperidinyl, benzylazabicyclo[3.2.1]octanyl and azoniabicyclo[2.2.2]octanyl.
A second group of preferred compounds is that of general formula I wherein Q is a group of formula Q1, Q2, Q3, Q4, Q5 or Q6. 17 Z is H or OH; Y1 is a group of formula Y1 wherein A1 is (C1-C12)alkylene; C is absent or is selected from the group consisting of -O-, -CO-, -OC(O)- or is a group of formula C1-C18 18 wherein R7 is H or is selected from the group consisting of linear or branched (C1-C8)alkyl, (C3-C8)cycloalkyl, (C3-C8)heterocycloalkyl, aryl, (C1-C6)arylalkyl, (C1-C6)alkoxy(C1-C6)alkyl and heteroaryl and R8 is (C1-C8)alkoxycarbonyl; B is absent or is selected from the group consisting of (C3-C8)cycloalkylene, arylene and heteroarylene, optionally substituted by one or more groups selected from halogens, nitrile, (C1-C6)alkyl, (C1-C6)alkoxy and aryl(C1-C6)alkyl; D is absent or is selected from the group consisting of (C1-C12)alkylene, -C(CH3)2-, heteroarylene and arylene; n is 0 or an integer from 1 to 2; E is -O-; G is arylene or heteroarylene, optionally substituted by one or more substituents selected from the group consisting of halogen atoms, -OH, oxo (=O), -SH, -NO2, -CN, -CON(R6)2, -NH2, -NHCOR6, -CO2R6, (C1-C10)alkylsulfanyl, (C1-C10)alkylsulfinyl, (C1-C10)alkylsulfonyl, (C1-C10)alkyl, aryl, haloaryl, heteroaryl and (C1-C10)alkoxy; R1, R2, M and R4 are as defined above.
Still more preferred within this second group, are the compounds of general formula I, wherein Q is Q1 Z is -OH, A1 is selected from (C1-C12)alkylene and (C3-C8)heterocycloalkylene; C is absent or is selected from the group consisting of -O-, -CO-, -OC(O)-, C11, C13, C14, C16, C17, C18 wherein R7 is H or linear or branched (C1-C8)alkyl, C7 wherein R7 is H and C15 wherein R8 is (C1-C8)alkoxycarbonyl; B is absent or is selected from the group consisting of (C3-C8)cycloalkylene, (C3-C8)heterocycloalkylene, arylene and heteroarylene, optionally substituted by one or more halogens; D is absent or 19 is selected from the group consisting of (C1-C12)alkylene, -C(CH3)2-, arylene and heteroarylene; n is 0 or an integer from 1 to 2; E is -O-; G is arylene, optionally substituted by one or more substituents selected from the group consisting of halogen atoms, aryl and heteroaryl.
Still more preferred within this class, are the compounds of general formula I, wherein A1 is selected from the group consisting of methylene, ethylene, propylene, butylene, pentylene and hexylene; C is absent or is selected from the group consisting of -O-, -CO-, -OC(O)-, C11, C13, C14, C16, C17, C18 wherein R7 is H or is selected from the group consisting of methyl, ethyl, isopropyl and C15 wherein n is 0 or 1 and R8 10 is ethoxycarbonyl; B is absent or is selected from phenylene, piperidinylene, cyclopropylene, cyclohexylene, piridinediyl, furanediyl and oxazolediyl, optionally substituted by one or more halogens; D is absent or is selected from methylene, -C(CH3)2- , phenylene and oxadiazolylene; n is 0 or an integer from 1 to 2; E is -O-; G is selected from phenylene and biphenylene, optionally substituted by one or more substituents selected from the group consisting of fluorine, phenyl and 2-thiophenyl.
Even still more preferred within this class are the compounds of general formula I, wherein A1 is selected from the group consisting of methylene, ethylene, propylene, butylene, pentylene and hexylene; C is absent or is selected from the group consisting of -O-, -CO-, -OC(O)-, C11, C13, C14, C16, C17, C18 wherein R7 is H or is selected from the group consisting of methyl, ethyl and isopropyl and C15 wherein n is 0 or 1 and R8 is ethoxycarbonyl; B is absent or is selected from phenylene, piperidinylene, cyclopropylene, cyclohexylene, piridinediyl, furanediyl and oxazolediyl, optionally substituted by one or more halogens; D is absent or is selected from methylene, -C(CH3)2-, phenylene and oxadiazolylene; n is 0 or an integer from 1 to 2; E is -O-; G is selected from phenylene and biphenylene, optionally substituted by one or more substituents selected from the group consisting of fluorine, phenyl and 2-thiophenyl; R1 is H, R2 is selected from the group consisting of phenyl, cyclohexyl, fluorophenyl and chlorophenyl, M is -N(H)-, R4 is a group of formula J1 or J3 or J4 or J5 wherein R5 is a group of formula K wherein p is 0 or 1, P is absent or is CO, q is absent or is 1 and W is H or is selected from the group consisting of (C1-C6)alkyl and aryl. 21 Even still more preferred within this class, are the compounds of general formula I, wherein A1 is selected from the group consisting of methylene, ethylene, propylene, butylene, pentylene and hexylene; C is absent or is selected from the group consisting of -O-, -CO-, -OC(O)-, C11, C13, C14, C16, C17 and C18 wherein R7 is H or is selected from the group consisting of methyl, ethyl and isopropyl and C15 wherein n is 0 or 1 and R8 is ethoxycarbonyl; B is absent or is selected from phenylene, piperidinylene, cyclopropylene, cyclohexylene, piridinediyl, furanediyl and oxazolediyl, optionally substituted by one or more halogens; D is absent or is selected from methylene, -C(CH3)2-, phenylene and oxadiazolylene; n is 1; E is -O-; G is phenylene optionally substituted by one or more substituents selected from the group consisting of phenyl and 2-thiophenyl; R1 is H, R2 is selected from the group consisting of phenyl, cyclohexyl, fluorophenyl and chlorophenyl, M is -N(H)-, R4 is a group of formula J1 or J5, wherein R5 is a group of formula K, wherein p is 0 or an integer from 1 to 4; q is 0 or an integer from 1 to 4; P is absent or is selected from the group consisting of -O- and -C(O)-; W is aryl; G, Y, Z and Q are as defined above.
Also described is a process for the preparation of the compounds of general formula I, which process comprises the reaction of a compound of general formula XIX with a compound of general formula XX 22 Also described is a process for the preparation of the compounds of general formula I which process comprises the reaction of a compound of general formula XXVII with a compound of formula XXIX under the transition metal catalyzed cross-coupling reaction condition.
Also described is a process for the preparation of the compounds of general formula I, which process comprises the reaction of a compound of general formula XXIV with a compound of formula XXX 23 Also described is a process for the preparation of the compounds of general formula I wherein R4 is J5 J5 this process comprising the reaction of the corresponding tertiary amine precursor of formula I wherein R5 is a J1-J4 group with a compound of formula XXXI Also described is a process for the preparation of the compounds of general formula I wherein M is –NR3-, this process comprising the treatment of a compound of general formula XV with a compound of general formula XVII 24 Also described is a process for the preparation of the compounds of general formula I wherein M is –NR3-, this process comprising the treatment of a compound of general formula XXXIX with a compound of general formula XL followed by removal of the protecting group (PG) Also described is a process for the preparation of a compound of general formula XXXIV in its two enantiomeric forms, by mean of crystallization of the corresponding diastereomeric salt, obtained by salification of the racemic mixture with an enantiomerically pure carboxylic acid.
The present invention also provides pharmaceutical compositions of compounds of formula I alone or in combination with or in admixture with one or more pharmaceutically acceptable carriers and/or excipients.
The present invention also provides the use of compounds of formula I for preparing a medicament.
In a further aspect, the invention provides the use of compounds of formula I for the prevention and/or treatment of any broncho-obstructive or inflammatory disease, preferably asthma or chronic bronchitis or chronic obstructive pulmonary disease (COPD).
In a further aspect, the invention provides the use of compounds of formula I for the manufacture of a medicament for the prevention and/or treatment of any broncho-obstructive or inflammatory disease, preferably asthma or chronic bronchitis or chronic obstructive pulmonary disease (COPD).
Also described is a method for prevention and/or treatment of any broncho-obstructive or inflammatory disease, preferably asthma or chronic bronchitis or chronic obstructive pulmonary disease (COPD), which comprises administering to a subject in need thereof a therapeutically effective amount of a compound of general formula I.
The present invention also provides pharmaceutical compositions suitable for administration by inhalation.
Inhalable preparations include inhalable powders, propellant-containing metering aerosols or propellant-free inhalable formulations.
The invention is also directed to a device which may be a single- or multi-dose dry powder inhaler, a metered dose inhaler and a soft mist nebulizer comprising the compounds of formula I.
Also described is a kit comprising the pharmaceutical compositions of compounds of formula I alone or in combination with or in admixture with one or more pharmaceutically acceptable carriers and/or excipients and a device which may be a single- or multi-dose dry powder inhaler, a metered dose inhaler and a soft mist nebulizer comprising the compounds of general formula I.
According to specific embodiments, the present invention provides the compounds reported below: 26 Cpd Chemical Name 1 (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)- (phenyl)methylcarbamate 2 (R)-quinuclidinyl (3-(8-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)octyloxy)phenyl)- (phenyl)methylcarbamate 3 (R)-quinuclidinyl(3-(7-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)heptyloxy)phenyl)- (phenyl)methylcarbamate 4 (R)-quinuclidinyl (3-(6-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)hexyloxy)phenyl)- (phenyl)methylcarbamate (R)-quinuclidinyl (3-(5-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)pentyloxy)phenyl)- (phenyl)methylcarbamate 6 1-benzylpiperidinyl (3-(9-((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethylamino)nonyloxy)phenyl)- (phenyl)methylcarbamate 7 1-methylpiperidinyl (3-(9-((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethylamino)nonyloxy)phenyl)- (phenyl)methylcarbamate 8 8-benzylazabicyclo[3.2.1]octanyl (3-(9-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)nonyloxy)phenyl)-(phenyl)methylcarbamate 9 (R)-quinuclidinyl (4-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)- (phenyl)methylcarbamate (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(thiophen yl)methylcarbamate 11 (R)-quinuclidinyl biphenylyl(3-(9-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)nonyloxy)phenyl)-methylcarbamate 12 (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(naphthalen yl)methylcarbamate 13 (R)-quinuclidinyl biphenylyl(3-(9-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)nonyloxy)phenyl)-methylcarbamate 14 (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(pyridin yl)methylcarbamate (continued) 27 (R)-quinuclidinyl (3,5-difluorophenyl)(3-(9-((R)hydroxy (8-hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)nonyloxy)- phenyl)methylcarbamate 16 (R)-quinuclidinyl (3,4,5-difluorophenyl)(3-(9-((R)hydroxy (8-hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)nonyloxy)- phenyl)methylcarbamate 17 (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(o-tolyl)- methylcarbamate 18 (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(m-tolyl)- methylcarbamate 19 (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(p-tolyl)- methylcarbamate (R)-quinuclidinyl (4-difluorophenyl)(3-(9-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)- nonyloxy)phenyl)methylcarbamate 1B (R)-quinuclidinyl (3-fluorophenyl)(3-(9-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)nonyloxy)phenyl)methylcarbamate 2B (R)-quinuclidinyl (3-chlorophenyl)(3-(9-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)nonyloxy)phenyl)methylcarbamate 1C (R)-quinuclidinyl (cyclohexyl(3-((9-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)nonyl)oxy)phenyl)methyl)carbamate 2C (R)-quinuclidinyl ((3-((6-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(thiophen2-yl)methyl)carbamate 3C (R)-quinuclidinyl ((3-((6-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(thiophen3-yl)methyl)carbamate 21 (R)-quinuclidinyl (3-(9-(2-(4-hydroxyoxo-2,3- dihydrobenzo[d]thiazolyl)ethylamino)nonyloxy)- phenyl)(phenyl)methylcarbamate 22 (R)-quinuclidinyl (3-(4-(2-((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethylamino)ethyl)benzyloxy)- phenyl)(phenyl)methylcarbamate 23 (R)-quinuclidinyl (3-(2-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin yl)ethylamino)ethyl)phenyl)(phenyl)methylcarbamate (continued) 28 24 (3R)((3-(6-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)hexyloxy)phenyl)(phenyl)- methylcarbamoyloxy)(2-oxophenylethyl) azoniabicyclo[2.2.2]octane 3B (R)-quinuclidinyl (3-(3-(2-((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethylamino)ethyl)benzyloxy)phenyl)- (phenyl)methylcarbamate formate 4B (3R)((((3-((4-(2-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)ethyl)benzyl)oxy)-phenyl)- (phenyl)-methyl)carbamoyl)oxy)(2-oxo phenylethyl)quinuclidinium 5B (3R)((((3-chlorophenyl)(3-((9-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)- methyl)-carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 6B (3R)((((3-bromo((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 7B (R)-quinuclidinyl (2-chloro(9-((R)hydroxy(8-hydroxy2-oxo-1,2-dihydroquinolinyl)ethylamino)nonyloxy)phenyl)- (phenyl)methylcarbamate 8B (R)-quinuclidinyl ((2,6-difluoro((9-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)carbamate 9B (R)-quinuclidinyl ((2-bromo((9-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)nonyl)oxy)phenyl)-(phenyl)methyl)carbamate 10B (3R)((((2-chloro((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 11B (3R)((((2,6-difluoro((9-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 12B (3R)((((2-bromo((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 13B (3R)((((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)methylphenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 14B (R)-quinuclidinyl ((3-((9-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy) methoxyphenyl)(phenyl)methyl)carbamate 15B (R)-quinuclidinyl ((3-((9-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy) methoxyphenyl)(phenyl)methyl)carbamate (continued) 29 16B (3R)((((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)methoxyphenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 17B (3R)((((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)methoxyphenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 18B (3R)((((5-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)-[1,1'-biphenyl] yl)(phenyl)methyl)carbamoyl)oxy)(2-oxo phenylethyl)quinuclidinium 19B (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)(thiophen yl)phenyl)(phenyl)methylcarbamate 20B (3R)((((3-((3-(4-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)butoxy)benzyl)oxy)- phenyl)(phenyl)-methyl)carbamoyl)oxy)(2-oxo phenylethyl)quinuclidinium 21B (3R)((((3-((3-(4-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)butoxy)benzyl)oxy)- phenyl)(phenyl)-methyl)carbamoyl)oxy)(2- phenoxyethyl)quinuclidinium 22B (3R)((((3-((3-((5-(((R)hydroxy(8-hydroxyoxo-1,2- dihydro-quinolinyl)ethyl)amino)pentyl)oxy)benzyl)oxy)phenyl)- (phenyl)-methyl)carbamoyl)oxy)(2-oxo phenylethyl)quinuclidinium 23B (3R)((((3-((3-((5-(((R)hydroxy(8-hydroxyoxo-1,2- dihydro-quinolinyl)ethyl)amino)pentyl)oxy)benzyl)oxy)- phenyl)(phenyl)-methyl)carbamoyl)oxy)(2- phenoxyethyl)quinuclidinium 24B (R)-quinuclidinyl (3-fluorophenyl)(3-(6-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyloxy)phenyl)methylcarbamate 25B (3R)((((3-((5-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)pentyl)oxy)phenyl)(phenyl)- methyl)carbamoyl)oxy)(4-phenylbutyl)quinuclidinium 26B (R)-Quinuclidinyl (3-fluorophenyl)(3-(3-(2-((R)hydroxy (8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)ethyl)benzyloxy)phenyl)methylcarbamate 27B (3R)((((3-fluorophenyl)(3-((3-(2-(((R)hydroxy(8-hydroxy2-oxo-1,2-dihydroquinolin yl)ethyl)amino)ethyl)benzyl)oxy)phenyl)-methyl)carbamoyl)oxy)- 1-(2-oxophenylethyl)quinuclidinium (continued) 28B (3R)((((3-((4-((((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)methyl)benzyl)oxy)-phenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 29B (R)-Quinuclidinyl (3-((4'-(2-((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethylamino)ethyl)biphenyl yl)methoxy)phenyl)(phenyl)methylcarbamate 30B (R)-quinuclidinyl ((3-((4-((4-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)butyl)carbamoyl)- benzyl)-oxy)phenyl)(phenyl)methyl)carbamate 31B (R)-quinuclidinyl (3-(4-(3-((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethylamino)propylcarbamoyl)benzyloxy)- phenyl)(phenyl)methylcarbamate 32B (3R)((((3-((4-((3-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)propyl)carbamoyl)benzyl)oxy)- phenyl)(phenyl)methyl)carbamoyl)oxy)(2-oxo phenylethyl)quinuclidinium 33B 4-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 34B -((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)pentyl 4-((3-(phenyl(((R)-quinuclidin yloxy)carbonylamino)methyl)phenoxy)methyl)benzoate 35B 6-((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyl 4-((3-(phenyl(((R)-quinuclidin yloxy)carbonylamino)methyl)phenoxy)methyl)benzoate 4C 7-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)heptyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 5C 4-((((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)methyl)benzyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 6C 4-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethyl)phenyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 7C 4-((((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)methyl)phenyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 8C 4-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethyl)benzyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 36B (3R)((((3-((4-(1-((4-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)butoxy)carbonyl)cyclopropyl)- benzyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)(2-oxo phenylethyl)quinuclidinium (continued) 31 37B (R)-quinuclidinyl (3-(2-(3'-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethylamino)methyl)biphenyl yl)ethoxy)phenyl)(phenyl)methylcarbamate 38B (R)-quinuclidinyl (3-(2-(3'-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethylamino)methyl)biphenyl yl)ethoxy)phenyl)(phenyl)methylcarbamate 39B 6-((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyl 2-(3-(phenyl(((R)-quinuclidin yloxy)carbonylamino)methyl)phenoxy)acetate 40B (R)-quinuclidinyl ((3-((6-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)- (phenyl)methyl)carbamate 41B (R)-quinuclidinyl ((3-((6-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)- (phenyl)methyl)carbamate 42B (3R)((((3-((6-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(phenyl)- methyl)-carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 43B (3R)((((3-((6-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(phenyl)- methyl)-carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 44B 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 45B 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 9C -(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl 2-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)acetate 10C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)acetate 11C -(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl 2-methyl(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)propanoate 12C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-methyl(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)propanoate 13C -(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl 2,2-dimethyl(3-(phenyl((((R)-quinuclidin3-yloxy)carbonyl)amino)methyl)phenoxy)propanoate (continued) 32 14C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolinyl)- ethyl)amino)butyl 1-(2-(3-(phenyl((((R)-quinuclidinyloxy)- carbonyl)amino)methyl)phenoxy)acetyl)piperidinecarboxylate 15C 4-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethyl)benzyl 2-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)acetate 16C (R)-quinuclidinyl ((3-((9-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy) methylphenyl)(phenyl)methyl)carbamate 17C (R)-Quinuclidinyl ((3-bromo((9-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)- oxy)phenyl)(phenyl)methyl)carbamate 18C (R)-quinuclidinyl ((5-((9-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)-[1,1'-biphenyl]- 3-yl)(phenyl)methyl)carbamate 19C (R)-quinuclidinyl ((2-bromo((9-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)- phenyl)(phenyl)methyl)carbamate 20C (R)-quinuclidinyl ((3'-fluoro((9-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)- [1,1'-biphenyl]yl)(phenyl)methyl)carbamate 21C (R)-quinuclidinyl ((3-((3-(4-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)butoxy)benzyl)- oxy)phenyl)(phenyl)methyl)carbamate 22C (R)-quinuclidinyl ((3-((3-((5-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)pentyl)oxy)benzyl)- oxy)phenyl)(phenyl)methyl)carbamate 23C (3R)(((cyclohexyl(3-((9-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 24C (3R)((((3-((6-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(thiophen yl)methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidin ium 25C (3R)((((3-fluorophenyl)(3-((6-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)- methyl)-carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 26C (3R)((((3-((6-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(thiophen yl)methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 27C (3R)((((3-((4-((4-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)butyl)carbamoyl)benzyl)oxy)- phenyl)(phenyl)methyl)carbamoyl)oxy)(2-oxo phenylethyl)quinuclidinium (continued) 33 28C (3R)((((3-((7-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)heptyl)oxy)phenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 29C (3R)((((3-((7-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)heptyl)oxy)phenyl)(phenyl)- methyl)-carbamoyl)oxy)(3-phenylpropyl)quinuclidinium 30C (3R)((((3-((5-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)pentyl)oxy)phenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 31C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolinyl)- ethyl)amino)butyl 1-(4-((3-(phenyl((((R)-quinuclidinyloxy)- carbonyl)amino)methyl)phenoxy)methyl)phenyl)cyclopentanecarboxylate 32C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolinyl)- ethyl)amino)butyl 1-(4-((3-(phenyl((((R)-quinuclidinyloxy)- carbonyl)amino)methyl)phenoxy)methyl)phenyl)cyclohexane-carboxylate 33C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-methyl(4-((3-(phenyl((((R)-quinuclidin3-yloxy)carbonyl)amino)methyl)phenoxy)methyl)- phenyl)propanoate 34C 8-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)octyl 3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzoate 35C 9-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)nonyl 3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzoate 36C 7-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)heptyl 3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzoate 37C 6-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)hexyl 3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzoate 38C -(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl 3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzoate 39C 4-((4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl)carbamoyl)benzyl 3-(phenyl((((R)- quinuclidinyloxy)carbonyl)amino)methyl)benzoate 40C 4-(N-(4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin5-yl)ethyl)amino)butyl)sulfamoyl)benzyl 3-(phenyl((((R)- quinuclidinyloxy)carbonyl)amino)methyl)benzoate 41C 4-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethyl)benzyl 3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzoate (continued) 34 42C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzamido)methyl)benzoate 43C (2S)(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin5-yl)ethyl)amino)butyl 3-phenyl(4-((3-(phenyl((((R)- quinuclidinyloxy)carbonyl)amino)methyl)phenoxy)methyl)- benzamido)propanoate 44C (R)-quinuclidinyl ((3-((3-(4-(2-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)ethyl)phenyl)-1,2,4- oxadiazolyl)methoxy)phenyl)(phenyl)methyl)carbamate 45C (R)-quinuclidinyl ((5-((9-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)pyridin yl)(phenyl)methyl)carbamate 46C (R)-quinuclidinyl ((3-fluorophenyl)(5-((9-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)nonyl)oxy)pyridinyl)methyl)carbamate 47C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-chloro((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 48C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-fluoro((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 49C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 6-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)nicotinate 50C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 5-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)furancarboxylate 51C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)oxazole carboxylate 52C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 3-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 53C -(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl 2-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)acetate 54C -(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl 2-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)acetate 55C -(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)hexyl 2-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)acetate (continued) 56C -(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)hexyl 2-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)acetate 57C (R)-quinuclidinyl ((3-((4-((3-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)propyl)carbamoyl)- benzyl)oxy)phenyl)(phenyl)methyl)carbamate 58C (R)-quinuclidinyl ((3-((4-((3-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)ethyl)carbamoyl)- benzyl)oxy)phenyl)(phenyl)methyl)carbamate 59C (R)-quinuclidinyl ((3-((4-(ethyl(3-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)propyl)- carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate 60C (R)-quinuclidinyl ((3-((4-((3-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)propyl)(methyl)- carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate 61C (R)-quinuclidinyl ((3-((4-((3-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)propyl)(isopropyl)- carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate 62C (1R,4R)(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)butyl 4-((4-((3-(phenyl((((R)- quinuclidinyloxy)-carbonyl)amino)methyl)phenoxy)methyl)- benzamido)methyl)-cyclohexanecarboxylate 63C (2S)-methyl 4-((2-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)ethyl)(methyl)amino)oxo (4-((3-(phenyl((((R)-quinuclidinyloxy)carbonyl)amino)methyl)- phenoxy)methyl)benzamido)butanoate 64C ((1R,4R)((((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)methyl)cyclohexyl)methyl 4-((3- (phenyl-(((quinuclidinyloxy)carbonyl)amino)methyl)phenoxy)- methyl)benzoate 65C 2-((4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl)amino)oxoethyl 4-((3-(phenyl((((R)- quinuclidinyloxy)carbonyl)amino)methyl)phenoxy)- methyl)benzoate 66C 2-((3-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)propyl)amino)oxoethyl 4-((3-(phenyl((((R)- quinuclidinyloxy)carbonyl)amino)methyl)phenoxy)- methyl)benzoate 67C 2-(4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butoxy)oxoethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)-methyl)benzoate 68C 2-((5-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl)oxy)oxoethyl 4-((3-(phenyl((((R)-quinuclidin3-yloxy)carbonyl)amino)methyl)phenoxy)-methyl)benzoate (continued) 36 69C 2-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethoxy)ethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 70C 2-(4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butoxy)ethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 71C 2-((5-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl)oxy)oxoethyl 4-((3-(phenyl((((R)-quinuclidin3-yloxy)carbonyl)amino)methyl)-phenoxy)methyl)benzoate 72C 2-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethoxy)ethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 73C 2-(4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butoxy)ethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 74C 3-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethyl)benzyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 75C 3-(3-(phenyl((((R)-quinuclidinyloxy)carbonyl)amino)methyl)- phenoxy)propyl 4-(2-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)ethyl)benzoate 76C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-(2-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)ethyl)benzoate 77C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolinyl)- ethyl)amino)butyl 4-(5-((3-(phenyl((((R)-quinuclidinyloxy)- carbonyl)amino)methyl)phenoxy)methyl)-1,2,4-oxadiazolyl)benzoate 78C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-((4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)piperidin yl)methyl)benzoate 79C 2-(4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butoxy)ethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 80C 4-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethyl)benzyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 81C 2-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethoxy)ethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 82C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-chloro((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 83C 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-fluoro((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 37 The compounds of the invention can be prepared from readily available starting materials using the following general methods and procedures or by using other information readily available to those of ordinary skill in the art.
Although a particular embodiment of the present invention may be shown or described herein, those skilled in the art will recognize that all embodiments or aspects of the present invention can be prepared using the methods described herein or by using other methods, reagents and starting materials known to those skilled in the art. It will also be appreciated that where typical or preferred process conditions (i.e., reaction temperatures, times, mole ratios of reactants, solvents, pressures, etc.) are given, other process conditions can also be used unless otherwise stated. While the optimum reaction conditions may vary depending on the particular reactants or solvent used, such conditions can be readily determined by one skilled in the art by routine optimisation procedures.
Compounds of general formula I may be prepared according to the following synthetic Scheme.
Scheme O LG O R4 E G O R2 E G O R2 R1 MgBr E A1B C D O O G O R2 A1B A2 DE O E = O,S O D= alkylene D= alkylene D= alkenylene or alkynylene E=bond Br G O H Reduction E G R1 OH D= alkylen R2 R4 HO H H D= alkenylene or alkynylene E=bond R1 MgBr H E = O,S II E = O,S II III IV VI VII VIII X V V XI XIII XIV XV XVI XII XVII VI IX 1) ACN 2) Hydrolysis R1 MgBr VI Reduction Reduction Reduction E G O O H Alkyl R1 R2 MgBr MgBr A B C D E O O G O O R1 R2 MgBr MgBr Alkyl (CH2)n A2 (CH2 A1B C D )n O O A2 E A1B C D O O G O R2 A2 E A1B C D O O A2 H E A1B C D O O G OH R1 A2 R2 (CH2 A1B C D )n O O A2 E A1 B C D O O G N3 A R1 2 R2 E A1 B C D O O G NH R1 A2 R2 R3 O LG O R4 X VIII E A1 B C D O O G M A2 R1 R2 O O R4 OH OH LG (CH2)n (CH2)n (CH2)n (CH2)n (CH2)n (CH2)n (CH2)n (CH2)n XVII 38 H N Y G R1 M R2 O O R4 Q NH2 Z Q Z H N Y G R1 M R2 O O Q Z R5 LG Q O NH Q Z H2N PG PG N Q Z PG A1B A2C D E G R1 N R2 R3 O O H E R4 G R1 N R2 R3 O O A B C D Br R4 O E H I XVIII XIX XX XXI XXII XXV I R4= XXIII XXIV XXVI XXVII XXVIII XXIX R4 XXX XXXI N + R5 E D A1 B O O G M R1 R2 O O R4 A1 B C D E O G M R1 A2 R2 O O R4 H N Q Z PG A1B A2C D (CH2)n O A1 B A2 C D (CH2)n LG A1 B A2 C D E H LG A1B A2C D (CH2)n H E G O R2 II E=O,S 1) formamide 2) H+ H E G NH2 R2 XXXII E=O,S E G N R H 2 XXXIII E=O,S PG E G N R H 2 XXXIV PG H D A1 B C D O O A2 (CH2)n III HO2C A1 B C D E O O G NH R1 A2 R2 PG N Q Z PG A1B A2OH D E G M R1 R2 O O HO2C R4 A1 B OH O O A2 O O R4 LG 1) deprotection 2) O O R4 LG 1) deprotection 2) LG Q Z H N A1B A2C D (CH2)n PG LG (CH2)n (CH2 (CH2)n )n (CH2)n (CH2)n (CH2)n LG LG LG LG (CH2)n (CH2)n XXXV XXXVI XXXVII XXXVIII XXXIX Base 1) 2) R2MgBr or R2Li 3) H+ H2N S tBu O HO2C D (CH2)n LG XL XVII XVII XLI C A2 39 40 General procedure for the preparation of compounds of formula I The compounds of general formula IX represent a compound wherein A1 is alkylene, cycloalkylene or heterocycloalkylene substituted with oxo, leading to an aldehyde or ketone protected as cyclic acetal. The cyclic acetal protecting group (PG) can be removed leading to a compound of general formula XXVI.
In the case A1 is absent and B is a cycloalkylene, heterocycloalkylene or a group of formula B1, the carbonyl moiety, as such or protected, must be considered on group B.
The synthesis of compounds of general formula I may require the protection of potential reactive functionality in addition to those methods already described. In such a case, examples of compatible protecting groups (PG) and their particular methods of protection and deprotection are described in “Protecting groups in organic Synthesis” by T.W. Green and P. Wutz (Wiley-Interscience publication, 1999). Compounds of general formula I can be prepared for example by reaction of a compound of general formula XIX with a compound of general formula XX. This reductive amination reaction can be performed following several different protocols described in the literature and well known for those skilled in the art. For example, it can be performed in solvent such as methanol, ethanol, tetrahydrofuran (THF) or dichloromethane (DCM) using a reducing agent such as NaBH4, NaCNBH3 or NaBAcO3H. It could be useful to obtain the imine before adding the reducing agent. The reaction proceeds smoothly at room temperature (RT) over 1 to 12 hours.
The intermediate of general formula XIX can be easily prepared by reaction of a compound of general formula XIV with a compound of general formula XVII. The reaction occurs smoothly at RT or lower temperature in a solvent such as DCM or pyridine over 1-16 hours leading to compounds of 41 formula XVIII, that can be easily deprotected in aqueous acidic solution, leading to a compound of general formula XIX.
Compounds of general formula XVII are either commercially available or can be prepared by reacting an alcohol of general formula XVI with for example diphosgene in a solvent such as DCM, THF or acetonitrile (ACN) at RT or lower temperature, over a period of time ranging from 0.5 to 12 hours, leading to a compound of general formula XVII wherein the leaving group LG is chlorine. Alternatively alcohol of general formula XVI can be reacted with for example carbonyldiimidazole (CDI) leading to the same intermediate wherein LG is imidazole. Other possible intermediates with other known LGs can be prepared as described in the literature.
Compound of general formula XV, wherein R3 is hydrogen, may be prepared from a compound of general formula XII via Ritter reaction (acetonitrile and sulphuric acid at RT) followed by hydrolysis of the intermediate acetamide performed under basic condition.
Alternatively compounds of general formula XV can be prepared by reduction of azide formula XIV via hydrogenation under hydrogen atmosphere or hydrogen transfer conditions. The reaction occurs in alcohols at RT or higher temperature and stops in 1 to 12 hours. An alternative reduction method could be the Staudinger reaction, which involves treatment of the azide, first with for example triphenylphosphine, followed by hydrolysis of the iminophosphorane intermediate with water. This reaction occurs at RT in a water miscible solvent such as for example THF. The use of a strong reducing agent such as for example LiAlH4 in THF or ether at -40ºC or lower temperature could easily allow to perform the required conversion of compound XIV into XV.
Azide XIV is obtained from compound of formula XII by reaction with diphenyl phosphoryl azide. The reaction is performed in a high boiling point 42 such as toluene or xylene in the presence of a strong base such as, but not limited to 1,8-diazabicyclo[5.4.0]undecene (DBU) at a temperature ranging from 80 to 120ºC and it completes over 12 to 24 hour. Alternatively the hydroxyl moiety of intermediate of formula XII can be converted into a suitable leaving group (LG), such as for example mesyl, tosyl or halogen and then reacted with an alkaline azide in a polar solvent such as acetonitrile, DMF or N-Methylpyrrolidone (NMP) at RT or higher temperature.
Compounds of general formula XV wherein R3 is alkyl, can be prepared from compounds of formula XV wherein R3 is hydrogen, by reductive amination with a suitable aldehyde or ketone. The reaction can be conducted under the same reaction conditions described for the preparation of compounds of formula I from compounds of formula XIX and XX.
Alternatively the alkylation of amine with alkyl halides, alkyl tosylates or mesylates under standard reaction conditions, well known to those skilled in the art, can be considered to achieve the described conversion.
Compounds of general formula I wherein M is -O-, can be prepared treating a compound of general formula XII with a compound of general formula XVII. The reaction occurs in an aprotic solvent such as THF, DCM or DMF and requires the use of a strong base such as alkyl lithium or sodium hydride. It proceeds rapidly at 0°C or lower temperature over a period of time ranging from 1 to 12 hours. The reaction can be performed using the compound of general formula XVII or alternatively the analogue compound in which the chlorine atom is substituted with another usual leaving group, such as imidazole or p-nitro phenol, typical reactant for the preparation of organic asymmetric carbonates or carbamates.
Intermediates of general formula XII can be prepared in several different ways. For example they can be prepared from reaction of a compound of general formula VII, wherein E is -O- or -S-, and an aldehyde of 43 general formula V wherein D is functionalized with and hydroxyl group that can conveniently react under standard Mitsunobu conditions. The reaction is done in solvents such as THF or N-methyl-morpholine (NMM) at a temperature from -10 ºC to RT and completes in 1 to 24 hours. It occurs in the presence of diethyl azodicarboxylate (DEAD) or diisopropyl azodicarboxylate (DIAD) and an organic phosphine such as triphenylphosphine.
Alcohol of general formula VII is either commercially available or it can be prepared from compound of formula II by addition of a Grignard reagent of formula VI. The reaction is normally done in an aprotic solvent such as ether or THF at RT or lower temperature and completes over 0.5 to 12 hours. Alternatively it can be prepared by reduction of a compound of general formula II, wherein R2 is not hydrogen, with a reducing agent such as, but not limited to, NaBH4, leading in this case to a compound of formula VII wherein R1 is hydrogen. The reaction is performed in a solvent such as methanol, ethanol or THF and completes over a period of time ranging from 1 to 12 hours. A similar synthetic protocol can be used for the preparation of intermediate XII from compounds of general formula IV or XI.
It is clear to a person skilled in the art that the preparation of compound of general formula VII or XII can be accomplished via inverse Grignard reaction in which Grignard of formula G-MgBr react with a compound of formula R1C(O)R2 under the same reaction conditions described above.
If the reaction is performed on a compound of general formula XIII with a bi-functional Grignard reagent such as for example BrMg-R1-R2-MgBr, a compound of general formula XII, wherein R1 and R2 are connected to form a cycle, can be obtained. A similar synthetic protocol can be used for the preparation of intermediates of formula VII, wherein R1 and R2 are connected to form a cycle, from compounds of general formula VIII.
Compounds of general formula IV wherein E is -O- or -S-, can be 44 prepared from a compound of general formula II, following an approach similar to that described for the preparation of compounds of formula XII from VII. Alternatively the compounds of general formula IV can be obtained by alkylation of a compound of general formula II, with a compound of general formula III wherein LG is a suitable leaving group such as tosyl, mesyl or halogen. The reaction is normally done in polar solvents such as acetonitrile or DMF, occurs in a presence of a base such as for example alkaline carbonate, bicarbonates or organic bases and completes over a period of time varying from 1 to 24 hours.
Compounds of general formula XII, wherein D is alkenylene or alkynylene, n is 0 and E is absent, can be prepared by reacting a compound of formula XI under the same reaction condition described for the addition of a Grignard reagent of formula VI to a compound of formula II.
Preparation of compounds of formula XI can be achieved by reaction of a compound of general formula X, or the analogue wherein the bromine is substituted by iodine or triflate, with a compound of general formula IX, under transition metal catalyzed cross-coupling reaction conditions. A great number of protocols, reagents and catalysts can be conveniently used to achieve the desired conversion, as it is known to a person skilled in the art. It is clear that a compound of formula XI, wherein n is 0, E is absent and D is alkenylene or alkynylene, can be easily hydrogenated leading to the a compound of formula IV wherein D is the alkyl group derived from reduction of the unsaturated bond.
Alternatively, compounds of general formula I wherein M is -O-, can be prepared by treating a compound of general formula XXXIX with a compound of general formula XL.
In another embodiment of the present invention, compounds of general formula I can be prepared following a different synthetic approach in which a 45 compound of general formula XXVII is reacted with a compound of formula XXIX under the transition metal catalyzed cross-coupling reaction condition.
Alternatively it can be prepared by reaction of a compound of formula XXIV with a compound of formula XXX under the condition described above for the reaction of a compound of formula II with a compound of formula III.
Intermediates of formula XXVII and XXIV can be prepared by reaction of compound of formula XXII under reductive amination conditions, described above for the reaction of compound of formula XIX with XX, with compound of formula XXVI and XXIII respectively. Alternatively compounds of formula XXVII and XXIV can be prepared by alkylation of compound XXII with compound of formula XXVIII and XXV respectively under alkylation condition described above for the preparation of compound IV by reaction of compound II with compound III.
Compounds of general formula XXII can be obtained by opening the epoxide intermediates XXI with a benzyl amine optionally substituted on the phenyl ring. The reaction can be performed neat or in high boiling point solvent such as toluene, xylene, isopropanol or butanol and occurs at temperature ranging from 80 to 120 ºC. Classical thermal or microwaves heating is efficacious to drive the reaction to completion over 1 to 24 hours.
In an additional embodiment of the present invention, compounds of formula I, wherein R4 is J5 or another group featuring a quaternary ammonium salt, can be prepared reacting the corresponding tertiary amine precursor of formula I where R5 is J1-J4 with a compound of formula XXXI.
The reaction proceeds smoothly at RT or higher temperature in solvent such as DCM, acetonitrile, methanol or AcOEt over a period of time ranging from 1 to 24 hours.
In another embodiment of the present invention, compounds of general formula XXIV can be prepared by reacting an intermediate of general formula 46 XXXII with an amine of general formula XXXIII. This reaction is a common alkylation of amine in which the leaving group LG (normally chlorine, bromine or sulphate) is displaced by a nucleophile like the amine XXXIII wherein R3 is H or an alkyl group that can increase the selectivity and it can be removed after the reaction. Several methods to perform this reaction, that normally occurs in a polar solvent at a temperature higher than room temperature, are described in the literature.
It is apparent for those skilled in the art that compounds of general formula I wherein R4 is J1 or J2 contain three stereogenic centers, as indicated below with the symbol *. This means that the structure of formula I is characterized by eight different stereoisomers.
Each diastereoisomer can be obtained theoretically by chromatographic separation of the mixture obtained by reacting racemic mixtures of the required intermediates. It is clear that this approach it is not convenient and that it can be used only for the separation of mixtures containing few diastereoisomers.
In a more convenient approach, the synthesis of each single stereoisomer can be accomplished using, in the reactions described above, only enantiomerically pure intermediates.
The enantiomerically pure alcohol required for the preparation of compounds of general formula I wherein R4 is J1, J2 or J5 are commercially available.
The preparation of single enantiomerically pure compounds of general 47 formula XXXII wherein LG is bromine are described in WO2005/080324, US2005-2222128, WO2004/032921, US2005/215590 and WO2005/092861 (cited by WO2007/107228). This compound can be easily converted into the epoxide XXI by heating the precursor (wherein Z is oxygen) in a suitable solvent in the presence of a base that catalyzes the epoxide formation.
Enantiomerically pure compounds of general formula XXXV can be obtained by chiral chromatographic separation of the racemic mixture or starting from enantiomerically pure amine compounds of general formula XXXIV. As intermediate compounds of formula XXXIV contains a basic group, it is possible to obtain the two enantiomers by mean of crystallization of the diastereomeric salt, obtained by salification of the racemic mixture with an enantiomerically pure carboxylic acid. Widely used carboxylic acids used for this purpose are for example mandelic acid, tartaric acid and its derivatives. The base XXXIV is dissolved in a suitable polar solvent and then treated with of the carboxylic acid causing precipitation of one of the two diastereoisomeric salts. It could be required to repeat the procedure several times to obtain the desired level of optical purity.
Alternatively the amines of formula XXXIV can be obtained via enantioselective synthesis following for example the approach described in the literature (Tetrahedron: Asymmetry 13 (2002) 303–310) in which the aldehyde of formula II, wherein R2 is H, is treated first with a enantiomerically pure tert-butyl sulfiniimide and then with R2MgBr or R2Li (wherein R2 is not H), followed by hydrolysis of the intermediate leading to the formation of enantiomerically enriched compounds of formula XXXIV that can be used as such or further purified to increase the optical purity.
The available amine of formula XXXIV can be easily further derivatized under the reaction conditions described above. For example it can be treated with a protected aldehyde of formula III, under the conditions 48 described for the alkylation of compounds of formula II with compounds of formula III, leading to compound or general formula XXXVI. Deprotection of the amino group and reaction of compounds of formula XVII, lead to the preparation of a compound of general formula XVIII.
Alternatively, compound of general formula I can be prepared coupling a compound of general formula XXXIX with a compound of general formula XL leading to a compound of general formula I wherein C is –OCO-. This ester can be obtained under different reaction condition well known to those skilled in the art. The reaction requires the activation of the acid XXXIX with reactant such as DCC, EDC, HBTU HATU or it may be converted into the corresponding acyl chloride. The activated ester can smoothly react, in DCM, pyridine or other apolar solvents, with the alcohol of formula XL.
Compound of formula XXXIX can be prepared starting from XXXV via alkylation with compound of formula XXXVII, deprotection and reaction with compound of formula XVII. The reaction conditions for this conversion are described above and well described in the literature. Acid XXXIX can be easily reacted with a compound of formula XLI, as described above for the reaction with a compound of formula XL, leading to compound of formula XVIII.
A compound of general formula XL can be prepared by reaction of a compound of general formula XXXII with an amine of formula PG-NH-A1-BA2-OH, under the reaction conditions described for the reaction of compounds of general formula XXXII with compounds of general formula XXXIII.
For all the above, the synthesis of compounds of general formula I can be performed following several different approaches. In particular it must be noted that the sequence of reaction required, strongly depends on the nature of the linkers Y and Y1 and on the functional groups present on the linker. The example given above for the preparation of compounds of formula I wherein 49 C is –OCO- allows appreciating this aspect of the invention.
The LCMS methods A, B and C, used for the characterization of the compounds of the present invention, are described in the following: Method A (IS 10cm_ESCI_Formic_MeCN) HPLC Setup Solvents: Acetonitrile (Far UV grade) with 0.1% (V/V) formic acid Water (High purity via PureLab Option unit) with 0.1% formic acid Column: Phenomenex Luna 5 µ C18 (2), 100 x 4.6mm. (Plus guard cartridge) Flow Rate: 2ml/min Gradient: A: Water / formic B: MeCN/formic Time A% B% 0.00 95 5 3.50 5 95 .50 5 95 .60 95 5 6.50 95 5 Typical Injections 2-7ul UV detection via HP or Waters DAD Start Range (nm) 210 End Range (nm) 400 Range interval (nm) 4.0 Optional ELS detection using Polymer Labs ELS-1000.
MS detection: Micromass ZQ, single quadrapole LC-MS instrument.
Scan range for MS Data (m/z) Start (m/z) 100 End (m/z) 650 or 1000 when required With +ve / -ve switching Ionisation is either electrospray (ESI) or atmospheric-pressure chemical 50 ionization (APCI) dependent on compound types.
Method B (IS 15cm_Formic_ASCENTIS_HPLC_CH3CN) HPLC Setup Solvents: Acetonitrile (Far UV grade) with 0.1% (V/V) formic acid Water (High purity via PureLab Ultra unit) with 0.1% formic acid Column: Supelco, Ascentis® Express C18 or Hichrom Halo C18, 2.7 µm C18, 150 x 4.6 mm.
Flow Rate: 1 ml/min Gradient: A: Water / formic B: MeCN/formic Time A% B% 0.00 96 4 3.00 96 4 9.00 0 100 13.6 0 100 13.7 96 4 96 4 Typical Injections 0.2-10 ul Maximum pressure setting 400 bar.
Instrument: Agilent 1100, Binary Pump, Agilent Sampler and Agilent DAD detector Diode array detection: (300nm, Band Width 200nm; Ref. 450nm, Band Width 100 nm) Method C (IS 10cm_ESCI_Formic_MeCN) HPLC Setup Solvents: Acetonitrile (Far UV grade) with 0.1% (V/V) formic acid Water (High purity via PureLab Ultra unit) with 0.1% formic acid Column: Hichrom ACE 3 C18-AR mixed mode column 100x4.6mm Flow Rate: ml/min 51 Gradient: A: Water / formic B: MeCN/formic Time A% B% 0.00 98 2 3.00 98 2 12.00 0 100 .4 0 100 .5 98 2 17 98 2 Typical Injections 0.2-10ul Maximum pressure setting 400 bar.
Instrument: Agilent 1100, Binary Pump, Agilent Sampler and Agilent DAD detector Diode array detection: (300nm, Band Width 200nm; Ref. 450nm, Band Width The invention also provides pharmaceutical compositions of compounds of formula I in admixture with one or more pharmaceutically acceptable carriers, for example those described in Remington’s Pharmaceutical Sciences Handbook, XVII Ed., Mack Pub., N.Y., U.S.A.
Administration of the compounds of the present invention may be accomplished according to patient needs, for example, orally, nasally, parenterally (subcutaneously, intravenously, intramuscularly, intrasternally and by infusion), by inhalation, rectally, vaginally, topically, locally, transdermally, and by ocular administration.
Various solid oral dosage forms can be used for administering compounds of the invention including such solid forms as tablets, gelcaps, capsules, caplets, granules, lozenges and bulk powders. The compounds of the present invention can be administered alone or combined with various pharmaceutically acceptable carriers, diluents (such as sucrose, mannitol, 52 lactose, starches) and known excipients, including suspending agents, solubilizers, buffering agents, binders, disintegrants, preservatives, colorants, flavorants, lubricants and the like. Time release capsules, tablets and gels are also advantageous in administering the compounds of the present invention.
Various liquid oral dosage forms can also be used for administering compounds of the invention, including aqueous and non-aqueous solutions, emulsions, suspensions, syrups, and elixirs. Such dosage forms can also contain suitable known inert diluents such as water and suitable known excipients such as preservatives, wetting agents, sweeteners, flavorants, as well as agents for emulsifying and/or suspending the compounds of the invention. The compounds of the present invention may be injected, for example, intravenously, in the form of an isotonic sterile solution. Other preparations are also possible.
Suppositories for rectal administration of the compounds of the invention can be prepared by mixing the compound with a suitable excipient such as cocoa butter, salicylates and polyethylene glycols.
Formulations for vaginal administration can be in the form of cream, gel, paste, foam, or spray formula containing, in addition to the active ingredient, such as suitable carriers, are also known.
For topical administration the pharmaceutical composition can be in the form of creams, ointments, liniments, lotions, emulsions, suspensions, gels, solutions, pastes, powders, sprays, and drops suitable for administration to the skin, eye, ear or nose. Topical administration may also involve transdermal administration via means such as transdermal patches.
For the treatment of the diseases of the respiratory tract, the compounds according to the invention are preferably administered by inhalation.
Inhalable preparations include inhalable powders, propellant-containing metering aerosols or propellant-free inhalable formulations. 53 For administration as a dry powder, single- or multi-dose inhalers known from the prior art may be utilized. In that case the powder may be filled in gelatine, plastic or other capsules, cartridges or blister packs or in a reservoir.
A diluent or carrier, generally non-toxic and chemically inert to the compounds of the invention, e.g. lactose or any other additive suitable for improving the respirable fraction may be added to the powdered compounds of the invention.
Inhalation aerosols containing propellant gas such as hydrofluoroalkanes may contain the compounds of the invention either in solution or in dispersed form. The propellant-driven formulations may also contain other ingredients such as co-solvents, stabilizers and optionally other excipients.
The propellant-free inhalable formulations comprising the compounds of the invention may be in form of solutions or suspensions in an aqueous, alcoholic or hydroalcoholic medium and they may be delivered by jet or ultrasonic nebulizers known from the prior art or by soft-mist nebulizers such as Respimat .
The compounds of the invention may be administered as the sole active agent or in combination with other pharmaceutical active ingredients including those currently used in the treatment of respiratory disorders, e.g. corticosteroids, P38 MAP kinase inhibitors, IKK2, HNE inhibitors, PDE4 inhibitors, leukotriene modulators, NSAIDs and mucus regulators.
The dosages of the compounds of the invention depend upon a variety of factors including the particular disease to be treated, the severity of the symptoms, the route of administration, the frequency of the dosage interval, the particular compound utilized, the efficacy, toxicology profile, and pharmacokinetic profile of the compound. 54 Advantageously, the compounds of formula I can be administered for example, at a dosage comprised between 0.001 and 1000 mg/day, preferably between 0.1 and 500 mg/day.
When the compounds of formula I are administered by inhalation route, they are preferably given at a dosage comprised between 0.001 and 500 mg/day, preferably between 0.1 and 200 mg/day.
The compounds of formula I may be administered for the prevention and/or treatment of broncho-obstructive or inflammatory diseases, such as asthma, chronic bronchitis, chronic obstructive pulmonary disease (COPD), bronchial hyperreactivity, cough, emphysema or rhinitis; urological disorders such as urinary incontinence, pollakiuria, cystospasm, chronic cystitis and overactive bladder (OAB); gastrointestinal disorders such as bowel syndrome, spastic colitis, diverticulitis, peptic ulceration, gastrointestinal motility or gastric acid secretion; dry mouth; mydriasis, tachycardia; ophthalmic interventions cardiovascular disorders such as vagally induced sinus bradycardia.
The present invention will now be further described by way of the following examples.
The intermediate compounds for the synthesis of final compounds of general formula (I) were obtained through the preparations herebelow described.
Preparation of 9-Bromononanal Br H O Pyridinium chlorochromate (38.7 g, 180 mmol) and silica 60A (39 g, particle size 35-70 micron) suspended in DCM (250 mL) were stirred at RT for 45 minutes. 9-Bromononanol (26.7 g, 120 mmol) was added, in one 55 portion, and the suspension was stirred at RT for 18 hours. The reaction mixture was filtered through a celite plug and the resulting filtrate concentrated under vacuum affording the title compound (28.0 g, >100%).
The material was used without further purification in the next step.
¹H NMR (400 MHz, CDCl3): δ 9.77 (s, 1 H), 3.41 (t, 2 H), 2.43 (t, 2 H), 1.90-1.80 (m, 2 H), 1.63 (s, 2 H), 1.43 (s, 2 H), 1.32 (s, 6 H).
Preparation of 2-(8-Bromooctyl)-1,3-dioxolane Br O O 9-Bromononanal (28.0 g, assumed 120 mmol), ethylene glycol (33.6 mL, 600 mmol) and para-toluenesulphonic acid (2.7 g, 13 mmol) in toluene (210 mL) were heated at reflux for 20 hours. The reaction was cooled to RT and quenched with saturated aqueous sodium bicarbonate solution (300 mL). The resulting mixture was extracted with diethyl ether (2 x 500 mL). The combined organic extracts were washed with saturated aqueous sodium bicarbonate solution (300 mL), water (300 mL), brine (100 mL), dried (magnesium sulfate), filtered and evaporated under reduced pressure to afford the title compound (25.2 g, 79%).
¹H NMR (400 MHz, CDCl3): δ 4.84 (t, J = 4.8 Hz, 1 H), 3.95-3.78 (m, 4 H), 3.43-3.37 (m, 2 H), 1.90-1.79 (m, 2 H), 1.69-1.54 (m, 2 H), 1.42 (s, 3 H), 1.32 (s, 7 H).
Alternatively 9-Bromononanal could be prepared as follows: To a cooled (-78°C) solution of oxalyl chloride (11.66 g, 92 mmol) in DCM (250 mL), a solution of dimethylsulfoxide (DMSO) (13.0 mL, 183 mmol) in DCM (50 mL) was added over 15 minutes. After a further 5 minutes a solution of 9-bromononanol (10.25 g, 45.9 mmol) in DCM (50 mL) was added dropwise over 15 minutes. The resulting reaction mixture was 56 stirred at this temperature for 45 minutes. Triethylamine (32 mL, 230 mmol) was added and the reaction mixture stirred at this temperature for 10 minutes.
The coolant was removed and allowed to warm to RT. The reaction mixture was stirred at RT for 40 minutes and then diluted with water. The organic phase was removed and washed with 10% aqueous potassium hydrogen sulfate and dried (magnesium sulfate). The suspension was filtered and the filtrate evaporated under reduced pressure to afford the title compound.
All other 1,3-dioxalanes (i.e. 2-(7-bromoheptyl)-1,3-dioxolane; 2-(6-bromohexyl)-1,3-dioxolane; 2-(5-bromopentyl)-1,3-dioxolane and 2-(4-bromobutyl)-1,3-dioxolane) were prepared by the same method.
Preparation of 8-(Benzyloxy)(2-bromoacetyl)quinolin-2(1H)-one N H O O O Br To a suspension of 5-acetyl(benzyloxy)quinolin-2(1H)-one (19.4 g, 66.4 mmol) in anhydrous THF (240 mL) and anhydrous methanol (165 mL) was added a solution of tetra-n-butylammonium tribromide (54.5 g, 113.0 mmol) in anhydrous THF (130 mL) dropwise over 1.5 hours. The resulting solution was stirred at RT overnight before concentrating under reduced pressure without heating. The residue was re-dissolved in methanol (200 mL).
Saturated aqueous ammonium chloride solution (390 mL) was added with icecooling. The resulting suspension was filtered and the solid washed with water and air-dried under vacuum. The solid was suspended in DCM and methanol (1:1 v/v, 100 mL) for 90 minutes. The solid was collected by filtration, washed with DCM and air-dried to afford the title compound (18.0 g, 73%). 57 ¹H NMR (400 MHz, DMSO-d6): δ 11.07 (s, 1 H), 8.51 (d, J = 10.0 Hz, 1 H), 7.94-7.83 (m, 1 H), 7.60 (d, J = 7.5 Hz, 2 H), 7.44-7.27 (m, 4 H), 6.79-6.65 (m, 1 H), 5.53-5.39 (s, 2 H); 4.93 (s, 2 H) Preparation of (R)(Benzyloxy)(2-bromohydroxyethyl)- quinolin-2(1H)-one N H O O HO Br 8-(Benzyloxy)(2-bromoacetyl)quinolin-2(1H)-one (26.0 g, 69.9 mmol) and (R)-3,3-diphenylmethyltetrahydro-3H-pyrrolo[1,2- c][1,3,2]oxazaborole (21.3 g, 76.8 mmol) were azeotroped with toluene (× 3) then suspended in anhydrous THF (400 mL) under an atmosphere of nitrogen.
The suspension was cooled to -20°C (external temperature) and borane dimethyl sulfide complex solution (45.4 mL, 90.8 mmol, 2.0 M solution in THF) was added by syringe pump over 3 hours. After complete addition the reaction mixture was stirred for one hour before quenching with methanol (25 mL). The reaction was warmed to RT over 20 minutes. The mixture was concentrated under reduced pressure and the residue was suspended in aqueous hydrochloric acid (500 mL, 1 M solution) and stirred at RT for 18 hours. After this time the solid was collected by filtration and washed with water (3 × 100 mL). The solid was partially dissolved in ethyl acetate and heated at reflux for 2 hours. The remaining solid was removed by hot filtration and the filtrate was evaporated to afford the title compound. The solid collected from the hot ethyl acetate was again partially dissolved in ethyl acetate and heated at reflux for 2 hours then filtered to give filtrate containing pure product. This 58 process was repeated four more times. The combined solid was recrystallised from ethyl acetate and petroleum ether to afford the title compound (20.0 g, 76%).
¹H NMR (400 MHz, DMSO-d6): δ 10.68 (s, 1 H); 8.19 (d, J = 9.9 Hz, 1 H); 7.58 (d, J = 7.5 Hz, 2 H); 7.41-7.36 (m, 2 H); 7.34-7.29 (m, 1 H); 7.23-7.19 (m, 2 H); 6.57 (d, J = 9.8 Hz, 1 H); 5.94 (d, J = 4.7 Hz, 1 H); 5.31 (s, 2 H); 5.25-5.19 (m, 1 H); 3.71-3.58 (m, 2 H).
Preparation of (R)(Benzyloxy)(2-bromo(tertbutyldimethylsilyloxy)ethyl)quinolin-2(1H)-one N H O O TBDMSO Br 2,6-Lutidine (6.9 mL, 59.5 mmol) was added to a solution of (R)(benzyloxy)(2-bromohydroxyethyl)quinolin-2(1H)-one (10.1 g, 27.0 mmol) in DCM (100 mL) at 0°C. The reaction mixture was stirred for 5 minutes then tert-butyldimethylsilyl trifluoromethanesulfonate (13.0 mL, 56.8 mmol) was added dropwise over 15 minutes. The mixture was stirred at 0°C for 30 minutes, followed by RT overnight. After this time the reaction was quenched with saturated aqueous sodium bicarbonate solution and extracted with DCM (x 3). The combined organic extracts were dried (magnesium sulfate), filtered and concentrated under reduced pressure.
Iso-hexane (500 mL) was added to the crude material and the resulting solid collected by filtration. The solid was recrystallised from ethyl acetate and petroleum ether (40 : 60) to afford the title compound (11.3 g, 85%).
¹H NMR (400 MHz, CDCl3): δ 9.19 (s, 1 H), 8.23 (dd, J = 9.9, 4.4 Hz, 1 H), 7.43 (d, J = 4.6 Hz, 5 H), 7.17 (dd, J = 8.3, 4.5 Hz, 1 H), 7.03 (dd, J = 8.2, 59 4.4 Hz, 1 H), 6.71 (dd, J = 9.9, 3.7 Hz, 1 H), 5.18 (d, J = 4.5 Hz, 3 H), 3.63-3.56 (m, 1 H), 3.49 (dd, J = 10.4, 4.8 Hz, 1 H), 0.88 (t, J = 4.4 Hz, 9 H), 0.14 (d, J = 4.4 Hz, 3 H), -0.11 (d, J = 4.4 Hz, 3 H).
Preparation of (R)(2-Azido(tert-butyldimethylsilyloxy)ethyl)- 8-(benzyloxy)quinolin-2(1H)-one N H O O TBDMSO N3 (R)(Benzyloxy)(2-bromo(tert-butyldimethylsilyloxy)ethyl)- quinolin-2(1H)-one (5.0 g, 10.2 mmol) was dissolved in dimethyl formamide (90 mL) and water (10 mL). Sodium iodide (1.7 g, 11.3 mmol) and sodium azide (0.7 g, 11.3 mmol) were added sequentially. The reaction mixture was stirred at RT until all the solid was in solution. The solution was heated at 80°C for 40 hours then cooled to RT and diluted with water (300 mL). The aqueous layer was extracted with DCM and the combined organic extracts were dried (magnesium sulfate), filtered and concentrated under reduced pressure. The crude residue was recrystallised from ethyl acetate and iso-hexane to afford the desired compound (3.6 g, 78%). Used without further purification in the next step.
¹H NMR (400 MHz, CDCl3): δ 9.19 (s, 1 H), 8.18 (d, J = 9.9 Hz, 1 H), 7.45-7.36 (m, 4 H), 7.20 (d, J = 8.3 Hz, 1 H), 7.04 (d, J = 8.3 Hz, 1 H), 6.70 (dd, J = 9.9, 2.2 Hz, 1 H), 5.19-5.13 (m, 3 H), 3.48 (dd, J = 12.7, 8.1 Hz, 1 H), 3.26 (dd, J = 12.7, 3.8 Hz, 1 H), 0.89 (s, 9 H), 0.14 (s, 3 H), -0.11 (s, 3 H). 60 Preparation of (R)(2-Amino(tert-butyldimethylsilyloxy)ethyl)- 8-hydroxyquinolin-2(1H)-one formate N H OH O TBDMSO NH2.HCO2H Palladium on activated carbon (0.4 g, 10% w/w) was added to a suspension of (R)(2-azido(tert-butyldimethylsilyloxy)ethyl) (benzyloxy)quinolin-2(1H)-one (2.05 g, 4.60 mmol) and ammonium formate (2.87 g, 63 mmol) in methanol (50 mL). The reaction mixture was heated at 80°C for 1 hour. If after this time the reaction had not reached completion; the reaction mixture was filtered through celite, washing with methanol. The reaction mixture was concentrated to approximately 50 mL then ammonium formate (2.87 g, 63.0 mmol) and Palladium on activated carbon (0.40 g, 10% w/w) were added. The reaction mixture was heated at 80°C for 20 minutes, and then filtered through celite, washing with water. The reaction mixture was concentrated under reduced pressure. The resulting solid was washed with water, triturated with ethyl acetate and collected by filtration to afford the title compound (1.32 g, 86%).
¹H NMR (400 MHz, DMSO-d6): δ 8.34 (s, 1 H), 8.31-8.22 (m, 1 H), 7.03 (d, J = 8.1 Hz, 1 H), 6.98-6.90 (m, 1 H), 6.53 (d, J = 9.9 Hz, 1 H), 5.13 (t, J = 6.0 Hz, 1 H), 3.18 (s, 1 H), 2.84-2.73 (m, 2 H), 0.83 (s, 9 H), 0.06 (s, 3 H), -0.17 (s, 3 H).
Preparation of (R)(2-Amino(tert-butyldimethylsilyloxy)ethyl)- 8-hydroxyquinolin-2(1H)-one N H OH O TBDMSO NH2 61 To an ice-cooled suspension of (R)(2-azido(tertbutyldimethylsilyloxy)ethyl)(benzyloxy)quinolin-2(1H)-one (5.77 g, 12.8 mmol) and palladium on activated charcoal (5.8 g, 10% w/w wet) in ethanol (50 mL), 1,4-cyclohexadiene (12.0 mL, 126 mmol) was added dropwise. After stirring at this temperature for 30 minutes the coolant was removed and replaced with a water bath at 30 ºC. The reaction was stirred at this temperature for 1 hour. The suspension was filtered and the filter cake washed with further ethanol. The filtrate was evaporated under reduced pressure to dryness. The resulting solid was suspended in acetonitrile and stirred for 1 hour. The suspension was filtered and the resulting solid air-dried under vacuum to afford the title compound (2.90 g, 87%).
¹H NMR (400 MHz, DMSO-d6): δ 8.43 (d, J = 10 Hz, 1 H), 7.18 (d, J = 8.0 Hz, 1 H), 7.08 (d, J = 8.4 Hz, 1 H), 6.68 (d, J = 10 Hz, 1 H), 5.14 (m, 1 H), 2.84-2.82 (m, 2 H), 0.96 (s, 9 H), 0.19 (s, 3 H), 0.00 (s, 3 H).
Preparation of (R)(2-Aminohydroxyethyl)hydroxyquinolin2(1H)-one hydrochloride N H OH O HO NH2.HCl (R)(2-Amino(tert-butyldimethylsilyloxy)ethyl) hydroxyquinolin-2(1H)-one formate (0.23 g, 0.61 mmol) was dissolved in hydrochloric acid (5 mL, 4 M solution in dioxane) and methanol (5 mL). The reaction mixture was stirred at RT for 16 hours before concentrating in vacuo.
The resulting residue was washed with ethyl acetate and dried in a vacuum oven for 18 hours to afford the title compound (0.15 g, 99%).
¹H NMR (400 MHz, MeOD): δ 7.71 (d, J = 9.8 Hz, 1 H), 6.57 (d, J = 8.2 Hz, 1 H), 6.31 (d, J = 8.2 Hz, 1 H), 6.02 (dd, J = 9.8, 6.5 Hz, 1 H), 4.58 62 (dd, J = 9.6, 3.5 Hz, 1 H), 2.47-2.31 (m, 2 H).
Preparation of (R)-Quinuclidinyl carbonochloridate hydrochloride O O N Cl To a stirred solution of (R)quinuclidinol (2.5 g, 19.66 mmol) in acetonitrile (200 mL), trichloromethyl chloroformate (3.06 mL, 25.57 mmol) was added dropwise at 0 ºC and stirred for 1 hour. The reaction mixture was stirred at RT for 16 hours before concentrating in vacuo to afford the title compound (4.39 g, 98%).
¹H NMR (400 MHz, DMSO-d6): δ 10.29 (s, 1 H), 4.05-3.95 (m, 1 H), 3.43 (t, J = 10.78 Hz, 1 H), 3.12 (m, 3 H), 3.10-2.95 (m, 1 H), 2.79 (d, J = 13.27 Hz, 1 H), 2.12-2.02 (m, 1 H), 1.98 (m, J = 3.36 Hz, 1 H), 1.89-1.78 (m, 1 H), 1.75-1.59 (m, 2 H).
Preparation of 1-Benzylpiperidinyl carbonochloridate hydrochloride O O Cl N Title compound prepared as described above for (R)-quinuclidinyl carbonochloridate to afford the title compound (0.6 g, 99%) which was used without further purification.
¹H NMR (400 MHz, DMSO-d6): δ 10.33 (s, 1 H), 7.60 (d, J = 13.85 Hz, 2 H), 7.47-7.44 (m, 3 H), 4.27 (dd, J = 16.57, 5.30 Hz, 2 H), 3.66-3.56 (m, 1 H), 3.28 (d, J = 12.34 Hz, 1 H), 3.12 (s, 2 H), 2.91 (q, J = 11.35 Hz, 1 H), 1.94 (d, J = 13.65 Hz, 2 H), 1.77-1.62 (m, 2 H).
Preparation of 1-Methylpiperidinyl carbonochloridate hydrochloride O O Cl N Title compound prepared as described above for (R)-quinuclidinyl 63 carbonochloridate to afford the title compound (0.42 g, 90%) which was used without further purification.
¹H NMR (400 MHz, DMSO-d6): δ 10.63 (s, 1 H); 3.93-3.89 (m, 1 H), 3.36-3.27 (m, 1 H), 3.19-3.04 (m, 2 H), 2.97-2.86 (m, 1 H), 2.70-2.63 (m, 3 H), 2.00-1.85 (m, 2 H), 1.76-1.61 (m, 2 H).
Preparation of 8-Benzylazabicyclo[3.2.1]octanyl carbonochloridate hydrochloride N O O Cl H Title compound prepared as described above for (R)-quinuclidinyl carbonochloridate to afford the title compound (0.31 g, 84%) which was used without further purification.
¹H NMR (400 MHz, DMSO-d6): δ 7.68 (s, 2 H), 7.47 (s, 3 H), 4.13 (d, J = 6.31 Hz, 1 H), 3.99-3.90 (m, 2 H), 3.72 (s, 2 H), 2.27 (s, 2 H), 1.88 (t, J = 11.52 Hz, 6 H). 64 N H N H O OH HO K2CO3 , DMF 80 °C i) Et3N, MeOH ii) NaBH(OAc)3 , HOAc, RT HN NH2.HCl O HO OH 8 O O Br 8 Toluene, 45 °C - RT N3 O O O 8 NH2 O O O 8 HN O O O 8 O O N O O N Cl pyridine aq. HCl THF HN O O 8 O O N H O HN O O N LiAlH4 THF -78 °C- 0 °C DPPA, DBU O OH O O O O 8 OH O O O 8 NaBH4 EtOH Example 1 (R)-Quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(phenyl)- methylcarbamate (compound 1) N H HO N H O OH O H N O O N Step 1; (3-(8-(1,3-Dioxolanyl)octyloxy)phenyl)(phenyl)methanone O O O O 65 2-(8-Bromooctyl)-1,3-dioxolane (3.89 g, 14.69 mmol) was added to a mixture of 3-hydroxybenzophenone (3 g, 15.13 mmol) and potassium carbonate (4.17 g, 30.21 mmol) in dimethyl formamide (50 mL). The reaction mixture was stirred at 80 ºC for 16 hours. The reaction mixture was diluted with water and extracted with ethyl acetate (x 3). The combined organic extracts were washed with saturated aqueous sodium bicarbonate solution, saturated aqueous ammonium chloride solution and dried (sodium sulfate), filtered and concentrated under reduced pressure. The crude material was purified by silica gel column chromatography eluting with 0-100% ethyl acetate in iso-hexane to afford the title compound (4.73 g, 84%).
¹H NMR (400 MHz, DMSO-d6): δ 7.74 (d, J = 7.53 Hz, 2 H), 7.69-7.66 (m, 1 H), 7.60-7.53 (m, 2 H), 7.46-7.43 (m, 1 H), 7.28-7.20 (m, 3 H), 4.77- 4.71 (m, 1 H), 4.04-3.97 (m, 2 H), 3.90-3.80 (m, 2 H), 3.79-3.69 (m, 2 H), 1.77-1.66 (m, 2 H), 1.57-1.50 (m, 2 H), 1.54-1.15 (m, 10 H).
Step 2; (3-(8-(1,3-Dioxolanyl)octyloxy)phenyl)(phenyl)methanol OH O O O To a solution of (3-(8-(1,3-dioxolanyl)octyloxy)phenyl)(phenyl)- methanone (4.73 g, 12.35 mmol) in ethanol (100 mL) at 0 ºC sodium borohydride (1.88 g, 49.42 mmol) was added portion wise. The coolant was removed and the reaction mixture was allowed to warm to RT and stirred for 1 hour. The reaction mixture was quenched with water (30 mL) at 0 ºC and then concentrated under reduced pressure. The crude material was dissolved in DCM and washed with saturated aqueous ammonium chloride, dried (sodium sulfate), filtered and concentrated under reduced pressure to afford the title compound (4.33 g, 91%). 66 ¹H NMR (400 MHz, DMSO-d6): δ 7.37 (d, J = 1.27 Hz, 2 H), 7.32-7.28 (m, 2 H), 7.23-7.16 (m, 2 H), 6.96-6.90 (m, 2 H), 6.75 (dd, J = 8.11, 2.58 Hz, 1 H), 5.85 (d, J = 4.08 Hz, 1 H), 5.65 (d, J = 4.05 Hz, 1 H), 4.79-4.73 (m, 1 H), 3.93-3.80 (m, 4 H), 3.79-3.70 (m, 2 H), 1.73-1.62 (m, 2 H), 1.59-1.51 (m, 2 H), 1.73-0.95 (m, 10 H).
Step 3; 2-(8-(3-(Azido(phenyl)methyl)phenoxy)octyl)-1,3-dioxolane N3 O O O To a stirred solution of (3-(8-(1,3-dioxolanyl)octyloxy)phenyl)- (phenyl)methanol (1.63 g, 4.24 mmol) in toluene (10 mL) under an atmosphere of nitrogen diphenylphosphoryl azide (1.10 mL, 5.10 mmol) and DBU (0.77 mL, 5.11 mmol) was added. The reaction mixture was stirred at 45°C for 3 hours and then at RT for 16 hours. The reaction mixture was concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 0-100% ethyl acetate in iso-hexane to afford impure title compound (1.11 g, 64%). This material was used directly in the next step.
Step 4; (3-(8-(1,3-Dioxolanyl)octyloxy)phenyl)(phenyl)methanamine NH2 O O O To a stirred solution of 2-(8-(3-(azido(phenyl)methyl)phenoxy)octyl)- 1,3-dioxolane (1.11 g, 2.71 mmol) in THF (15 mL) at -78°C under an atmosphere of nitrogen a solution of lithium aluminium hydride (2.0M in 67 THF, 2.8 mL, 5.60 mmol) was added drop wise. After stirring the reaction at -78°C for 1 hour the reaction mixture was warmed up to 0°C for 1 hour. The reaction mixture was quenched with water (304 mL), 2M sodium hydroxide (304 mL) and water (304 mL x 3). Anhydrous magnesium sulphate and ethyl acetate were added and the reaction mixture filtered and concentrated under reduced pressure. The crude material was purified by column chromatography eluting with 100% iso-hexane to 100% DCM to 25:1 DCM:methanol (0.63 g, 39% based on (3-(8-(1,3-dioxolanyl)octyloxy)phenyl)(phenyl)methanol).
¹H NMR (400 MHz, CDCl3): δ 7.39-7.18 (m, 6 H), 7.00-6.91 (m, 2 H), 6.76-6.73 (m, 1H), 5.17 (s, 1 H), 4.84 (t, J = 4.8 Hz, 1H), 4.00-3.83 (m, 6 H), 1.79-1.53 (m, 8 H), 1.43-1.33 (m, 8 H).
Step 5; (R)-Quinuclidinyl (3-(8-(1,3-dioxolanyl)octyloxy)- phenyl)(phenyl)methylcarbamate HN O O O O O N To a stirred solution of (3-(8-(1,3-dioxolanyl)octyloxy)phenyl)- (phenyl)-methanamine (0.62 g, 1.62 mmol) in pyridine (10 mL) at 0°C, (R)- quinuclidinyl carbonochloridate (0.48 g, 2.1 mmol) was added. The reaction was stirred at 0°C for 1 hour and then allowed to warm to RT for 16 hours. Water was added to the reaction mixture and extracted with ethyl acetate (x 3). The combined extracts were washed with brine, dried (sodium sulfate), filtered and concentrated under reduced pressure. The crude material was purified by chromatography on a KP-NH Biotage cartridge eluting with 0-20% methanol in ethyl acetate to afford the title compound (0.67 g, 78%).
H NMR (400 MHz, CDCl3): δ 7.41-7.18 (m, 6 H), 6.87-6.74 (m, 3 H), 68 .96-5.82 (br m, 1 H), 5.32 (br s, 1 H), 4.86-4.82 (m, 1 H), 4.76-4.69 (m, 1 H), 4.01-3.81 (m, 6 H), 3.20 (br s, 1 H), 2.96-2.60 (m, 5 H), 2.00 (br s, 1 H), 1.79-1.19 (m, 17 H).
Step 6; (R)-Quinuclidinyl (3-(9-oxononyloxy)phenyl)(phenyl)- methylcarbamate HN O O O O N H To a stirred solution of (R)-quinuclidinyl (3-(8-(1,3-dioxolan yl)octyloxy)phenyl)(phenyl)methylcarbamate (0.66 g, 1.23 mmol) in THF (10 mL) 2M hydrochloric acid was added (20 mL). The reaction mixture was stirred at RT for 3 hours. To the reaction mixture was added 10% aqueous potassium carbonate and the mixture extracted with DCM (x 3). The combined organic extracts were washed poured through a hydrophobic cartridge and concentrated under reduced pressure to afford the title compound (0.64 g, quantitative yield).
The material was used directly in the next step with no further purification.
Step 7; (R)-Quinuclidinyl (3-(9-((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethylamino)nonyloxy)phenyl)- (phenyl)methylcarbamate To a suspension of (R)(2-aminohydroxyethyl)hydroxyquinolin20 2(1H)-one hydrochloride (0.17 g, 0.66 mmol) in methanol (2.5 mL), triethylamine (0.18 mL, 1.32 mmol) was added and the reaction mixture stirred for 10 minutes at RT. The reaction mixture was then added with a solution of (R)-quinuclidinyl (3-(9-oxononyloxy)phenyl)(phenyl)- methylcarbamate (0.33 g, 0.66 mmol) in methanol (2.5 mL) and the reaction mixture was stirred at RT for 1 hour. The reaction mixture was added with 69 sodium triacetoxyborohydride (0.26 g, 1.23 mmol) followed by acetic acid (0.15 mL, 2.64 mmol). The reaction mixture was stirred at RT for 16 hours.
Water was added and the reaction mixture concentrated under reduced pressure. The crude material was purified by reverse phase preparative HPLC to afford the title compound (0.041 g, 9%).
The following compounds were prepared using the procedure described for the preparation of compound 1: Compound R4 m 2 N 7 3 N 6 4 N N 4 6 N 8 7 N 8 8 N 8 Example 9 (R)-Quinuclidinyl (4-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(phenyl)- 70 methylcarbamate (compound 9) N H HO N H O OH O NH O O N The title compound was prepared as in Example 1 with 4-hydroxybenzophenone replacing 3-hydroxybenzophenone in Step 1. The additional steps required to make the target compound are described in the preparation of Example 1.
N H N H O OH HO K2CO3 , DMF 80 °C i) Et3N, MeOH ii) NaBH(OAc)3 , HOAc, RT HN NH2.HCl O HO OH 8 H O OH O O Br 8 H O O O O 8 MgBr THF -78 °C- RT OH Toluene, 45 °C - RT O O O 8 N3 O O O 8 NH2 O O O 8 HN O O O 8 O O N O O N Cl pyridine aq. HCl THF HN O O 8 O O N H O HN O O N LiAlH4 THF -78 °C- 0 °C DPPA, DBU Example 10 (R)-Quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- 71 dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(thiophen yl)methylcarbamate (compound 10) N H HO N H O OH O H N O O S N Step 1; 3-(8-(1,3-Dioxolanyl)octyloxy)benzaldehyde O H O O O To a stirred solution of 2-(8-bromooctyl)-1,3-dioxolane (5 g, 18.85 mmol) in dimethyl formamide (100 mL) was added 3-hydroxybenzaldehyde (2.37 g, 19.42 mmol) and potassium carbonate (5.37 g, 38.83 mmol). The reaction mixture was stirred at 80°C for 16 hours.
The reaction mixture was diluted with water and extracted with ethyl acetate (x 3). The combined organic extracts were washed with saturated aqueous sodium hydrogen carbonate solution and brine, dried (sodium sulfate), filtered and concentrated under reduced pressure. The crude material was purified by silica gel column chromatography eluting with 0-100% ethyl acetate in iso-hexane to afford the title compound (4.66 g, 78%).
¹H NMR (400 MHz, CDCl3): δ 9.97 (s, 1 H); 7.46-7.40 (m, 2 H); 7.38 (d, J = 2.59 Hz, 1 H); 7.20-7.14 (m, 1 H); 4.84 (t, J = 4.82 Hz, 1 H); 4.05-3.93 (m, 4 H); 3.89-3.81 (m, 2 H); 1.85-1.74 (m, 2 H); 1.55-1.27 (m, 12 H).
Step 2; (3-(8-(1,3-Dioxolanyl)octyloxy)phenyl)(thiophen yl)methanol OH O O O S 72 To a stirred solution of 3-(8-(1,3-dioxolanyl)octyloxy)benzaldehyde (1.0 g, 3.25 mmol) in THF (30 mL) at -78°C under an atmosphere of nitrogen, a solution of 2-thienylmagnesium bromide (1M in THF, 4.23 mL, 4.23 mmol) was added over 10 minutes. After stirring at -78°C for 1 hour the reaction was allowed to warm to RT and stirred for 16 hours. The reaction was quenched with saturated aqueous ammonium chloride solution and extracted with ethyl acetate (x 3). The combined organic extracts were washed with brine, dried (magnesium sulfate), filtered and concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 0-50% ethyl acetate in iso-hexane to afford the title compound (1.12 g, 87%).
¹H NMR (400 MHz, CDCl3): δ 7.29-7.22 (m, 2 H), 7.05-6.95 (m, 2 H), 6.96-6.92 (m, 1 H), 6.89 (dt, J = 3.58, 1.09 Hz, 1 H), 6.85-6.81 (m, 1 H), 6.02 (s, 1 H), 4.83 (t, J = 4.83 Hz, 1 H), 4.06-3.89 (m, 4 H), 3.89-3.81 (m, 2 H), 2.47 (s, 1 H), 1.81-1.69 (m, 2 H), 1.70-1.58 (m, 2 H), 1.49-1.21 (m, 10 H).
The title compound was prepared as described in Example 1 with (3-(8-(1,3-dioxolanyl)octyloxy)phenyl)(thiophenyl)methanol replacing (3-(8-(1,3-dioxolanyl)octyloxy)phenyl)(phenyl)methanol in Step 3. The additional steps required to make the target compound are described in the preparation of Example 1.
The following compounds were prepared using the methodology described for the preparation of compound 10 using the appropriate Grignard reagent to introduce suitable bromoacetals to generate alternate chain lengths (m) 73 Compound R2 m 11 4-biphenyl 8 12 naphthyl 8 13 3-biphenyl 8 14 2-pyridinyl 8 3,5-difluorophenyl 8 16 3,4,5-triflurophenyl 8 17 2-methylphenyl 8 18 3-methylphenyl 8 19 4-methylphenyl 8 4-fluorophenyl 8 1B 3-fluorophenyl 8 2B 3-chlorophenyl 8 1C cyclohexyl 8 2C 2-thienyl 5 3C 3-thienyl 5 Example 21 (R)-Quinuclidinyl (3-(9-(2-(4-hydroxyoxo-2,3- dihydrobenzo[d]thiazolyl)ethylamino)nonyloxy)phenyl)- (phenyl)methylcarbamate (compound 21) N H OH O H N O O N N H S O The preparation of compound 21 requires 7-(2-aminoethyl) hydroxybenzo[d]thiazol-2(3H)-one hydrobromide (prepared as described in Organic Process Research & Development 2004, 8, 628-642) replacing (R)(2-aminohydroxyethyl)hydroxyquinolin-2(1H)-one hydrochloride in Example 1 Step 7. The additional steps required to make the title compound are described in Example 1. 74 Scheme for Example 22 LiAlH4 , THF O O N HCl Cl Ph2PON3 , DBU, toluene Pyridine i) HCl THF ii) NaB(OAc)3H, AcOH NEt3 , MeOH O O HO O BH3 -Me2S THF O O HO DIAD, Ph3P, THF O Ph HO O Ph O O O NaBH4 MeOH OH Ph O O O N3 Ph O O O NH2 Ph O O O N H O O O N O O N H HO N H OH O O H N O N O Example 22 (R)-Quinuclidinyl (3-(4-(2-((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethylamino)ethyl)benzyloxy)phenyl)(phenyl)- methylcarbamate (compound 22) N H HO N H OH O O H N O N O Step 1; (4-((1,3-Dioxolanyl)methyl)phenyl)methanol O O HO To a cooled (0°C) solution of 4-((1,3-dioxolanyl)methyl)benzoic acid (1.02 g, 4.92 mmol) in anhydrous THF (63.5 mL), a solution of borane dimethylsulfide complex (2.0 M in THF, 12.29 mL, 24.59 mmol) was added dropwise. The reaction mixture was stirred at this temperature for 5 minutes and then the coolant removed. The reaction mixture was stirred at RT for 16 hours. The reaction mixture was cooled to 0°C and methanol (1 mL) was 75 added. The reaction mixture was diluted with water and saturated aqueous sodium hydrogen carbonate and then extracted with ethyl acetate (x 2). The combined organic extracts were washed with brine, dried (magnesium sulphate) filtered and concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 0-50% ethyl acetate in iso-hexane to afford the title compound (0.936 g, 98%).
¹H NMR (400 MHz, CDCl3): δ 7.29 (m, 4 H), 5.08-5.02 (m, 1 H), 4.67 (d, J = 5.97 Hz, 2 H), 4.00-3.78 (m, 4 H), 2.97 (d, J = 4.82 Hz, 2 H), 1.61-1.58 (m, 1H).
Step 2; (3-(4-((1,3-Dioxolanyl)methyl)benzyloxy)phenyl)- (phenyl)methanone O Ph O O O To a cooled (0°C) solution of (4-((1,3-dioxolan yl)methyl)phenyl)methanol (0.45 g, 2.317 mmol), 3-hydroxybenzophenone (0.551 g, 2.78 mmol) and triphenylphosphine (0.729 g, 2.78 mmol) in anhydrous THF, di-iso-propylazodicarboxylate (1.027 mL, 2.78 mmol) was added dropwise. The reaction mixture was allowed to warm to RT and stirred at this temperature for 16 hours. The reaction mixture was diluted with ethyl acetate and washed with 10% aqueous potassium carbonate, brine and dried (magnesium sulphate). The suspension was filtered and concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 100% iso-hexane to 25% ethyl acetate in iso-hexane to afford the title compound (1.022 g, >100%).
¹H NMR (400 MHz, CDCl3): δ 7.82-7.76 (m, 2 H), 7.63-7.55 (m, 1 H), 7.51-7.16 (m, 10 H), 5.11-5.05 (m, 3 H), 3.98-3.92 (m, 2 H), 3.87-3.82 (m, 2 H), 2.98 (d, J = 4.8 Hz, 2 H).
The title compound was prepared as described in Example 1 with (3-(4- 76 ((1,3-Dioxolanyl)methyl)benzyloxy)phenyl)(phenyl)methanone replacing (3-(8-(1,3-Dioxolanyl)octyloxy)phenyl)(phenyl)methanone in Step 2.
The additional steps required to make the target compound are described in Example 1.
Example 23 (R)-Quinuclidinyl (3-(2-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)ethyl)phenyl)(phenyl)methylcarbamate (compound 23) N H N H O OH HO H N O O N Step 1; 3-((1,3-Dioxolanyl)methyl)benzaldehyde O O O To a solution of (3-((1,3-dioxolanyl)methyl)phenyl)methanol (prepared as in Example 22, Step 1 with 3-((1,3-dioxolan yl)methyl)benzoic acid replacing 4-((1,3-dioxolanyl)methyl)benzoic acid; 0.47 g, 2.42 mmol) in 1,4-dioxane (8 mL), manganese (IV) oxide (2.35 g) was added. The resulting suspension was heated at 100°C for 16 hours. The reaction mixture was allowed to cool and the suspension filtered through a pad of celite. The celite pad was washed with ethyl acetate and the filtrate evaporated at reduced pressure to afford the title compound (0.352 g, 76%).
¹H NMR (400 MHz, CDCl3): δ 10.01 (s, 1 H), 7.79-7.74 (m, 2 H), 7.56 (dt, J = 7.6, 1.5 Hz, 1 H), 7.51-7.43 (m, 1 H), 5.13-5.08 (m, 1 H), 3.96-3.81 (m, 4 H), 3.06 (d, J = 4.6 Hz, 2 H).
The title compound was prepared as described in Example 2 with 3- ((1,3-dioxolanyl)methyl)benzaldehyde replacing 3-(8-(1,3-dioxolan 77 yl)octyloxy)benzaldehyde in Step 2. The additional steps required to make the target compound are described in Example 1.
Example 24 (3R)((((3-((6-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(phenyl)methyl)- carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium To a solution of (R)-quinuclidinyl (3-(6-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)hexyloxy)- phenyl)(phenyl)methylcarbamate (Example 4, 0.02 g, 0.03 mmol) in methanol (0.5 mL) was added a solution of 2-bromoacetophenone (0.007 g, 0.04 mmol) in methanol (0.5 mL). The reaction mixture was stirred at RT for 1 hour.
Further 2-bromoacetophenone (0.007 g, 0.04 mmol) added and the reaction continued for 15 minutes. The solvent was evaporated at reduced pressure.
The residue was purified by reverse phase preparative HPLC to afford the title compound (0.010 g, 43%).
Example 25 (R)-quinuclidinyl (3-(3-(2-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)ethyl)benzyloxy)phenyl)(phenyl)- methylcarbamate formate (compound 3B) 78 The title compound was prepared as described in Example 22 with 3- ((1,3-dioxolanyl)methyl)benzoic acid replacing 4-((1,3-dioxolan yl)methyl)benzoic acid in Step 1. The additional steps required to make the target compound are described in the preparation of Example 1.
Example 26 (3R)((((3-((4-(2-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)ethyl)benzyl)oxy)phenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 4B) N H O OH HO N H O H N O N + O O The title compound was prepared as described in Example 24 with (R)- quinuclidinyl (3-(4-(2-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)ethyl)benzyloxy)phenyl)(phenyl)- methylcarbamate (Example 22) replacing (R)-quinuclidinyl (3-(6-((R) hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyloxy)-phenyl)(phenyl)methylcarbamate.
Example 27 (3R)((((3-chlorophenyl)(3-((9-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)methyl)- carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 5B) The title compound was prepared as described in Example 24 with ((R)-quinuclidinyl (3-chlorophenyl)(3-(9-((R)hydroxy(8-hydroxy- 79 2-oxo-1,2-dihydroquinolinyl)ethylamino)nonyloxy)phenyl)- methylcarbamate (Example 26) replacing (R)-quinuclidinyl (3-(6-((R) hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyloxy)phenyl)-(phenyl)methylcarbamate.
Example 28 (3R)((((3-bromo((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)- carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 6B) N H HO N H O OH O H N O O N Br O Step 1; Benzyl 3-bromohydroxybenzoate To a stirred solution of 3-bromohydroxybenzoic acid (2 g, 9.22 mmol) in dimethyl formamide (50 mL) was added potassium carbonate (1.27 g, 9.21 mmol) and stirred at 0°C for 20 minutes. Benzyl bromide (1.1 mL, 9.25 mmol) was added and the reaction mixture allowed to warm to room temperature over 16 hours. The reaction mixture was diluted with water and extracted with ethyl acetate (x 3). The combined organic extracts were washed with brine, dried (magnesium sulphate), filtered and concentrated under reduced pressure to afford the title compound (2.85 g, quantitative yield).
¹H NMR (400 MHz, CDCl3): δ 7.75-7.72 (m, 1 H); 7.51-7.48 (m, 1 H); 7.45-7.34 (m, 5 H); 7.24-7.21 (m, 1 H); 5.34 (s, 2 H) 80 Step 2; Benzyl 3-((8-(1,3-dioxolanyl)octyl)oxy)bromobenzoate To a stirred solution of benzyl 3-bromohydroxybenzoate (2.85 g, 9.22 mmol) in dimethyl formamide (50 mL) was added 2-(8-bromooctyl)-1,3- dioxolane (2.44 g, 9.21 mmol) and potassium carbonate (1.91 g, 13.8 mmol) and stirred at 80°C for 16 hours. The reaction mixture was cooled to room temperature, diluted with water and extracted with ethyl acetate (x 3). The combined organic extracts were washed with brine, dried (magnesium sulphate), filtered and concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 0-7% ethyl acetate in iso-hexane to afford the title compound (2.94 g, 65%).
¹H NMR (400 MHz, CDCl3): δ 7.76-7.75 (m, 1 H); 7.51-7.50 (m, 1 H); 7.45-7.34 (m, 5 H); 7.23-7.22 (m, 1 H); 5.35 (s, 2 H); 4.84 (t, J = 4.8 Hz; 1 H); 4.00-3.94 (m, 4 H); 3.86-3.83 (m, 2 H); 1.80-1.73 (m 2 H); 1.68-1.63 (m, 2 H); 1.44-1.22 (m, 10 H).
Step 3; (3-((8-(1,3-Dioxolanyl)octyl)oxy) bromophenyl)methanol To a solution of benzyl 3-((8-(1,3-dioxolanyl)octyl)oxy) bromobenzoate in tetrahydrofuran (30 mL) at -78°C was added a solution of lithium aluminium hydride in THF (2.0 M, 3.3 mL, 6.60 mmol). The reaction mixture was stirred for 4 hours, then quenched with water (0.25 mL), 2 M sodium hydroxide (0.25 mL) and water (0.75 mL). The coolant was removed and ethyl acetate and magnesium sulphate was added and the mixture stirred at room temperature for 20 minutes. The suspension was filtered, washed with 81 ethyl acetate and the filtrate was concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 0-17% ethyl acetate in iso-hexane to afford the title compound as a 10:7 ratio of product to starting material (1.69 g, 73%).
¹H NMR (400 MHz, CDCl3): δ 7.08 (s, 1 H); 6.97-6.96 (m, 1 H); 6.84 (m, 1 H); 4.84 (t, J = 4.8 Hz, 1 H); 4.66-4.63 (m, 2 H); 3.99-3.89 (m, 4 H); 3.84-3.81 (m, 2 H); 1.79-1.74 (m, 2 H); 1.66-1.63 (m, 2 H); 1.45-1.42 (m, 10 H).
Step 4; 3-((8-(1,3-Dioxolanyl)octyl)oxy)bromobenzaldehyde To a stirred solution of (3-((8-(1,3-dioxolanyl)octyl)oxy) bromophenyl)methanol (1.69 g, 4.36 mmol) in 1,4-dioxane (25 mL) was added magnesium (IV) oxide (1.90 g, 21.9 mmol). The reaction mixture was heated to 100°C for 16 hours. The suspension was filtered, washed with ethyl acetate and the filtrate was concentrated under reduced pressure to afford the title compound (1.25 g, 74%).
¹H NMR (400 MHz, CDCl3): δ 9.89 (s, 1 H); 7.56 (m, 1 H); 7.31 (m, 2 H); 4.85 (t, J = 4.8 Hz, 1 H); 4.10-3.95 (m 4 H); 3.86-3.83 (m, 2 H); 1.82-1.75 (m, 2 H); 1.69-1.63 (m, 2 H); 1.45-1.34 (m, 10 H).
Step 5; (3-((8-(1,3-Dioxolanyl)octyl)oxy) bromophenyl)(phenyl)methanol 82 The title compound was prepared as described in Example 10 Step 2 with 3-((8-(1,3-dioxolanyl)octyl)oxy)bromobenzaldehyde and phenylmagnesium bromide replacing 3-(8-(1,3-dioxolan yl)octyloxy)benzaldehyde and 2-thienylmagnesium bromide respectively.
¹H NMR (400 MHz, CDCl3): δ 7.38-7.27 (m, 5 H); 7.10 (d, J = 1.52 Hz, 1 H); 6.95-6.91 (m, 1 H); 6.87 (s, 1 H); 5.74 (d, J = 3.46 Hz, 1 H); 4.84 (t, J = 4.83 Hz, 1 H); 3.99-3.93 (m, 2 H); 3.90 (t, J = 6.48 Hz, 2 H); 3.87-3.81 (m, 2 H); 2.28 (d, J = 4.43 Hz, 1 H); 1.78-1.60 (m, 4 H); 1.37 (d, J = 34.79 Hz, 10 H).
Step 6; 2-(8-(3-(Azido(phenyl)methyl)bromophenoxy)octyl)-1,3- dioxolane The title compound was prepared as described in Example 1 Step 3 with (3-((8-(1,3-dioxolanyl)octyl)oxy)bromophenyl)(phenyl)methanol replacing (3-(8-(1,3-dioxolanyl)octyloxy)phenyl)(phenyl)methanol.
¹H NMR (400 MHz, CDCl3): δ 7.40-7.19 (m, 5 H); 7.11-6.91 (m, 1 H); 6.97-6.95 (m, 1 H); 6.78 (s, 1 H); 5.61 (s, 1 H); 4.84 (t, J = 4.83 Hz, 1 H); 3.98-3.93 (m, 2 H); 3.92-3.86 (m, 2 H); 3.88-3.82 (m, 2 H); 1.79-1.61 (m, 4 H); 1.53-1.25 (m, 10 H).
Step 7; (3-((8-(1,3-Dioxolanyl)octyl)oxy) bromophenyl)(phenyl)methanamine To a stirred reaction of 2-(8-(3-(Azido(phenyl)methyl) 83 bromophenoxy)octyl)-1,3-dioxolane (1.19 g, 2.45 mmol) in tetrahydrofuran (15 mL) and water (0.3 mL) was added triphenylphosphine (0.71 g, 2.69 mmol). The reaction mixture was heated to 60°C for 16 hours. The reaction mixture was cooled, concentrated and purified by silica gel chromatography eluting with 0-100% ethyl acetate in iso-hexane to afford impure title compound as a colourless oil (0.77 g, 68%).
¹H NMR (400 MHz, CDCl3): δ 7.38-7.29 (m, 5 H); 7.11 (t, J = 1.55 Hz, 1 H); 6.94-6.84 (m, 2 H); 5.12 (s, 1 H); 4.84 (t, J = 4.83 Hz, 1 H); 3.99-3.94 (m, 2 H); 3.93-3.81 (m, 4 H); 1.77-1.60 (m, 4 H); 1.48-1.28 (m, 10 H).
Step 8; (R)-quinuclidinyl ((3-((8-(1,3-dioxolanyl)octyl)oxy) bromophenyl)(phenyl)methyl)carbamate The title compound was prepared as described in Example 1, Step 5 with (3-((8-(1,3-dioxolanyl)octyl)oxy)bromophenyl)(phenyl)- methanamine replacing (3-(8-(1,3-dioxolanyl)octyloxy)phenyl)(phenyl)- methanamine.
Step 9; (R)-quinuclidinyl ((3-bromo((9-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)- (phenyl)methyl)carbamate The title compound was prepared as described in Example 1 Steps 6 and 7 with (R)-quinuclidinyl ((3-((8-(1,3-dioxolanyl)octyl)oxy) bromophenyl)(phenyl)methyl)carbamate replacing (R)-quinuclidinyl (3- (8-(1,3-dioxolanyl)octyloxy)phenyl)(phenyl)methylcarbamate in Step 6 and (R)-Quinuclidinyl ((3-bromo((9-oxononyl)oxy)phenyl)(phenyl)- 84 methyl)carbamate replacing (R)-quinuclidinyl (3-(9-oxononyloxy)- phenyl)(phenyl)methylcarbamate in Step 7.
Step 10; (3R)((((3-bromo((9-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 6B) N H HO N H O OH O H N O O N Br O The title compound was prepared as described in Example 24 with (R)- quinuclidinyl ((3-bromo((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)- carbamate replacing (R)-quinuclidinyl (3-(6-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)hexyloxy)phenyl)- (phenyl)methylcarbamate.
Example 29 (R)-quinuclidinyl (2-chloro(9-((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(phenyl)- methylcarbamate (compound 7B) Step 1; 3-((8-(1,3-Dioxolanyl)octyl)oxy)chlorobenzaldehyde O O O Cl H O 85 The title compound was prepared as described in Example 10 Step 1 with 2-chlorohydroxybenzaldehyde replacing 3-hydroxybenzaldehyde.
¹H NMR (400 MHz, CDCl3-d): δ 10.53 (d, J = 0.92 Hz, 1 H); 7.51 (d, J = 7.79 Hz, 1 H); 7.35-7.26 (m, 1 H); 7.15 (d, J = 8.16 Hz, 1 H); 4.86-4.81 (m, 1 H); 4.09-4.02 (m, 2 H); 4.00-3.93 (m, 2 H); 3.91-3.81 (m, 2 H); 1.91-1.76 (m, 3 H); 1.70-1.19 (m, 11 H).
Step 2; (R)-quinuclidinyl (2-chloro(9-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)nonyloxy)phenyl)- (phenyl)methylcarbamate (compound 7B) The title compound was prepared as in Example 10 with 3-((8-(1,3- dioxolanyl)octyl)oxy)chlorobenzaldehyde replacing 3-((8-(1,3- dioxolanyl)octyl)oxy)-benzaldehyde in Step 2 and using the subsequent steps described in Example 1.
Example 30 (R)-quinuclidinyl ((2,6-difluoro((9-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)- (phenyl)methyl)carbamate (compound 8B) The title compound was prepared as described for Example 29 from the commercially available 2,6-difluorohydroxybenzaldehyde. 86 Example 31 (R)-quinuclidinyl ((2-bromo((9-(((R)hydroxy(8-hydroxy2-oxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)- (phenyl)methyl)carbamate (compound 9B) The title compound was prepared as described for Example 19 from the commercially available 2-bromohydroxybenzaldehyde.
Example 32 (3R)((((2-chloro((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)- carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 10B) N H HO N H O OH O H N O O N Cl O The title compound was prepared as described in Example 24 with (R)- quinuclidinyl (2-chloro(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(phenyl)- methylcarbamate (Example 31) replacing (R)-quinuclidinyl (3-(6-((R) hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyloxy)phenyl)(phenyl)methylcarbamate.
Example 33 (3R)((((2,6-difluoro((9-(((R)hydroxy(8-hydroxyoxo- 87 1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)- carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 11B) The title compound was prepared as described in Example 24 with (R)- quinuclidinyl ((2,6-difluoro((9-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)- carbamate (Example 30) replacing (R)-quinuclidinyl (3-(6-((R) hydroxy(8-hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)- hexyloxy)phenyl)(phenyl)methylcarbamate.
Example 34 (3R)((((2-bromo((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)- carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 12B) The title compound was prepared as described in Example 24 with (R)- quinuclidinyl ((2-bromo((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)- carbamate replacing (R)-quinuclidinyl (3-(6-((R)hydroxy(8- 88 hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)hexyloxy)phenyl)- (phenyl)methylcarbamate.
Example 35 (3R)((((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)methylphenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 13B) N H HO N H O OH O H N O O N O Step 1; (3-((8-(1,3-dioxolanyl)octyl)oxy)methylphenyl)- methanol To a stirred solution of 5-(hydroxymethyl)methylphenol (0.57 g, 4.15 mmol) in dimethyl formamide (15 mL) was added 2-(8-bromooctyl)-1,3- dioxolane (1.00 g, 3.77 mmol) and potassium carbonate (0.63 g, 4.57 mmol) and stirred at 80ºC for 16 hours. The reaction mixture was cooled to room temperature, diluted with water and extracted with ethyl acetate (x 3). The combined organic extracts were washed with brine, dried (magnesium sulphate), filtered and concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 0-7% ethyl acetate in iso-hexane to afford the title compound (0.5 g, 41%).
¹H NMR (400 MHz, DMSO-d6): δ 7.06 (d, J = 8 Hz, 1 H); 6.86 (s, 1 H); 6.77 (d, J = 8 Hz, 1 H); 5.10 (d, J = 5.6 Hz, 1 H); 4.75 (t, J = 4.8 Hz, 1 H); 4.44 (d, J = 5.6 Hz, 2 H); 3.94 (t, J = 6.4 Hz, 2 H); 3.86-3.84 (m, 2 H); 3.76- 89 3.74 (m, 2 H); 2.11 (s, 3 H); 1.73 (m, 2 H); 1.53 (m, 2 H); 1.35-1.30 (m, 10 H).
Step 2; (3R)((((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)methylphenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 13B) N H HO N H O OH O H N O O N O The title compound was prepared as described in Example 18 Steps 4 to 9 with (3-((8-(1,3-dioxolanyl)octyl)oxy)methylphenyl)methanol replacing (3-((8-(1,3-dioxolanyl)octyl)oxy)bromophenyl)methanol in Step 4 and the products used in the subsequent steps.
Example 36 (R)-quinuclidinyl ((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy) methoxyphenyl)(phenyl)methyl)carbamate (compound 14B) The title compound was prepared as described for Example 29 from the commercially available 3-hydroxymethoxybenzaldehyde.
Example 37 (R)-quinuclidinyl ((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)methoxyphenyl)(phenyl)- 90 methyl)carbamate (compound 15B) Step 1; Benzyl 3-((8-(1,3-dioxolanyl)octyl)oxy) hydroxybenzoate The title compound was prepared as described in Example 28 Step 1 and 2 with 3,5-dihydroxybenzoic acid replacing 5-bromohydroxybenzoic acid in Step 1 and the product used in the subsequent step.
Step 2; Benzyl 3-((8-(1,3-dioxolanyl)octyl)oxy) methoxybenzoate To an ice-cooled solution of benzyl 3-((8-(1,3-dioxolan yl)octyl)oxy)hydroxybenzoate (1.94 g, 4.53 mmol) in dimethyl formamide (25 mL) was added potassium carbonate (0.93 g, 6.75 mmol) followed by iodomethane (0.42 mL, 6.75 mmol). The reaction mixture was allowed to warm to room temperature over 16 hours and stood at room temperature for 3 days. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic extracts were washed with brine, dried (MgSO4), filtered and concentrated under reduced pressure to afford the title compound (1.76 g, 88%). 1NMR (400 MHz, CDCl3-d): 7.45-7.32 (m, 5 H); 7.20-7.18 (m, 2 H); 6.64-6.63 (m, 1 H); 5.35 (s, 2 H); 4.84 (t, J = 4.8 Hz, 1 H); 4.10-3.92 (m, 4 H); 91 3.86-3.82 (m, 5 H); 1.80-1.73 (m, 2 H); 1.68-1.63 (m, 2 H); 1.46-1.34 (m, 10 H).
Step 3; (R)-quinuclidinyl ((3-((9-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy) methoxyphenyl)(phenyl)methyl)carbamate (compound 15B) The title compound was prepared as described in Example 28 Steps 3 through 9 with benzyl 3-((8-(1,3-dioxolanyl)octyl)oxy) methoxybenzoate replacing benzyl 3-((8-(1,3-dioxolanyl)octyl)oxy) bromobenzoate in Step 3 and the product used in the subsequent steps.
Example 38 (3R)((((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)methoxyphenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 16B) The title compound was prepared as described in Example 24 with (R)- quinuclidinyl ((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)methoxyphenyl)(phenyl)- methyl)carbamate (Example 36) replacing (R)-quinuclidinyl (3-(6-((R)- 2-hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 92 yl)ethylamino)hexyloxy)phenyl)(phenyl)methylcarbamate.
Example 39 (3R)((((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy) methoxyphenyl)(phenyl)methyl)carbamoyl)oxy)(2-oxo phenylethyl)quinuclidinium (compound 17B) The title compound was prepared as described in Example 24 with (R)- quinuclidinyl ((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)methoxyphenyl)(phenyl)- methyl)carbamate (Example 36) replacing (R)-quinuclidinyl (3-(6-((R)- 2-hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyloxy)phenyl)(phenyl)methylcarbamate.
Example 40 (3R)((((5-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)-[1,1'-biphenyl]yl)- (phenyl)methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 18B) Step 1; (R)-quinuclidinyl ((5-((8-(1,3-dioxolanyl)octyl)oxy)- 93 [1,1'-biphenyl]yl)(phenyl)methyl)carbamate To a stirred solution of (R)-quinuclidinyl ((3-((8-(1,3-dioxolan yl)octyl)oxy)bromophenyl)(phenyl)methyl)carbamate (0.2 g, 0.33 mmol) (prepared in Example 28 Step 8) in toluene (4 mL) and water (1 mL) was added phenyl boronic acid (0.04 g, 0.33 mmol), sodium carbonate (0.07 g, 0.66 mmol) and tetrakis (triphenylphosphine) palladium (0) (0.04 g, 0.03 mmol). The reaction mixture was heated in the microwave at 120°C for 30 minutes. The solvent was removed under reduced pressure, diluted with water and extracted with ethyl acetate (x 3). The combined organic extracts were dried (sodium sulphate), filtered and solvent removed under reduced pressure.
The crude material was purified by silica gel chromatography eluting with 0- % methanol in ethyl acetate to afford the title compound as a colourless oil (0.14 g, 71%).
¹H NMR (400 MHz, CDCl3): δ 7.53 (d, J = 7.56 Hz, 2 H); 7.44-7.38 (m, 2 H); 7.38-7.27 (m, 6 H); 7.06 (s, 1 H); 7.01 (s, 1 H); 6.78 (s, 1 H); 5.95 (br s, 1 H); 5.4 (br s, 1 H); 4.86-4.81 (t, J = 4.81 Hz, 1 H); 4.77-4.71 (m, 1 H); 3.99- 3.92 (m, 4 H); 3.86-3.81 (m, 2 H); 3.2-2.6 (m, 6 H); 2.03 (s, 1 H); 1.80-1.71 (m, 2 H); 1.7-1.3 (m, 15 H). 94 Step 2; 3R)((((5-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)-[1,1'-biphenyl] yl)(phenyl)methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidin ium (compound 18B) The title compound was prepared as described in Example 28 Steps 9 and 10 with (R)-quinuclidinyl ((5-((8-(1,3-dioxolanyl)octyl)oxy)-[1,1'- biphenyl]yl)(phenyl)methyl)carbamate replacing (R)-quinuclidinyl ((3-bromo((9-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin10 5-yl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)carbamate in Step 9 and the product used in the subsequent steps.
Also prepared by the method of Example 40 Compound R R4 19B 2-thienyl N Example 41 (3R)((((3-((3-(4-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)butoxy)benzyl)oxy)phenyl)- (phenyl)methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 95 (compound 20B) Step 1; (3-(3-(1,3-Dioxolanyl)propoxy)phenyl)methanol To an ice-cooled solution of 3-(3-(1,3-dioxolan yl)propoxy)benzaldehyde (prepared as in Example 10; Step 1) (3.08 g, 13.1 mmol) in ethanol (66 mL) was added sodium borohydride (1.98 g, 52.4 mmol). The reaction mixture was allowed to warm to ambient temperature and stirred at ambient temperature for 16 hours. The reaction mixture was carefully quenched with saturated aqueous ammonium chloride and extracted twice with DCM. The combined organic phases were poured through a hydrophobic column and the solvent evaporated at reduced pressure to afford the title compound as a colourless oil (2.96 g, 95%).
¹H NMR (400 MHz, CDCl3): δ 7.25 (m, 1 H), 6.93-6.88 (m, 2 H), 6.82 (m, 1 H), 4.93 (m, 1 H), 4.66 (m, 2 H), 4.02-3.92 (m, 4 H), 3.87 (m, 2 H), 1.96-1.77 (m, 5 H).
Step 2; (R)-Quinuclidinyl ((3-((3-(4-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)butoxy)benzyl)- oxy)phenyl)(phenyl)methyl)carbamate The title compound was prepared as described in Example 22 with (3-(3- (1,3-dioxolanyl)propoxy)phenyl)methanol replacing (4-((1,3-dioxolan yl)methyl)phenyl)methanol in Step 2. The additional steps required to make the 96 target compound are described in the preparation of Example 1.
¹H NMR (400 MHz, CD3OD): δ 8.56 (s, 1 H); 8.38 (d, J = 9.9 Hz, 1 H); 7.33-7.20 (m, 8 H); 7.07-6.85 (m, 7 H); 6.70-6.65 (m, 1 H); 5.87 (s, 1 H); .43-5.36 (m, 1 H); 5.03 (s, 2 H); 4.92 (m, 1H); 4.08-4.02 (m, 2 H); 3.51-3.50 (m, 1 H); 3.27-3.06 (m, 9 H); 2.30-1.60 (m, 9 H).
Step 3; (3R)((((3-((3-(4-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)butoxy)benzyl)oxy)phenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium The title compound was prepared as described in Example 24 with (R)- quinuclidinyl ((3-((3-(4-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)butoxy)benzyl)oxy)phenyl)- (phenyl)methyl)carbamate replacing (R)-quinuclidinyl (3-(6-((R) hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyloxy)phenyl)(phenyl)methylcarbamate.
Example 42 (3R)((((3-((3-(4-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)butoxy)benzyl)oxy)phenyl)- (phenyl)methyl)carbamoyl)oxy)(2-phenoxyethyl)quinuclidinium (compound 21B) 97 The title compound was prepared as in Example 24 with (R)-quinuclidin3-yl ((3-((3-(4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butoxy)benzyl)oxy)phenyl)-(phenyl)methyl)carbamate replacing (R)-quinuclidinyl (3-(6-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)-hexyloxy)phenyl)(phenyl)methylcarbamate and β-bromophenetole replacing 2-bromoacetophenone.
Example 43 (3R)((((3-((3-((5-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)pentyl)oxy)benzyl)oxy)phenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 22B) The title compound was prepared as described in Example 22 with (3-(4- (1,3-dioxolanyl)butyloxy)phenyl)methanol replacing (3-(3-(1,3-dioxolan yl)propoxy)phenyl)methanol in Step 2. The additional steps required to make the target compound are described in the preparation of Example 1 and Example 44.
Example 44 (3R)((((3-((3-((5-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)pentyl)oxy)benzyl)oxy)phenyl)- (phenyl)methyl)carbamoyl)oxy)(2-phenoxyethyl)quinuclidinium (compound 23B) The title compound was prepared as in Example 24 with (R)- 98 quinuclidinyl ((3-((3-((5-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)pentyl)oxy)benzyl)oxy)phenyl)- (phenyl)methyl)carbamate replacing (R)-quinuclidinyl (3-(6-((R) hydroxy(8-hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)- hexyloxy)phenyl)(phenyl)methylcarbamate and β-bromophenetole replacing 2-bromoacetophenone.
Example 45 (R)-quinuclidinyl (3-fluorophenyl)(3-(6-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)hexyloxy)- phenyl)methylcarbamate (compound 24B) Step 1; 3-((5-(1,3-dioxolanyl)pentyl)oxy)benzaldehyde The title compound was prepared as described in Example 10 Step 1 with 2-(5-bromopentyl)-1,3-dioxolane replacing 2-(8-bromooctyl)-1,3- dioxolane.
¹H NMR (400 MHz, CDCl3): δ 9.99-9.92 (m, 1 H); 7.47-7.36 (m, 3 H); 7.19-7.13 (m, 1 H); 4.89-4.83 (m, 1 H); 4.04-3.82 (m, 6 H); 1.90-1.78 (m, 2 H); 1.74-1.65 (m, 2 H); 1.58-1.48 (m, 4 H).
Step 2; (3-((5-(1,3-dioxolanyl)pentyl)oxy)phenyl)(3- fluorophenyl)methanol 99 The title compound was prepared as described in Example 10 Step 2 with 3-fluorophenylmagnesium bromide and 3-((5-(1,3-dioxolan yl)pentyl)oxy)benzaldehyde replacing 2-thienylmagnesium bromide and 3-(8- (1,3-dioxolanyl)octyloxy)benzaldehyde respectively.
¹H NMR (400 MHz, CDCl3): δ 7.32- 7.08 (m, 4 H); 6.98-6.89 (m, 3 H); 6.87-6.77 (m, 1 H); 5.79-5.75 (m, 1 H); 4.88-4.82 (m, 1 H); 4.01-3.78 (m, 6 H); 2.35-2.25 (m, 1 H); 1.82-1.65 (m, 4 H); 1.54-1.44 (m, 4 H).
Step 3; (R)-quinuclidinyl (3-fluorophenyl)(3-(6-((R)hydroxy (8-hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)hexyloxy)- phenyl)methylcarbamate The additional steps required to prepare the title compound are described in Example 1 Steps 3 through 7.
Example 46 (3R)((((3-((5-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)pentyl)oxy)phenyl)(phenyl)- methyl)carbamoyl)oxy)(4-phenylbutyl)quinuclidinium (compound 25B) The title compound was prepared as in Example 24 with (R)- quinuclidinyl (3-(5-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)pentyloxy)phenyl)(phenyl)- methylcarbamate (Example 5) replacing (R)-quinuclidinyl (3-(6-((R) 100 hydroxy(8-hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)- hexyloxy)phenyl)(phenyl)methylcarbamate and (4-bromobutyl)benzene replacing 2-bromoacetophenone.
Example 47 (R)-Quinuclidinyl (3-fluorophenyl)(3-(3-(2-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)ethyl)benzyloxy)- phenyl)methylcarbamate (compound 26B) Step 1; 3-((3-((1,3-Dioxolanyl)methyl)benzyl)oxy)benzaldehyde The title compound was prepared as described in Example 22 with (3- ((1,3-dioxolanyl)methyl)phenyl)methanol and 3-hydroxybenzaldehyde replacing (4-((1,3-dioxolanyl)methyl)phenyl)methanol and 3-hydroxybenzophenone respectively in Step 2 Step 2; (3-((3-((1,3-Dioxolanyl)methyl)benzyl)oxy)phenyl)(3- fluorophenyl)methanol The title compound was prepared as described in Example 10 Step 2 with 3-fluorophenylmagnesium bromide and 3-((3-((1,3-dioxolan yl)methyl)benzyl)oxy)benzaldehyde replacing 2-thienylmagnesium bromide and 3-(8-(1,3-dioxolanyl)octyloxy)benzaldehyde respectively.
¹H NMR (400 MHz, CDCl3): δ 7.34-7.21 (m, 6 H); 7.13-7.06 (m, 2 H); 7.00 (t, J = 2.0 Hz, 1 H); 6.97-6.87 (m, 3 H); 5.77 (d, J = 3.5 Hz, 1 H); 101 .10-4.99 (m, 3 H); 3.94-3.87 (m, 2 H); 3.88-3.78 (m, 2 H); 2.97 (d, J = 4.8 Hz, 2 H); 2.35 (d, J = 3.5 Hz, 1 H).
Step 3; (R)-Quinuclidinyl (3-fluorophenyl)(3-(3-(2-((R) hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)ethyl)benzyloxy)phenyl)methylcarbamate (compound 27B) The title compound was prepared using the additional steps described in Example 1 Steps 3 through 7.
Example 48 (3R)((((3-fluorophenyl)(3-((3-(2-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)ethyl)benzyl)oxy)phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 27B) The title compound was prepared as in Example 24 with (R)- quinuclidinyl (3-fluorophenyl)(3-(3-(2-((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethylamino)ethyl)benzyloxy)- phenyl)methylcarbamate replacing (R)-quinuclidinyl (3-(6-((R) hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyloxy)phenyl)(phenyl)methylcarbamate. 102 Example 49 (3R)((((3-((4-((((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)methyl)benzyl)oxy)phenyl)(phenyl)- methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 28B) Step 1; (4-(1,3-Dioxolanyl)phenyl)methanol A mixture of terephthaldehyde (5.4 g, 40 mmol), para-toluenesulfonic acid – monohydrate (0.4 g, 2 mmol) and ethylene glycol in toluene (80 mL) was heated at 110°C for 4 hours. The reaction mixture was allowed to cool and was washed with saturated sodium hydrogen carbonate and dried with anhydrous magnesium sulphate. The filtrate was evaporated at reduced pressure to afford a oil. The oil was dissolved in ethanol (200 mL) and then the reaction mixture cooled to 0°C. Sodium borohydride (5.9 g, 160 mmol) was added portionwise and the resultant reaction mixture allowed to warm to ambient temperature over 16 hours. The reaction mixture was quenched with saturated sodium hydrogen carbonate and subsequently extracted twice with ethyl acetate. The combined organic extracts were dried with anhydrous magnesium sulphate and the solvent evaporated at reduced pressure. The crude material was purified by silica gel chromatography eluting with 100% iso-hexane to 50% ethyl acetate in isohexane to afford the title compound as a colourless oil (3.4 g, 48%).
¹H NMR (400 MHz, CDCl3): δ 7.47 (d, J = 8 Hz, 2 H); 7.37 (d, J = 8 Hz, 2 H); 5.81 (s, 1 H); 4.69 (d, J = 5.6 Hz, 2 H); 4.14 (m, 2 H); 4.05 (m, 2 H), 103 1.83 (d, J = 6 Hz, 1 H).
Step 2; (3-((4-(1,3-Dioxolanyl)benzyl)oxy)phenyl)- (phenyl)methanone The title compound was prepared as described in Example 22 with (4- (1,3-dioxolanyl)phenyl)methanol replacing (4-((1,3-dioxolan yl)methyl)phenyl)methanol in Step 2.
¹H NMR (400 MHz, CDCl3): δ 7.79-7.76 (m, 2 H); 7.58 (m, 1 H); 7.52-7.35 (m, 9 H); 7.20 (m, 1 H); 5.83 (s, 1 H); 5.13 (s, 2 H); 4.15 (m, 2 H); 4.06 (m, 2 H).
Step 3; (R)-quinuclidinyl ((3-((4-((((R)hydroxy(8-hydroxy2-oxo-1,2-dihydroquinolinyl)ethyl)amino)methyl)benzyl)oxy)phenyl)- (phenyl)methyl)carbamate The title compound was prepared using the additional steps described in Example 1 Steps 3 through 7.
¹H NMR (400 MHz, DMSO-d6): δ 8.37 (m, 1 H); 8.31 (s, 2 H); 8.16 (m, 1 H); 7.44-7.42 (m, 4 H); 7.38-7.34 (m, 5 H); 7.30-7.26 (m, 2 H); 7.13 (d, J = 8.4 Hz, 1 H); 7.08 (s, 1 H); 6.99-6.92 (m, 3 H); 6.55 (d, J = 10 Hz, 1 H); 5.87 (d, J = 9.6 Hz, 1 H); 5.21 (m, 1 H); 5.09 (s, 2 H); 4.72 (m, 1 H); 3.93 (s, 2 H); 3.32 (m, 1 H); 2.95-2.73 (m, 6 H); 2.06 (s, 1 H); 1.92 (s, 1 H); 1.74-1.51 (m, 3 H) Step 4; (3R)((3-(4-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)methyl)benzyloxy)phenyl)(phenyl)- methylcarbamoyloxy)(2-oxophenylethyl) 104 azoniabicyclo[2.2.2]octane The title compound was prepared as in Example 24 with ((R)- quinuclidinyl ((3-((4-((((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)methyl)benzyl)oxy)phenyl)(phenyl)- methyl)carbamate replacing (R)-quinuclidinyl (3-(6-((R)hydroxy (8-hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)hexyloxy)phenyl)- (phenyl)methylcarbamate.
Example 50 (R)-Quinuclidinyl (3-((4'-(2-((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethylamino)ethyl)biphenyl yl)methoxy)phenyl)(phenyl)methylcarbamate (compound 29B) Step 1; 2-(4-Bromobenzyl)-1,3-dioxolane To a cooled (0°C) solution of 4-bromophenethylalcohol (3.9 g, 19.4 mmol) in DCM (50 mL) was added the Dess-Martin reagent (8.22 g, 19.4 mmol). After 10 minutes the coolant was removed and the reaction mixture was stirred at ambient temperature for 2 hours. The reaction mixture was quenched with 10% aqueous potassium carbonate and the mixture separated.
The aqueous phase was extracted with further DCM (x 2) and the combined 105 organic phases were dried with anhydrous magnesium sulphate and the solvent evaporated at reduced pressure. The crude material was purified by silica gel chromatography eluting with 100% iso-hexane to 50% ethyl acetate in isohexane to afford a oil. The oil was dissolved in toluene (35 mL), para5 toluenesulfonic acid – monohydrate (0.1 g, 0.52 mmol) and ethylene glycol (5.3 mL, 94.2 mmol) was added and the mixture heated at reflux under Dean and Stark conditions for 2 hours. The solvent was evaporated at reduced pressure and the residue dissolved in ethyl acetate. The solution was washed with 10% aqueous potassium carbonate, dried with anhydrous magnesium sulphate and the solvent evaporated at reduced pressure. The crude material was purified by silica gel chromatography eluting with 100% iso-hexane to 50% ethyl acetate in iso-hexane to afford an oil (2.3 g, 49%).
¹H NMR (400 MHz, CDCl3): δ 7.52-7.36 (m, 2 H); 7.19-7.06 (m, 2 H); 5.03 (t, J = 4.6 Hz, 1 H); 3.95-3.85 (m, 2 H); 3.86-3.76 (m, 2 H); 2.93-2.86 (m, 2 H).
Step 2; (4'-((1,3-Dioxolanyl)methyl)-[1,1'-biphenyl]yl)methanol A mixture of 2-(4-bromobenzyl)-1,3-dioxolane (2.0 g, 8.2 mmol), 3-formylboronic acid (2.45 g, 16.4 mmol), tetrakis-(triphenylphosphine)- palladium (0) (0.763 g, 0.66 mmol) and sodium carbonate (1.74 g, 16.4 mmol) in dioxane/water (15 mL / 3 mL) in a microwave vessel was degassed in a stream of nitrogen for 10 minutes. The vessel was sealed and heated in the microwave at 125°C for 30 minutes. The solvent was decanted off and the solid residues washed with ethyl acetate. The organic phases were combined and the solvent evaporated at reduced pressure. The crude material was purified by silica gel chromatography eluting with 100% iso-hexane to 50% ethyl acetate in iso-hexane to afford an oil. The oil was dissolved in methanol 106 (25 mL) and cooled to 0°C. Sodium borohydride (0.393 g, 10.4 mmol) was added portion-wise and the reaction mixture was stirred at 0°C for 30 minutes followed by 1 hour at ambient temperature. The reaction mixture was quenched with water and extracted twice with ethyl acetate. The combined organic extracts were dried with anhydrous magnesium sulphate and the solvent evaporated at reduced pressure. The crude material was purified by silica gel chromatography eluting with 100% iso-hexane to 100% ethyl acetate in iso-hexane to afford the title compound (1.16 g, 52%).
¹H NMR (400 MHz, CDCl3): δ 7.58-7.45 (m, 4 H); 7.44-7.30 (m, 4 H); 5.09 (t, J = 4.8 Hz, 1 H); 4.73 (d, J = 5.0 Hz, 2 H); 3.99-3.83 (m, 4 H); 3.00 (d, J = 4.8 Hz, 2 H); 2.05-1.98 (m, 1 H).
Step 3; tert-butyl ((3-((4'-((1,3-dioxolanyl)methyl)-[1,1'- biphenyl]yl)methoxy)phenyl)(phenyl)methyl)carbamate The title compound was prepared as described in Example 22 Step 2 with (4'-((1,3-dioxolanyl)methyl)-[1,1'-biphenyl]yl)methanol and tertbutyl (3-hydroxyphenyl)(phenyl)methylcarbamate replacing (4-((1,3-dioxolan2-yl)methyl)phenyl)methanol and 3-hydroxybenzophenone respectively.
Step 4; (3-((4'-((1,3-dioxolanyl)methyl)-[1,1'-biphenyl] yl)methoxy)phenyl)(phenyl)methanamine hydrochloride To a solution of tert-butyl ((3-((4'-((1,3-dioxolanyl)methyl)-[1,1'- biphenyl]yl)methoxy)phenyl)(phenyl)methyl)carbamate (1.44 g, 2.6 mmol) in methanol (6.5 mL) was added hydrogen chloride in dioxane (6.5 mL). The reaction mixture was stirred at ambient temperature for 16 hours. The solvent was evaporated to afford a mixture of the title compound and the 107 corresponding dimethyl acetal. The material was used in the next step without further purification.
Step 5; (R)-Quinuclidinyl (3-((4'-(2-((R)hydroxy(8-hydroxy2-oxo-1,2-dihydroquinolinyl)ethylamino)ethyl)biphenyl yl)methoxy)phenyl)(phenyl)methylcarbamate (compound 29B) The title compound was prepared using the additional steps described in Example 1 Steps 3 through 7.
Synthetic scheme for the preparation of ester and amide analogues 108 Example 51 (R)-quinuclidinyl ((3-((4-((4-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)butyl)carbamoyl)benzyl)oxy)- phenyl)(phenyl)methyl)carbamate (compound 30B) Step 1; Methyl 4-((3-benzoylphenoxy)methyl)benzoate To a stirred solution of 3-hydroxybenzophenone (1.00 g, 5.04 mmol) in dimethyl formamide (10 mL) was added potassium carbonate (1.05 g, 7.61 mmol) and stirred for 10 minutes at room temperature. Methyl 4- bromobenzoate (1.30 g, 6.05 mmol) in dimethyl formamide (5 mL) was added and the reaction mixture allowed to stir at room temperature for 16 hours. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic extract was washed with brine, dried (MgSO4) and concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 0-17% ethyl acetate in iso-hexane to afford the title compound (1.64 g, 99%).
¹H NMR (400 MHz, CDCl3): δ 8.07 (d, J = 8.4 Hz, 2 H); 7.79 (d, J = 8.4 Hz, 2 H); 7.61-7.57 (m, 1 H); 7.52-7.37 (m, 8 H); 5.18 (s, 2 H); 3.93 (s, 3 H).
Step 2; Methyl 4-((3-(azido(phenyl)methyl)phenoxy)-methyl)benzoate 109 To an ice-cooled suspension of methyl 4-((3- benzoylphenoxy)methyl)benzoate (1.62 g, 4.88 mmol) in methanol (20 mL) was added sodium borohydride (0.27 g, 7.32 mmol). The reaction mixture was allowed to warm to room temperature over 2 hours. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic extracts were washed with brine, dried (MgSO4) and concentrated under reduced pressure to afford an oil. To a solution of the oil in toluene (25 mL) was added diphenylphosphoryl azide (1.26 mL, 5.85 mmol) and 1,8-diazabicyclo[5.4.0]undecene (881 µL, 5.85 mmol). The reaction mixture was stirred at 100°C for 3 hours. The reaction mixture was allowed to cool to room temperature, diluted with ethyl acetate and washed with water, brine, dried (magnesium sulphate), filtered and concentrated. The crude material was purified by silica gel chromatography eluting with 0-10% ethyl acetate in iso-hexane to afford the title compound (1.62 g, 92% over 2 steps).
¹H NMR (400 MHz, CDCl3): δ 8.05-8.03 (m, 2 H); 7.48-7.46 (m, 2 H); 7.39-7.25 (m, 6 H); 6.93-6.88 (m, 3 H); 5.67 (s, 1 H); 5.10 (s, 2 H); 3.92 (s, 3 H).
Step 3: 4-((3-(Azido(phenyl)methyl)phenoxy)methyl)benzoic acid To a stirred suspension of methyl 4-((3- (azido(phenyl)methyl)phenoxy)methyl)benzoate (1 g, 2.79 mmol) in methanol (25 mL) was added 2M sodium hydroxide (25 mL). The reaction was allowed to stir at room temperature for 3 days. Tetrahydrofuran (10 mL) 110 was added to the reaction mixture and stirred at 50°C for 4 hours followed by 16 hours at room temperature. The reaction mixture was acidified with 10% hydrochloric acid, extracted with dichloromethane, dried (sodium sulphate), filtered and concentrated under reduced pressure to give the title compound (1 g, quantitative).
¹H NMR (400 MHz, CDCl3): δ 8.10 (d, J = 8.09 Hz, 2 H); 7.51 (d, J = 8.03 Hz, 2 H); 7.38-7.27 (m, 6 H); 6.95-6.88 (m, 3 H); 5.67 (s, 1 H); 5.12 (s, 2 H).
Step 4; 4-((3-(Azido(phenyl)methyl)phenoxy)methyl)-N-(4,4- diethoxybutyl)benzamide To a stirred solution of 4-((3-(azido(phenyl)methyl)phenoxy)- methyl)benzoic acid (0.5 g, 1.39 mmol) in dimethyl formamide (14 mL) was added 1-ethyl(3-dimethyllaminopropyl)carbodiimide hydrochloride (0.29 g, 1.53 mmol), 2-hydroxypyridine-N-oxide (0.16 g, 1.53 mmol) and triethylamine (0.49 mL. 3.48 mmol). The reaction mixture was stirred at room temperature for 10 minutes. 4-Amino-butyraldehyde diethyl ether (0.27 g, 1.67 mmol) was added and the reaction mixture stirred at room temperature for 16 hours. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic extracts were washed with brine, dried (sodium sulphate), filtered and concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 0-100% ethyl 111 acetate in iso-hexane to afford the title compound as a colourless oil (0.51 g, 73%).
¹H NMR (400 MHz, CDCl3): δ 7.78 (d, J = 8.08 Hz, 2 H); 7.46 (d, J = 7.94 Hz, 2 H); 7.40-7.24 (m, 6 H); 6.94-6.83 (m, 3 H); 6.52 (s, 1 H); 5.67 (s, 1 H); 5.08 (s, 2 H); 4.58-4.48 (m, 1 H); 3.72-3.62 (m, 2 H); 3.56-3.46 (m, 4 H); 1.83-1.69 (m, 4 H); 1.21 (t, J = 7.04 Hz, 6 H).
Step 5; 4-((3-(Amino(phenyl)methyl)phenoxy)methyl)-N-(4,4- diethoxybutyl)benzamide To a solution of 4-((3-(azido(phenyl)methyl)phenoxy)methyl)-N-(4,4- diethoxybutyl)benzamide (0.51 g, 1.03 mmol) in tetrahydrofuran (10 mL) was added polymer supported triphenylphosphine (3 mmol/g, 0.38 g, 1.13 mmol) and water (0.2 mL). The reaction mixture was stirred at 60°C for 16 hours. The reaction mixture was allowed to cool to room temperature, filtered, the filter-cake washed with dichloromethane and concentrated under reduced pressure to give the title compound (0.41 g, 83%).
¹H NMR (400 MHz, CDCl3): δ 7.76 (d, J = 8.04 Hz, 2 H); 7.48 (d, J = .02 Hz, 2 H); 7.37-7.19 (m, 5 H); 7.03 (d, J = 2.34 Hz, 1 H); 6.98 (d, J = 7.60 Hz, 1 H); 6.83 (d, J = 2.79 Hz, 1 H); 6.41 (s, 1 H); 5.18 (s, 1 H); 5.02 (s, 2 H); 4.56-4.50 (m, 1 H); 3.67 (dq, J = 9.43, 7.05 Hz, 2 H); 3.56-3.45 (m, 4 H); 1.89-1.80 (m, 2 H); 1.73 (s, 2 H); 1.21 (t, J = 7.05 Hz, 6 H).
Step 6; (R)-Quinuclidinyl ((3-((4-((4-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)butyl)carbamoyl)- 112 benzyl)oxy)phenyl)(phenyl)methyl)carbamate (compound 30B) The title compound was prepared as described in Example 1 Step 5 through 7 with 4-((3-(Amino(phenyl)methyl)phenoxy)methyl)-N-(4,4- diethoxybutyl)benzamide (3-(8-(1,3-dioxolanyl)octyloxy)phenyl)- (phenyl)methanamine in Step 5 and the product used in the subsequent steps.
Example 52 (R)-quinuclidinyl (3-(4-(3-((R)hydroxy(8-hydroxyoxo10 1,2-dihydroquinolinyl)ethylamino)propylcarbamoyl)benzyloxy)- phenyl)(phenyl)methylcarbamate (compound 31B) The title compound was prepared as described in Example 51 with 3- amino-propylaldehyde diethyl ether replacing 4-amino-butyraldehyde diethyl ether in Step 4 and the product used in the subsequent steps.
Example 53 (3R)((((3-((4-((3-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)propyl)carbamoyl)benzyl)oxy)phenyl)- (phenyl)methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium 113 (compound 32B) N H O OH HO N H N H HN O N + O O O O The title compound was prepared as in Example 24 with (R)- quinuclidinyl (3-(4-(3-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)propylcarbamoyl)benzyloxy)phenyl)- (phenyl)methylcarbamate (Example 52) replacing (R)-quinuclidinyl (3- (6-((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyloxy)phenyl)(phenyl)methylcarbamate.
Example 54 4-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-((3-(phenyl((((R)-quinuclidinyloxy)carbonyl)- amino)methyl)phenoxy)methyl)benzoate (compound 33B) Step 1; 3-(1,3-Dioxolanyl)propyl 4-((3- (azido(phenyl)methyl)phenoxy)methyl)benzoate 114 To a stirred solution of 3-chloropropyl-1,3-dioxolane (0.2 g, 1.35 mmol) in dimethyl formamide (14 mL) was added 4-((3- (azido(phenyl)methyl)phenoxy)methyl)benzoic acid (Example 51 Step 3) (0.5 g, 1.39 mmol) and potassium carbonate (0.38 g, 2.78 mmol). The reaction was allowed to stir at 80°C for 16 hours. The reaction mixture was cooled to room temperature, diluted with water and extracted with ethyl acetate (x 3).
The organic extracts were washed with brine, dried (sodium sulphate), filtered and concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 0-100% ethyl acetate in iso-hexane to afford the title compound (0.63 g, 96%).
¹H NMR (400 MHz, CDCl3): δ 7.53-7.43 (m, 2 H); 7.39-7.25 (m, 8 H); 6.92 (d, J = 5.57 Hz, 3 H); 5.67 (s, 1 H); 5.10 (s, 2 H); 4.94 (t, J = 4.40 Hz, 1 H); 4.40-4.33 (t, J = 6.39 Hz, 2 H); 4.03-3.93 (m, 2 H); 3.93-3.81 (m, 2 H); 1.96-1.79 (m, 4 H).
Step 2; 4-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin5-yl)ethyl)amino)butyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate (compound 33B) The title compound was prepared as described in Example 54 Steps 5 to 6 with 3-(1,3-dioxolanyl)propyl 4-((3-(azido(phenyl)methyl)phenoxy)- methyl)benzoate replacing 4-((3-(azido(phenyl)methyl)phenoxy)methyl)-N- (4,4-diethoxybutyl)benzamide in Step 5 and the product used in subsequent steps. 115 The following compounds were prepared using the appropriate bromides in Example 55, Step 1 Compound Bromide x 34B 2-(4-bromobutyl)-1,3-dioxolane 2 35B 2-(5-bromopentyl)-1,3-dioxolane 3 4C 2-(6-bromohexyl)-1,3-dioxolane 4 The following compounds were prepared by coupling 4-((3- (azido(phenyl)methyl)phenoxy)methyl)benzoic acid (Example 51 Step 3) with the appropriate alcohol using the protocol below and the product so formed used in the subsequent steps for the preparation of Example 51.
To a stirred solution of the 4-((3- (azido(phenyl)methyl)phenoxy)methyl)benzoic acid and the appropriate alcohol (2.0 equivalents) in DMF (0.2 M) was added diisopropylethylamine (1.5 equivalents) and HATU (1.2 equivalents). The reaction mixture was heated at 60°C for 24 hours. The reaction mixture was diluted with ethyl acetate and was washed sequentially with aqueous 1M sodium hydroxide, water and brine. The organic phase was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude residue was purified by silica gel column chromatography eluting with 0-50% ethyl acetate in iso-hexane to afford the required compound. 116 Compound LINKER Appropriate alcohol 5C 6C 7C 8C Example 56 (3R)((((3-((4-(1-((4-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)butoxy)carbonyl)cyclopropyl)benzyl)- oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)(2-oxo phenylethyl)quinuclidinium (compound 36B) Step 1; Methyl 1-(p-tolyl)cyclopropanecarboxylate To a stirred solution of 1-(p-tolyl)cyclopropanecarboxylic acid (6 g, 117 34.05 mmol) in methanol (48 mL) was added para-toluenesulphonic acid monohydrate (0.648 g, 3.405 mmol). The reaction was stirred at 75°C for 16 hours. The mixture was concentrated under reduced pressure and the residue partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution. The organic layer was washed with saturated aqueous sodium bicarbonate solution (x 2), brine and dried (magnesium sulfate), filtered and concentrated under reduced pressure to afford the title compound as an orange oil (6.279 g, 97%). The material was used directly in the next step with no further purification.
¹H NMR (400 MHz, CDCl3): δ 7.25-7.21 (m, 2 H); 7.14-7.10 (m, 2 H); 3.62 (s, 3 H); 2.34 (s, 3 H); 1.60-1.56 (m, 2 H); 1.18-1.14 (m, 2 H).
Step2; Methyl 1-(4-(bromomethyl)phenyl)cyclopropanecarboxylate To a stirred solution of methyl 1-(p-tolyl)cyclopropanecarboxylate (3 g, .77 mmol) in acetonitrile (42 mL) was added N-bromosuccinimide (2.807 g, .77 mmol) followed by benzoyl peroxide (0.164 g, 0.473 mmol). The reaction was stirred at 80°C for 2 hours 40 minutes and then allowed to cool to room temperature. The reaction mixture was diluted with water and extracted with dichloromethane (x 3). The combined organic extracts were washed with brine and dried (magnesium sulfate), filtered and concentrated under reduced pressure to afford a red oil. The crude material was purified by silica gel column chromatography eluting with 0-9% ethyl acetate in iso-hexane to afford the title compound (2.478 g, 58%).
¹H NMR (400 MHz, CDCl3): δ 7.36-7.30 (m, 4 H); 4.49 (s, 2 H); 3.62 (s, 3 H); 1.63-1.59 (m, 2 H); 1.20-1.16 (m, 2 H). 118 Step 3; Methyl 1-(4-((3-benzoylphenoxy)methyl)- phenyl)cyclopropanecarboxylate Methyl 1-(4-(bromomethyl)phenyl)cyclopropanecarboxylate (2.478 g, 9.207 mmol) was added to a mixture of 3-hydroxybenzophenone (2.19 g, 11.05 mmol) and potassium carbonate (3.054 g, 22.10 mmol) in dimethyl formamide (46 mL). The reaction mixture was stirred at 60°C for 16 hours.
The reaction mixture was diluted with water and extracted with ethyl acetate (x 3). The combined organic extracts were washed with 10% aqueous potassium carbonate (x 5), 2M NaOH (x 5), brine and dried (magnesium sulfate), filtered and concentrated under reduced pressure to afford the title compound (3.721 g, quantitative yield). The material was used directly in the next step with no further purification.
¹H NMR (400 MHz, CDCl3): δ 7.81-7.77 (m, 2 H); 7.61-7.56 (m, 1 H); 7.50-7.35 (m, 9 H); 7.23-7.19 (m, 1 H); 5.10 (s, 2 H); 3.62 (s, 3 H); 1.64-1.59 (m, 2 H); 1.22-1.17 (m, 2 H).
Step 4; Methyl 1-(4-((3-(hydroxy(phenyl)methyl)phenoxy)- methyl)phenyl)cyclopropanecarboxylate To a stirred solution of methyl 1-(4-((3- benzoylphenoxy)methyl)phenyl)cyclopropanecarboxylate (1.85 g, 4.787 mmol) in methanol (22.6 mL) at 0°C under an atmosphere of nitrogen was added sodium borohydride (0.181 g, 4.787 mmol) in one portion. The reaction mixture was stirred at 0 ºC for 1 hour and then allowed to warm to 119 room temperature. After stirring for 40 minutes the reaction was cooled to 0 ºC and additional sodium borohydride (0.091 g, 2.380 mmol) was added. The reaction mixture was allowed to warm to room temperature and stirred for 30 minutes. The reaction was quenched with water (3.5 mL), filtered to remove insoluble material and then concentrated under reduced pressure. Water was added to the residue and extracted with ethyl acetate (x 2). The combined organic extracts were washed with 10% aqueous potassium carbonate (x 2), brine, dried (magnesium sulfate), filtered and concentrated under reduced pressure to afford the title compound as a red oil (1.824 g, 98%). The material was used directly in the next step with no further purification.
¹H NMR (400 MHz, CDCl3): δ 7.40-7.22 (m, 10 H); 7.05-7.03 (m, 1 H); 6.98 (d, J = 7.7 Hz, 1 H); 6.87 (dd, J = 8.3, 2.6 Hz, 1 H); 5.82 (d, J = 3.4 Hz, 1 H); 5.02 (s, 2 H); 3.62 (s, 3 H); 2.20 (d, J = 3.6 Hz, 1 H); 1.63-1.59 (m, 2 H); 1.20-1.16 (m, 2 H).
Step 5; Methyl 1-(4-((3-(azido(phenyl)methyl)phenoxy)methyl)- phenyl)cyclopropanecarboxylate To a stirred solution of methyl 1-(4-((3-(hydroxy(phenyl)methyl)- phenoxy)methyl)phenyl)cyclopropanecarboxylate (1.824 g, 4.695 mmol) in toluene (21.8 mL) under an atmosphere of nitrogen was added diphenylphosphoryl azide (1.21 mL, 5.635 mmol) followed by 1,8-diazabicyclo[5.4.0]undecene (0.84 mL, 5.635 mmol). The reaction mixture was stirred at 100°C for 3 hours and then allowed to cool to room temperature. The reaction was quenched by addition of saturated aqueous ammonium chloride solution and extracted with ethyl acetate (x 3). The combined organic extracts were washed with brine and dried (magnesium 120 sulfate), filtered and concentrated under reduced pressure to afford a brown oil. The crude material was purified by silica gel chromatography eluting with 0-14% ethyl acetate in iso-hexane to afford the title compound as a colourless oil (1.214 g, 62%).
¹H NMR (400 MHz, CDCl3): δ 7.38-7.25 (m, 10 H); 6.95-6.89 (m, 3 H); .67 (s, 1 H); 5.01 (s, 2 H); 3.62 (s, 3 H); 1.63-1.59 (m, 2 H); 1.20-1.16 (m, 2 H).
Step 6; 1-(4-((3-(Azido(phenyl)methyl)phenoxy)methyl)phenyl)- cyclopropanecarboxylic acid To a stirred solution of methyl 1-(4-((3-(azido(phenyl)methyl)- phenoxy)methyl)phenyl)cyclopropanecarboxylate (0.569 g, 1.375 mmol) in methanol (12.9 mL) and tetrahydrofuran (5.1 mL) was added 2M aqueous sodium hydroxide (12.9 mL). The reaction was stirred at 50°C for 3 hours 30 minutes and then at room temperature for 16 hours. The reaction mixture was concentrated under reduced pressure and the pH adjusted to pH4 using 2M aqueous hydrochloric acid with stirring. The mixture was extracted with dichloromethane (x 3) and the combined organic extracts washed with brine, dried (magnesium sulfate), filtered and concentrated under reduced pressure to afford the title compound (0.552 g, quantitative yield). The material was used directly in the next step with no further purification ¹H NMR (400 MHz, CDCl3): δ 7.39-7.24 (m, 10 H); 6.94-6.88 (m, 3 H); .67 (s, 1 H); 5.00 (s, 2 H); 1.69-1.65 (m, 2 H); 1.28-1.24 (m, 2 H).
Step 7; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin5-yl)ethyl)amino)butyl 1-(4-((3-(phenyl((((R)-quinuclidinyloxy)- 121 carbonyl)amino)methyl)phenoxy)methyl)phenyl)cyclopropanecarboxylate N H O OH HO N H O NH O N O O O The title compound was prepared as described in Example 54 Step 1 through 2 with 1-(4-((3-(Azido(phenyl)methyl)phenoxy)methyl)phenyl)- cyclopropanecarboxylic acid replacing 4-((3-(azido(phenyl)methyl)- phenoxy)methyl)benzoic acid in Step 1 and the product used in the subsequent steps.
Step 8; (3R)((((3-((4-(1-((4-(((R)hydroxy(8-hydroxyoxo10 1,2-dihydroquinolinyl)ethyl)amino)butoxy)carbonyl)cyclopropyl)- benzyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)(2-oxo phenylethyl)quinuclidinium (compound 36B) The title compound was prepared as in Example 24 with 4-(((R) hydroxy(8-hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)butyl 1-(4-((3-(phenyl((((R)-quinuclidinyloxy)carbonyl)amino)methyl)- phenoxy)methyl)phenyl)cyclopropanecarboxylate replacing (R)- quinuclidinyl (3-(6-((R)hydroxy(8-hydroxyoxo-1,2- 122 dihydroquinolinyl)ethylamino)hexyloxy)phenyl)(phenyl)- methylcarbamate.
Example 57 (R)-quinuclidinyl ((3-(2-(4'-((((R)hydroxy(8-hydroxyoxo5 1,2-dihydroquinolinyl)ethyl)amino)methyl)-[1,1'-biphenyl] yl)ethoxy)phenyl)(phenyl)methyl)carbamate (compound 37B) Step 1; tert-Butyl ((3-(4-bromophenethoxy)- phenyl)(phenyl)methyl)carbamate The title compound was prepared as described in Example 22 Step 2 with 4-bromophenethyl alcohol and tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate replacing (4-((1,3-dioxolan yl)methyl)phenyl)methanol and 3-hydroxybenzophenone respectively.
¹H NMR (400 MHz, CDCl3): δ 7.44-7.39 (m, 2 H); 7.34-7.18 (m, 6 H); 7.16-7.11 (m, 2 H); 6.84-6.74 (m, 3 H); 5.86 (s, 1 H); 5.12 (s, 1 H); 4.15-4.08 (m, 2 H); 3.01 (t, J = 6.8 Hz, 2 H); 1.43 (s, 9 H).
Step 2; (3-(4-bromophenethoxy)phenyl)(phenyl)methanamine hydrochloride 123 The title compound was prepared as described in Example 50 Step 4 with tert-butyl ((3-(4-bromophenethoxy)phenyl)(phenyl)methyl)carbamate replacing tert-butyl ((3-((4'-((1,3-dioxolanyl)methyl)-[1,1'-biphenyl] yl)methoxy)phenyl)(phenyl)methyl)carbamate ¹H NMR (400 MHz, DMSO-d6): δ 8.95 (s, 3 H); 7.53-7.27 (m, 10 H); 7.14-7.10 (m, 1 H); 7.05-7.00 (m, 1 H); 6.96-6.90 (m, 1 H); 5.61-5.54 (m, 1 H); 4.18 (t, J = 6.7 Hz, 2 H); 3.02 (t, J = 6.7 Hz, 2 H).
Step 3; (R)-quinuclidinyl ((3-(4-bromophenethoxy)phenyl)- (phenyl)methyl)carbamate The title compound was prepared as described in Example 1 Step 5 with (3-(4-bromophenethoxy)phenyl)(phenyl)methanamine hydrochloride replacing (3-(8-(1,3-dioxolanyl)octyloxy)phenyl)(phenyl)methanamine ¹H NMR (400 MHz, CDCl3): δ 7.45-7.39 (m, 2 H); 7.37-7.19 (m, 6 H); 7.16-7.10 (m, 2 H); 6.87-6.75 (m, 3 H); 5.90 (s, 1 H); 5.29 (s, 1 H); 4.75-4.68 (m, 1 H); 4.16-4.07 (m, 2 H); 3.26-3.13 (m, 1 H); 3.01 (t, J = 6.8 Hz, 2 H); 2.93-2.62 (m, 5 H); 2.02-1.96 (m, 1 H); 1.86-1.75 (m, 1 H); 1.71-1.44 (m, 2 H); 1.42-1.29 (m, 1 H).
Step 4; (R)-quinuclidinyl ((3-(2-(4'-formyl-[1,1'-biphenyl] yl)ethoxy)phenyl)(phenyl)methyl)carbamate (R)-quinuclidinyl ((3-(4-bromophenethoxy)phenyl)(phenyl)methyl)- 124 carbamate (0.40 g, 0.747 mmol), 4-formylphenylboronic acid (0.123 g, 0.822 mmol), sodium carbonate (0.158 g, 1.494 mmol) were combined in toluene (9.94 mL) and water (2.48 mL). The mixture was degassed with nitrogen for 10 minutes. Tetrakis(triphenylphosphine)palladium(0) (0.087 g, 0.075 mmol) was added and the mixture heated at 120°C for 30 minutes in a microwave. The mixture was filtered and the filtrate partitioned between ethyl acetate and water. The organic layer was dried (sodium sulfate), filtered and concentrated under reduced pressure to afford a brown oil. The crude material was partially purified using a flash C18 cartridge eluting with 30-60% acetonitrile in water to afford a brown oil (0.174 g). The material was used directly in the next step with no further purification.
Step 5; (R)-quinuclidinyl ((3-(2-(4'-((((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)methyl)-[1,1'- biphenyl]yl)ethoxy)phenyl)(phenyl)methyl)carbamate The title compound was prepared as described in Example 1 Step 7 with (R)-quinuclidinyl ((3-(2-(4'-formyl-[1,1'-biphenyl] yl)ethoxy)phenyl)(phenyl)methyl)carbamate replacing (R)-quinuclidinyl (3-(9-oxononyloxy)phenyl)(phenyl)methylcarbamate. 125 Example 58 (R)-quinuclidinyl (3-(2-(3'-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethylamino)methyl)biphenyl yl)ethoxy)phenyl)(phenyl)methylcarbamate (compound 38B) The title compound was prepared as described in Example 57 with 3- formylboronic acid replacing 4-formylboronic acid in Step 4 and the product used in the subsequent step.
Example 59 6-((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyl 2-(3-(phenyl(((R)-quinuclidinyloxy)- carbonylamino)methyl)phenoxy)acetate (compound 39B) Step 1; Methyl 2-(3-(((tert-butoxycarbonyl)amino)- (phenyl)methyl)phenoxy)acetate The title compound was prepared as described in Example 1 Step 1 with tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate and methyl bromoacetate replacing 3-hydroxybenzophenone and 2-(8-bromooctyl)-1,3- dioxolane respectively Step 2; 2-(3-(((tert-Butoxycarbonyl)amino)(phenyl)- 126 methyl)phenoxy)acetic acid The title compound was prepared as described in Example 56 Step 6 with methyl 2-(3-(((tert-butoxycarbonyl)amino)(phenyl)methyl)- phenoxy)acetate replacing methyl 1-(4-((3-(azido(phenyl)methyl)phenoxy)- methyl)phenyl)cyclopropanecarboxylate.
Step 3; 5-(1,3-Dioxolanyl)pentyl 2-(3-(((tertbutoxycarbonyl)amino)(phenyl)methyl)phenoxy)acetate The title compound was prepared as described in Example 54 Step 1 with -(3-(((tert-Butoxycarbonyl)amino)(phenyl)methyl)phenoxy)acetic acid and 2-(5-bromopentyl)-1,3-dioxolane 4-((3-(azido(phenyl)methyl)phenoxy)- methyl)benzoic acid and 2-(3-chloropropyl)-1,3-dioxolane respectively.
Step 4; 6-((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyl 2-(3-(phenyl(((R)-quinuclidinyloxy)- carbonylamino)methyl)phenoxy)acetate (compound 40B) The title compound was prepared as described in Example 53 Step 3 and Step 4 with 5-(1,3-dioxolanyl)pentyl 2-(3-(((tert-butoxycarbonyl)- amino)(phenyl)methyl)phenoxy)acetate replacing tert-butyl ((3-((4'-((1,3- dioxolanyl)methyl)-[1,1'-biphenyl]yl)methoxy)phenyl)(phenyl)- methyl)carbamate in Step 3 and the product used in the subsequent steps.
The following compounds were prepared using the appropriate alkylating agent in Example 59 Step 1 and the appropriate coupling partner 127 replacing 2-(5-bromopentyl)-1,3-dioxolane in Example 59 Step 3; N H N H O OH HO LINK O R R O NH O O N n Cpd. LINK Coupling partner Alkylatin g agent n R 9C pentyl 0 H 10C butyl 0 H 11C pentyl 0 Me 12C butyl 0 Me 13C pentyl 1 Me 14C 0 H 15C 0 H The coupling partner for Compound 14C was prepared from 1-(tert5 butoxycarbonyl)piperidinecarboxylic acid and 2-(3-bromopropyl)-1,3- dioxolane using standard alkylation conditions detailed in Example 1 Step 1.
Example 60 (R)-Quinuclidinyl ((3-((9-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy) methylphenyl)(phenyl)methyl)carbamate (Compound 16C) The title compound was prepared as described in Example 35. 128 Example 61 (R)-Quinuclidinyl ((3-bromo((9-(((R)hydroxy(8-hydroxy2-oxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)- (phenyl)methyl)carbamate (Compound 17C) The title compound was prepared as described in Example 28.
Example 62 (R)-Quinuclidinyl ((5-((9-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)-[1,1'-biphenyl] yl)(phenyl)methyl)carbamate (Compound 18C) The title compound was prepared as described in Example 40.
Example 63 (R)-Quinuclidinyl ((2-bromo((9-(((R)hydroxy(8-hydroxy2-oxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)- (phenyl)methyl)carbamate (Compound 19C) The title compound was prepared as described in Example 29 with 2- bromohydroxybenzaldehyde used in Step 1.
Example 64 (R)-Quinuclidinyl ((3'-fluoro((9-(((R)hydroxy(8-hydroxy- 129 2-oxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)-[1,1'-biphenyl] yl)(phenyl)methyl)carbamate (Compound 20C) The title compound was prepared as described in Example 40 with 3- fluorophenylboronic acid replacing phenyl boronic acid in Step 1.
Example 65 (R)-Quinuclidinyl ((3-((3-(4-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)butoxy)benzyl)oxy)phenyl)- (phenyl)methyl)carbamate (Compound 21C) The title compound was prepared as described in Example 42 Step 2 Example 66 (R)-Quinuclidinyl ((3-((3-((5-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)pentyl)oxy)benzyl)oxy)- phenyl)(phenyl)methyl)carbamate (Compound 22C) The title compound was prepared as described in Example 44.
Example 67 (3R)(((Cyclohexyl(3-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)methyl)carbamoyl)- 130 oxy)(2-oxophenylethyl)quinuclidinium (Compound 23C) The title compound was prepared as described in Example 24 with Compound 1C replacing (R)-quinuclidinyl (3-(6-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)hexyloxy)- phenyl)(phenyl)methylcarbamate Example 68 (3R)((((3-((6-(((R)Hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(thiophen yl)methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (Compound 24C) HN O HO OH HN O H N O N + O O S The title compound was prepared as described in Example 24 with Compound 2C replacing (R)-quinuclidinyl (3-(6-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)hexyloxy)phenyl)- (phenyl)methylcarbamate.
Example 69 (3R)((((3-Fluorophenyl)(3-((6-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)methyl)- carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (Compound 25C) 131 The title compound was prepared as described in Example 24 with Compound 24B replacing (R)-quinuclidinyl (3-(6-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)hexyloxy)phenyl)- (phenyl)methylcarbamate.
Example 70 (3R)((((3-((6-(((R)Hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(thiophen yl)methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (Compound 26C) The title compound was prepared as described in Example 24 with Compound 3C replacing (R)-quinuclidinyl (3-(6-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)- hexyloxy)phenyl)(phenyl)methylcarbamate.
Example 71 (3R)((((3-((4-((4-(((R)Hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)butyl)carbamoyl)benzyl)oxy)phenyl)- (phenyl)methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (Compound 27C) The title compound was prepared as described in Example 24 with Compound 31B replacing (R)-quinuclidinyl (3-(6-((R)hydroxy(8- 132 hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyloxy)phenyl)(phenyl)methylcarbamate.
Example 72 (3R)((((3-((7-(((R)Hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)heptyl)oxy)phenyl)(phenyl)methyl)- carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (Compound 28C) The title compound was prepared as described in Example 24 with Compound 3 replacing (R)-quinuclidinyl (3-(6-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)hexyloxy)phenyl)- (phenyl)methylcarbamate.
Example73 (3R)((((3-((7-(((R)Hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)heptyl)oxy)phenyl)(phenyl)methyl)- carbamoyl)oxy)(3-phenylpropyl)quinuclidinium (Compound 29C) N H O OH HO N H O HN O O N + The title compound was prepared as described in Example 24 with Compound 3 replacing (R)-quinuclidinyl (3-(6-((R)hydroxy(8- 133 hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)hexyloxy)phenyl)- (phenyl)methylcarbamate and (3-bromopropyl)benzene replacing bromoacetophenone.
Example 74 (3R)((((3-((5-(((R)Hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)pentyl)oxy)phenyl)(phenyl)methyl)- carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (Compound 30C) The title compound was prepared as described in Example 24 with Compound 5 replacing (R)-quinuclidinyl (3-(6-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyloxy)phenyl)(phenyl)methylcarbamate.
Example 75 4-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 1-(4-((3-(phenyl((((R)-quinuclidinyloxy)carbonyl)- amino)methyl)phenoxy)methyl)phenyl)cyclopentanecarboxylate (Compound 31C) The title compound was prepared as described in Example 56 Step1 through Step 7 with 1-(p-tolyl)cyclopentanecarboxylic acid replacing 134 1-(p-tolyl)cyclopropanecarboxylic acid in Step 1.
Example 76 4-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 1-(4-((3-(phenyl((((R)-quinuclidinyloxy)carbonyl)- amino)methyl)phenoxy)methyl)phenyl)cyclohexanecarboxylate (Compound 32C) The title compound was prepared as described in Example 56 Step1 through Step 7 with 1-(p-tolyl)cyclohexanecarboxylic acid replacing 1-(p10 tolyl)cyclopropanecarboxylic acid in Step 1.
Example 77 4-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-methyl(4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)phenyl)propanoate (Compound 33C) The title compound was prepared as described in Example 56 Step1 through Step 7 with 2-methyl(p-tolyl)propanoic acid replacing 1-(p-tolyl)cyclopropanecarboxylic acid in Step 1. 135 Synthesis of benzoic acid derivatives: Example 78 8-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)octyl 3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzoate (Compound 34C) Step 1; Methyl 3-benzoylbenzoate A stirred solution of 3-benzoylbenzoic acid (10.0 g, 44.4 mmol) and p-TSA (0.85 g, 4.39 mmol) in methanol (200 mL) was heated at 75°C for 18 hours. The reaction mixture was allowed to cool and the solvent evaporated at reduced pressure. The residue was partitioned between ethyl acetate and saturated aqueous sodium hydrogen carbonate. The organic phase was dried with anhydrous sodium sulfate, filtered and the filtrate evaporated at reduced pressure to afford the title compound (9.55 g, 90%).
¹H NMR (400 MHz, CDCl3): δ 8.44 (s, 1H); 8.27 (m, 1 H); 8.01 (m, 1 H); 7.86 (m 2 H); 7.61 (m, 2 H); 7.50 (m, 2 H); 3.94 (s, 3 H). 136 Step 2; Methyl 3-(hydroxy(phenyl)methyl)benzoate The title compound was prepared as described in Example 1 Step 2 with methyl 3-benzoylbenzoate replacing (3-(8-(1,3-dioxolan yl)octyloxy)phenyl)(phenyl)methanone.
¹H NMR (400 MHz, CDCl3): δ 8.07 (s, 1 H); 7.90 (m, 2 H); 7.58 (m, 1 H); 7.40-7.21 (m, 6 H); 5.87 (s, 1 H); 3.88 (s, 3 H); 2.46 (s, 1 H).
Step 3; Methyl 3-(azido(phenyl)methyl)benzoate The title compound was prepared as described in Example 1 Step 3 with methyl 3-(hydroxy(phenyl)methyl)benzoate replacing (3-(8-(1,3- dioxolanyl)octyloxy)phenyl)(phenyl)methanol.
¹H NMR (400 MHz, CDCl3): δ 8.09 (s, 1 H); 7.99 (m, 1 H); 7.50-7.20 (m, 7 H); 5.75 (s, 1 H); 3.93 (s, 3 H).
Step 4; 3-(Azido(phenyl)methyl)benzoic acid The title compound was prepared as described in Example 56 Step 6 with methyl 3-(azido(phenyl)methyl)benzoate replacing methyl 1-(4-((3- (azido(phenyl)methyl)phenoxy)methyl)phenyl)cyclopropanecarboxylate.
¹H NMR (400 MHz, CDCl3): δ 8.15 (s, 1 H); 8.00 (m, 1 H); 7.56 (m, 1 H); 7.47 (m, 1 H), 7.40-7.20 (m, 5 H); 5.72 (s, 1 H).
Step 5; 7-(1,3-Dioxolanyl)heptyl 3-(azido(phenyl)methyl)benzoate 137 The title compound was prepared as described in Example 54 Step 1 with 3-(7-bromoheptyl)-1,3-dioxolane and 3-(azido(phenyl)methyl)benzoic acid replacing 2-(3-chloropropyl)-1,3-dioxolane and 4-((3- (azido(phenyl)methyl)phenoxy)methyl)benzoic acid respectively.
Step 6; 8-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin5-yl)ethyl)amino)octyl 3-(phenyl((((R)-quinuclidinyloxy)carbonyl)- amino)methyl)benzoate (Compound 34C) The title compound was prepared as described in Example 54 Step 2.
The following compounds were prepared using the appropriate alkylating agent in Example 80 Step 5 and using the products in the subsequent steps.
Alcohol based alkylating agents were coupled using the conditions described in Example 22 Step 2 with the appropriate alcohol replacing (4-((1,3-dioxolan yl)methyl)phenyl)methanol. Amine based alkylating agents were coupled using the conditions described in Example 51 Step 4 with the appropriate amine replacing 4-amino-butyraldehyde diethyl ether.
Compound Linker Alkylating agent 35C 36C 37C 38C (continued) 138 39C 40C 41C 42C Example 79 (2S)(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 3-phenyl(4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzamido)propanoate (Compound 43C) Step 1; Step 1; N-((3-hydroxyphenyl)(phenyl)methyl)formamide 3-Hydroxybenzophenone (25 g, 126.1 mmol) in formamide (130 mL, 3.3 mmol) was heated to 180°C for 18 hours. The reaction was allowed to cool slightly then poured into ice-cooled water and stirred for 30 minutes, filtered and washed with water. The solid was stirred in water (60 mL) and ethanol (60 mL) and heated to 50 ºC for 1 hour, then allowed to cool. The solid was filtered and washed with water to give the title compound (33.94 g, 118%).
¹H NMR (400 MHz, CD3OD): δ 7.39-7.28 (m, 5 H); 7.21-7.13 (m, 1 H); 139 6.79 (d, J = 7.78 Hz, 1 H); 6.73-6.68 (m, 2 H); 5.45 (s, 1 H).
Step 2; 3-(Amino(phenyl)methyl)phenol hydrochloride Methanol (125 mL), was cooled to 0°C and acetyl chloride (17.8 mL) added dropwise to give a 2M solution of methanolic hydrogen chloride. N-((3- hydroxyphenyl)(phenyl)methyl)formamide was stirred at 40°C for 1.5 hours with the 2M methanolic hydrogen chloride. The solvent was removed under reduced pressure and the residue re-dissolved in methanol and the solvent removed under reduced pressure. This process was repeated three times to give the title compound (29.09 g, 97.9%).
¹H NMR (400 MHz, DMSO-d6): δ 9.76 (s, 1 H); 9.07 (s, 3 H); 7.59-7.53 (m, 2 H); 7.51-7.37 (m, 3 H); 7.26 (t, J = 7.89 Hz, 1 H); 6.99 (d, J = 7.75 Hz, 1 H); 6.90 (t, J = 1.97 Hz, 1 H); 6.81 (dd, J = 8.10, 2.32 Hz, 1 H); 5.58 (d, J = .82 Hz, 1 H).
Step 3; tert-Butyl (3-hydroxyphenyl)(phenyl)methylcarbamate 3-(Amino(phenyl)methyl)phenol hydrochloride (29.09 g, 123.4 mmol) in dichloromethane (450 mL) was cooled to 0°C and diisopropylethylamine (65.9 mL, 370.2 mmol) and di-tert-butyl dicarbonate (59.2 g, 271.5 mmol) was added slowly. The reaction was stirred at 0°C for 2 hours then warmed to room temperature over 16 hours. The solvent was removed and compound purified through a silica plug, eluting with 0-20% ethyl acetate in iso-hexane to give a black oil. To this mixture in methanol (300 mL) was added potassium carbonate (51 g, 370.2 mmol) and stirred at 140 room temperature for 16 hours. The suspension was filtered and the filtrate was evaporated at reduced pressure and the residue re-dissolved in ethyl acetate (370 mL). Silica (73 g) was added and the suspension was stirred for minutes, filtered, and the filter cake washed with further ethyl acetate. The filtrate was evaporated to dryness. The dark solid residue was dissolved in ethyl acetate (200 m L) was charcoal added and the suspension was heated under refluxed for 1 hour. The suspension was filtered through celite and solvent removed at reduced pressure. The dark solid was dissolved in dichloromethane and iso-hexane added then solvent evaporated (repeated 3 times) to give the title compound (34.81 g, 92%).
¹H NMR (400 MHz, CDCl3): δ 7.36-7.16 (m, 6 H); 6.80 (d, J = 7.79 Hz, 1 H); 6.74-6.69 (m, 2 H); 5.83 (s, 1 H); 5.15 (s, 1 H); 1.53-1.30 (s, 9 H).
Step 4; Methyl 4-((3-(((tertbutoxycarbonyl)amino)(phenyl)methyl)phenoxy)methyl)benzoate A mixture of tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate (3.20 g, 10.7 mmol), methyl 4-(bromomethyl)benzoate (2.70 g, 11.8 mmol) and potassium carbonate (2.20 g, 16.1 mmol) in acetonitrile (54 mL) was stirred at room temperature for 16 hours. The reaction mixture was concentrated at reduced pressure and the residue partitioned between ethyl acetate and water. The aqueous phase was extracted with further ethyl acetate and the combined organic extracts combined, dried with anhydrous magnesium sulfate, filtered and the solvent evaporated at reduced pressure.
The residue was re-crystallised from ethyl acetate and iso-hexane to afford the 141 title compound (3.25 g, 68%).
¹H NMR (400 MHz, CDCl3): δ 8.04 (d, J = 8.2 Hz, 2 H); 7.46 (d, J = 8.2 Hz, 2 H); 7.34-7.20 (m, 6 H); 6.90-6.81 (m, 3 H); 5.87 (s, 1 H); 5.13 (s, 1 H); 5.07 (s, 2 H); 3.92 (s, 3 H); 1.44 (s, 9 H).
Step 5; Methyl 4-((3-(amino(phenyl)methyl)phenoxy)- methyl)benzoate hydrochloride To a solution of methyl 4-((3-(((tert-butoxycarbonyl)amino)- (phenyl)methyl)phenoxy)methyl)benzoate (3.21 g, 7.20 mmol) in methanol (36 mL) was added hydrogen chloride in dioxane (4 M, 9.0 mL, 36 mmol).
The reaction mixture was stirred at room temperature for 16 hours. The solvent was removed at reduced pressure to afford the title compound (2.65 g, >95%).
¹H NMR (400 MHz, CDCl3): δ 9.21 (s, 2 H); 8.03 (d, J = 8.1 Hz, 2 H); 7.64 (d, J = 8.1 Hz, 2 H); 7.59 (d, J = 7.6 Hz, 2 H); 7.49-7.34 (m, 5 H); 7.17 (d, J = 7.7 Hz, 1 H); 7.06 (dd, J = 8.3, 2.4 Hz, 1 H); 5.64 (s, 1 H); 5.28 (s, 2 H); 3.91 (s, 3 H).
Step 6; Methyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate The title compound was prepared as in Example 1 Step 5 with methyl 4-((3-(amino(phenyl)methyl)phenoxy)methyl)benzoate hydrochloride replacing (3-(8-(1,3-dioxolanyl)octyloxy)phenyl)(phenyl)methanamine. 142 Step 7; 4-((3-(Phenyl((((R)-quinuclidinyloxy)carbonyl)amino)- methyl)phenoxy)methyl)benzoic acid To a stirred solution of methyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate (2.27 g, 4.50 mmol) in THF (23 mL) was added an aqueous solution of lithium hydroxide (2.0 M, 9.0 ml, 18.0 mmol). The mixture was stirred at room temperature for 16 hours. The pH of the reaction mixture was adjusted to 6 by the addition of 4M aqueous hydrochloric acid. The mixture was then extracted with 10% methanolic ethyl acetate (x2) and the combined organic extracts evaporated at reduced pressure. The residue was then dissolved in ethanol and re-evaporated at reduced pressure to afford the title compound (1.85 g, 84%).
¹H NMR (400 MHz, DMSO-d6): δ 8.41 (d, J = 9.4 Hz, 1 H); 7.99 (d, J = 7.9 Hz, 2 H); 7.58 (d, J = 8.0 Hz, 2 H); 7.42-7.26 (m, 6 H); 7.09 (s, 1 H); 7.02- 6.91 (m, 2 H); 5.87 (d, J = 9 Hz, 1 H); 5.21 (s, 2 H); 4.76 (s, 1 H); 3.98-2.72 (m, 6 H); 2.12-1.54 (m, 5 H).
Step 8; (S)(1,3-Dioxolanyl)propyl 2-amino phenylpropanoate The title compound was prepared in two steps. Boc-Phe-OH was reacted with 2-(3-chloropropyl)-1,3-dioxolane according to Example 10 Step 1 and the subsequent product reacted with hydrogen chloride in dioxane according to Example 79 Step 5.
Step 9; 2S)(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)butyl 3-phenyl(4-((3-(phenyl((((R)- 143 quinuclidinyloxy)carbonyl)amino)methyl)phenoxy)methyl)- benzamido)propanoate (Compound 43C) The title compound was prepared in three steps. The product from Example 79 Step 7 was coupled to the product from Example 79 Step 8 using the method described in Example 51 Step 4. The subsequent product was then used in the methods of Example 1 Step 6 followed by Example 1 Step 7.
Example 80 (R)-Quinuclidinyl ((3-((3-(4-(2-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)ethyl)phenyl)-1,2,4-oxadiazol yl)methoxy)phenyl)(phenyl)methyl)carbamate (Compound 44C) Step 1; 4-((1,3-Dioxolanyl)methyl)benzonitrile To a stirred solution of 4-(2-hydroxyethyl)benzonitrile (1.09 g, 7.41 mmol) in DCM (20 mL) was added Dess-Martin Periodinane (3.77 g, 8.84 mmol) and the reaction mixture stirred at room temperature for 1 hour. A 1:1 mixture of saturated aqueous sodium hydrogen carbonate and saturated sodium thiosulfate was added and the bi-phasic mixture stirred for 1 hour. The organic phase was separated and the aqueous phase extracted with further 144 DCM (x3). The combined organic extracts were dried with anhydrous magnesium sulfate and the solvent evaporated at reduced pressure. The crude material was dissolved in toluene (40 mL) and ethylene glycol (2.29 g, 37.05 mmol) and p-toluenesulfonic acid (0.14 g, 0.74 mmol) added. The mixture was heated under Dean and Stark conditions for 2 hours. The solvent was evaporated under reduced pressure and the residue partitioned between saturated aqueous sodium hydrogen carbonate and ethyl acetate. The organic phase was removed and the aqueous phase was extracted with further ethyl acetate (x3). The combined organic phases were dried with anhydrous magnesium sulfate and the solvent evaporated at reduced pressure to afford the title compound (1.40 g, 99%).
¹H NMR (400 MHz, CDCl3): δ 7.69-7.53 (m, 2 H); 7.48-7.34 (m, 2 H); .08 (t, J = 4.5 Hz, 1 H); 3.94-3.81 (m, 4 H); 3.03 (t, J = 4.5 Hz, 2 H).
Step 2; 4-((1,3-Dioxolanyl)methyl)-N'-hydroxybenzimidamide To a solution of 4-((1,3-dioxolanyl)methyl)benzonitrile (1.40 g, 7.41 mmol) in ethanol (10 mL) was added 50% aqueous hydroxylamine (5 mL) and the resultant mixture heated at 80°C for 16 hours. The solvent was evaporated at reduced pressure and the residue partitioned between ethyl acetate and brine. The organic phase was removed and the aqueous phase was extracted with further ethyl acetate (x2). The combined organic extracts were dried with aqueous magnesium sulfate and evaporated at reduced pressure to afford the title compound (1.21 g, 73%).
¹H NMR (400 MHz, DMSO-d6): δ 9.57 (s, 1 H); 7.62-7.49 (m, 2 H); 7.34-7.23 (m, 2 H); 5.76 (s, 2 H); 5.03-4.90 (m, 1 H); 3.95-3.66 (m, 4 H); 2.91 (dd, J = 16.6, 4.9 Hz, 2 H).
Step 3, tert-butyl ((3-((3-(4-((1,3-Dioxolanyl)methyl)phenyl)- 145 1,2,4-oxadiazolyl)methoxy)phenyl)(phenyl)methyl)carbamate To a stirred solution of 4-((1,3-dioxolanyl)methyl)-N'- hydroxybenzimidamide (0.747 g, 3.35 mmol) and 2-(3-(((tert5 butoxycarbonyl)amino)(phenyl)methyl)phenoxy)acetic acid (Example 59 Step 2, 1.0 g, 2.79 mmol)) in acetonitrile (5 mL) was added 1-ethyl(3- dimethyllaminopropyl)carbodiimide hydrochloride (0.8 g, 4.18 mmol). The reaction mixture was stirred at ambient temperature for 16 hours. The reaction mixture was diluted with pyridine (1 mL) and heated at 150°C for 30 minutes in a microwave. The reaction was diluted with saturated brine and extracted with ethyl acetate (x3). The combined organic fractions were dried with magnesium sulfate and the solvent evaporated at reduced pressure. Material used directly in the next step without further purification (1.01 g, 65%).
¹H NMR (400 MHz, CDCl3): δ 8.04-7.96 (m, 2 H); 7.45-7.37 (m, 2 H); 6.96-6.88 (m, 3 H); 5.88 (s, 1 H); 5.29 (s, 2 H); 5.19-5.07 (m, 2 H); 3.98-3.80 (m, 4 H); 3.03 (d, J = 4.6 Hz, 2 H); 1.44 (s, 9 H).
Step 4; (3-((3-(4-(2,2-dimethoxyethyl)phenyl)-1,2,4-oxadiazol yl)methoxy)phenyl)(phenyl)methanamine Hydrogen chloride in dioxane (4.0 M, 5 mL, 24 mmol) was added to a solution of tert-butyl ((3-((3-(4-((1,3-dioxolanyl)methyl)phenyl)-1,2,4- oxadiazolyl)methoxy)phenyl)(phenyl)methyl)carbamate (1.01 g, 1.85 mmol) in methanol (5 mL) and the resultant solution was stirred at ambient temperature for 2 hours. The solvent was evaporated at reduced pressure and the residue loaded onto an SCX-2 cartridge. The cartridge was eluted with 146 methanol (eight column volumes) followed by ammonia/methanol. Fractions containing the product were combined and evaporated at reduced pressure to afford the title compound (0.796 g, 96%).
¹H NMR (400 MHz, CDCl3): δ 8.02 (d, J = 8.0 Hz, 2 H); 7.42-7.15 (m, 8 H); 7.12-7.01 (m, 2 H); 6.88 (dd, J = 8.2, 2.7 Hz, 1 H); 5.34-5.27 (m, 2 H); .19 (s, 1 H); 4.60-4.54 (m, 1 H); 3.38-3.31 (m, 6 H); 2.98 (d, J = 5.6 Hz, 2 H).
Step 5; (R)-quinuclidinyl ((3-((3-(4-(2-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)ethyl)phenyl)-1,2,4- oxadiazolyl)methoxy)phenyl)(phenyl)methyl)carbamate (Compound 44C) The title compound was prepared as described in Example 1 Step 5, 6 and 7.
Example 81 (R)-Quinuclidinyl ((5-((9-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)pyridin yl)(phenyl)methyl)carbamate (Compound 45C) The title compound was prepared as described in Example 10 with 5- hydroxynicotinaldehyde replacing 3-hydroxybenzaldehyde in Step 1 and phenyl magnesium bromide replacing 2-thienylmagnesium bromide in Step 2. 147 Example 82 (R)-Quinuclidinyl ((3-fluorophenyl)(5-((9-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)pyridin yl)methyl)carbamate (Compound 46C) The title compound was prepared as described in Example 10 with -hydroxynicotinaldehyde replacing 3-hydroxybenzaldehyde in Step 1 and 3-fluorophenyl magnesium bromide replacing 2-thienylmagnesium bromide in Step 2.
Synthesis of single diastereoisomers Chiral Example 1 (R)-Quinuclidinyl ((3-((6-(((R)hydroxy(8-hydroxyoxo15 1,2-dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(phenyl)- methyl)carbamate (compound 41B) 148 Step 1; N-((3-hydroxyphenyl)(phenyl)methyl)formamide 3-Hydroxybenzophenone (25 g, 126.1 mmol) in formamide (130 mL, 3.3 mmol) was heated to 180°C for 18 hours. The reaction was allowed to cool slightly then poured into ice-cooled water and stirred for 30 minutes, filtered and washed with water. The solid was stirred in water (60 mL) and ethanol (60 mL) and heated to 50 ºC for 1 hour, then allowed to cool. The solid was filtered and washed with water to give the title compound (33.94 g, 118%).
¹H NMR (400 MHz, CH3OH-d4): δ 7.39-7.28 (m, 5 H); 7.21-7.13 (m, 1 H); 6.79 (d, J = 7.78 Hz, 1 H); 6.73-6.68 (m, 2 H); 5.45 (s, 1 H).
Step 2; 3-(Amino(phenyl)methyl)phenol hydrochloride Methanol (125 mL), was cooled to 0°C and acetyl chloride (17.8 mL) added dropwise to give a 2M solution of methanolic hydrogen chloride.
N-((3-hydroxyphenyl)(phenyl)methyl)formamide was stirred at 40°C for 1.5 hours with the 2M methanolic hydrogen chloride. The solvent was removed under reduced pressure and the residue re-dissolved in methanol and the solvent removed under reduced pressure. This process was repeated three times to give the title compound (29.09 g, 97.9%) ¹H NMR (400 MHz, DMSO-d6): δ 9.76 (s, 1 H); 9.07 (s, 3 H); 7.59-7.53 (m, 2 H); 7.51-7.37 (m, 3 H); 7.26 (t, J = 7.89 Hz, 1 H); 6.99 (d, J = 7.75 Hz, 1 H); 6.90 (t, J = 1.97 Hz, 1 H); 6.81 (dd, J = 8.10, 2.32 Hz, 1 H); 5.58 (d, J = .82 Hz, 1 H).
Step2a; Synthesis of enantiomerically pure 3- 149 (Amino(phenyl)methyl)phenol Mandelate (fast eluting enantiomer) 3-(Amino(phenyl)methyl)phenol (878 g, 4.4 mol) was dissolved in 17.5 l of iPrOH and heated to reflux. To the mixture a solution of R-mandelic acid (737 g, 4.8 mol) in 1760 ml of iPrOH was dropped. The mixture was refluxed for 1 h and then allowed to cool to 10°C (overnight). The precipitate was filtered, washed with cold iPrOH and dried in vacuum oven at 35°C. The collected salt was refluxed in 95% iPrOH for 1h, then slowly cooled to 70°C (beginning of crystallization) and stirred at constant temperature for 5h. The mixture was allowed to cool down to 10°C overnight. The solid was filtered, washed with cold iPrOH and dried in vacuum oven at 35°C.
Chiral analyses were made for free amine (the salt treated with sodium hydrogen carbonate, extracted with AcOEt and the organic layer concentrated).
Chiralpak IC, 4.6mmx250mm - (A) Ethanol + 0.1% TEA (B) Hexane + 0.1% TEA flow: 1ml/min (10%A; 90%B) ee >99% retention time 10.58 min 1H NMR (600 MHz, d6-DMSO) 4.65 (s, 1H), 5.34 (s, 1H), 6.70 (m, 1H, Ar), 6.82 (m, 1H, Ar), 6.86 (m, 1H, Ar), 7.12 (m, 1H, Ar), 7.18 (m, 1H, Ar), 7.23-7.29 (m, 3H, Ar), 7.33-7.38 (m, 4H, Ar), 7.42 (m, 2H, Ar).
A sample of amine was converted into the corresponding hydrochloride. [ ] = α D -0.019º (c=4.4, MeOH) A sample of amine was converted into the corresponding BOC derivatives as described in following Step 3 and analized by chiral HPLC that confirmed identical retention time of fast eluting enantiomer BOC protected.
Step2b; Synthesis of enantiomerically pure 3-(Amino(phenyl)methyl)phenol Mandelate (slow eluting enantiomer) The product was prepared as described in Step 2a using S-mandelic acid. 150 ee >99% retention time 16.37 min A sample of amine was converted into the corresponding hydrochloride. [ ] = α D +0.019º (c=4.4, MeOH) A sample of amine was converted into the corresponding BOC derivatives as described in following Step 3 and analized by chiral HPLC that confirmed identical retention time of slow eluting enantiomer BOC protected.
Step 3; tert-Butyl (3-hydroxyphenyl)(phenyl)methylcarbamate 3-(Amino(phenyl)methyl)phenol hydrochloride (29.09 g, 123.4 mmol) in dichloromethane (450 mL) was cooled to 0°C and diisopropylethylamine (65.9 mL, 370.2 mmol) and di-tert-butyl dicarbonate (59.2 g, 271.5 mmol) was added slowly. The reaction was stirred at 0°C for 2 hours then warmed to room temperature over 16 hours. The solvent was removed and compound purified through a silica plug, eluting with 0-20% ethyl acetate in iso-hexane to give a black oil. To this mixture in methanol (300 mL) was added potassium carbonate (51 g, 370.2 mmol) and stirred at room temperature for 16 hours. The suspension was filtered and the filtrate was evaporated at reduced pressure and the residue re-dissolved in ethyl acetate (370 mL). Silica (73 g) was added and the suspension was stirred for 30 minutes, filtered, and the filter cake washed with further ethyl acetate. The filtrate was evaporated to dryness. The dark solid residue was dissolved in ethyl acetate (200 m L) was charcoal added and the suspension was heated under refluxed for 1 hour. The suspension was filtered through celite and solvent removed. The dark solid was dissolved in dichloromethane and iso-hexane added then solvent evaporated (repeated 3 times) to give the title compound (34.81 g, 92%).
¹H NMR (400 MHz, CDCl3-d): δ 7.36-7.16 (m, 6 H); 6.80 (d, J = 7.79 151 Hz, 1 H); 6.74-6.69 (m, 2 H); 5.83 (s, 1 H); 5.15 (s, 1 H); 1.53-1.30 (s, 9 H).
Step 4; Resolution of the racemic mixture into first and second eluting isomers The racemic mixture was purified by SFC using a CHIRALPAK® AD 20 µM 250 x 110 mm column using n-heptane / 2-propanol / diethylamine (60 / 40/ 0.1) as eluant with a flow rate of 570 ml / min at 25°C. From 54.1 g of crude material the first eluting enantiomer (Rt = 4.5 min, 26.7 g, >99.9% e.e.) and second eluting isomer (Rt = 8.5-8.6 min, 23.9 g, 99.2 e.e.) were separated.
Step 5; tert-Butyl ((3-((5-(1,3-dioxolan yl)pentyl)oxy)phenyl)(phenyl)methyl)carbamate Potassium carbonate (0.566 g, 4.10 mmol) was added to a solution of tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate (derived from the first eluting isomer, 0.614 g, 2.05 mmol) in acetonitrile (6 mL). The reaction mixture was stirred at ambient temperature for 10 minutes and 2-(5-bromopentyl)-1,3-dioxolane (0.549 g, 2.46 mmol) added. The reaction mixture was heated at 60°C for 20 hours. The reaction mixture was allowed to cool and diluted with water and DCM. The mixture was poured through a hydrophobic frit and the organic phase was evaporated at reduced pressure.
The crude material was purified by silica gel chromatography eluting with 100% iso-hexane to 10% ethyl acetate in iso-hexane to afford the title compound as a colourless oil (0.503 g, 56%).
¹H NMR (400 MHz, CDCl3): δ 7.34-7.13 (m, 6 H); 6.81-6.76 (m, 3 H); .85 (br s, 1 H); 5.10 (br s, 1 H); 4.86 (t, J = 4.8 Hz, 1 H); 3.97-3.83 (m, 6 H); 152 1.78-1.66 (m, 4 H); 1.50-1.44 (m, 4 H), 1.30 (s, 9 H).
Step 6; (3-((6,6-Dimethoxyhexyl)oxy)phenyl)(phenyl)methanamine To a solution of tert-butyl ((3-((5-(1,3-dioxolan yl)pentyl)oxy)phenyl)(phenyl)methyl)carbamate (0.483 g, 1.10 mmol) in methanol (4 mL) was added hydrogen chloride in dioxane (4 M, 4 mL, 16 mmol). The reaction was stirred at ambient temperature for 7 hours. The solvent was evaporated at reduced pressure and the residue loaded onto an SCX-2 cartridge. The cartridge was eluted with methanol (eight column volumes) followed by ammonia/methanol. Fractions containing the product were combined and evaporated at reduced pressure to afford the title compound as a colourless oil (0.322 g, 85%).
¹H NMR (400 MHz, CDCl3): δ 7.38-7.18 (m, 6 H); 6.94-6.92 (m, 2 H); 6.73-6.73 (m, 1 H); 5.17 (s, 1 H); 4.38 (t, J = 5.6 Hz, 1 H); 3.93 (t, J = 6.4 Hz, 2 H); 3.32 (s, 6 H); 1.80-1.73 (m, 4 H); 1.65-1.60 (m, 2 H); 1.49-1.40 (m, 4 H).
Step 7; (R)-quinuclidinyl ((3-((6-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(phenyl)- methyl)carbamate (compound 41B) The title compound was prepared using Step 5, 6 and 7 of Example 1.
Chiral Example 2 (R)-Quinuclidinyl ((3-((6-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(phenyl)- methyl)carbamate (compound 42B) 153 The title compound was prepared as in Chiral Example 1 with the second eluting isomer from Step 4 used in Step 5.
Chiral Example 3 (3R)((((3-((6-(((R)Hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(phenyl)methyl)- carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 43B) N H N H O OH HO O N H O O N + O The title compound was prepared as in Example 24 with Chiral Example 1 replacing (R)-quinuclidinyl (3-(6-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyloxy)phenyl)(phenyl)methylcarbamate.
Chiral Example 4 (3R)((((3-((6-(((R)Hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(phenyl)methyl)- carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium (compound 44B) The title compound was prepared as in Example 24 with Chiral Example 2 replacing (R)-quinuclidinyl (3-(6-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethylamino)hexyloxy)phenyl)- (phenyl)methylcarbamate.
Chiral Example 5 4-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 154 yl)ethyl)amino)butyl 4-((3-(phenyl((((R)-quinuclidinyloxy)carbonyl)- amino)methyl)phenoxy)methyl)benzoate (compound 45B) Step 1; 3-(1,3-Dioxolanyl)propyl 4-(hydroxymethyl)benzoate To a stirred solution of 4-hydroxymethylbenzoic acid (3.33 g, 21.9 mmol) in DMF (100 mL) was added potassium carbonate (5.67 g, 41.04 mmol) followed by 2-(3-bromopropyl)-1,3-dioxolane (3.0 g, 19.9 mmol). The resulting mixture was heated at 80°C for 16 hours. The reaction mixture was diluted with ethyl acetate and washed sequentially with water and twice with brine. The organic phase was dried with anhydrous magnesium sulphate, filtered and the filtrate evaporated at reduced pressure.
The crude material was purified by silica gel chromatography eluting with 100% iso-hexane to 100% ethyl acetate in iso-hexane to afford the title compound as a colourless oil (2.55 g, 48%).
¹H NMR (400 MHz, CDCl3): δ 8.06-7.98 (m, 2 H); 7.44 (d, J = 8.0 Hz, 2 H); 4.96-4.88 (m, 1 H); 4.77 (d, J = 4.0 Hz, 2 H); 4.36 (t, J = 6.4 Hz, 2 H); 4.02-3.94 (m, 2 H); 3.92-3.81 (m, 2 H); 1.96-1.80 (m, 4 H).
Step 2; 3-(1,3-Dioxolanyl)propyl 4-((3-(((tert20 butoxycarbonyl)amino)(phenyl)methyl)phenoxy)methyl)benzoate The title compound was prepared as described in Example 22 Step 2 155 with 3-(1,3-dioxolanyl)propyl 4-(hydroxymethyl)benzoate and tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate (first eluting isomer from Chiral Example 1 Step 4) replacing (4-((1,3-dioxolanyl)methyl)phenyl)methanol and 3-hydroxybenzophenone respectively.
¹H NMR (400 MHz, CDCl3): δ 8.04-8.02 (m, 2 H); 7.47-7.45 (m, 2 H); 7.33-7.21 (m, 6 H); 6.88-6.84 (m, 3 H); 5.87 (br s, 1 H); 5.15 (br s, 1 H); 5.08 (s, 2 H); 4.95-4.93 (m, 1 H); 4.38-4.35 (m, 2 H); 4.10-3.97 (m, 2 H); 3.88-3.85 (m, 2 H); 1.94-1.90 (m, 2 H); 1.86-1.83 (m, 2 H), 1.30 (s, 9 H).
Step 3; 3-(1,3-Dioxolanyl)propyl 4-((3- (amino(phenyl)methyl)phenoxy)methyl)benzoate hydrochloride Hydrogen chloride in dioxane (4.0 M, 6 mL, 24 mmol) was added to 3-(1,3-dioxolanyl)propyl 4-((3-(((tert-butoxycarbonyl)amino)(phenyl)- methyl)phenoxy)methyl)benzoate (0.756 g, 1.38 mmol) and the resultant solution was stirred at ambient temperature for 2 hours. The solvent was evaporated at reduced pressure to afford the title compound (0.750 g, 100%).
Step 4; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin5-yl)ethyl)amino)butyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate (compound 45B) The title compound was prepared using Step 5, 6 and 7 of Example 1.
Chiral Example 6 4-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 156 yl)ethyl)amino)butyl 4-((3-(phenyl((((R)-quinuclidinyloxy)carbonyl)- amino)methyl)phenoxy)methyl)benzoate (compound 46B) The title material was prepared as described in Chiral Example 5 with tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate (second eluting isomer from Chiral Example 1 Step 4) replacing tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate (first eluting isomer from Chiral Example 1 Step 4) in Step 2.
An alternative method to prepare the key intermediate A in Chiral Example 5 or Chiral Example 6 is detailed below. The example below details the use of the second eluting isomer derived from Chiral Example 1 Step 4.
Step 1; Methyl 4-((3-(((tert-butoxycarbonyl)amino)- (phenyl)methyl)phenoxy)methyl)benzoate The title compound was prepared as described in Example 106 Step 4 with the second eluting isomer from Chiral Example 1 Step 4 replacing tert- 157 butyl (3-hydroxyphenyl)(phenyl)methylcarbamate.
¹H NMR (400 MHz, CDCl3): δ 8.04 (d, J = 8.2 Hz, 2 H); 7.46 (d, J = 8.2 Hz, 2 H); 7.34-7.20 (m, 6 H); 6.90-6.81 (m, 3 H); 5.87 (s, 1 H); 5.13 (s, 1 H); 5.07 (s, 2 H); 3.92 (s, 3 H); 1.44 (s, 9 H).
Step 2; 4-((3-(((tert-Butoxycarbonyl)amino)(phenyl)methyl)- phenoxy)methyl)benzoic acid The title compound was prepared as described in Example 81 Step 7 with methyl 4-((3-(((tert-butoxycarbonyl)amino)(phenyl)methyl)phenoxy)- methyl)benzoate replacing methyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate.
¹H NMR (DMSO-d6): δ 7.94 (3 H, m), 7.54 (2 H, d, J = 7.97 Hz), 7.43 (1 H, d, J = 7.98 Hz), 7.37-7.15 (5 H, m), 7.02 (1 H, s), 6.96-6.84 (2 H, m), .79 (1 H, d, J = 9.68 Hz), 5.16 (2 H, s), 1.39 (9 H, s) Step 3; 3-(1,3-Dioxolanyl)propyl 4-((3-(((tertbutoxycarbonyl)amino)(phenyl)methyl)phenoxy)methyl)benzoate The title compound was prepared from 4-((3-(((tertbutoxycarbonyl)amino)(phenyl)methyl)phenoxy)methyl)benzoic acid and 2-(3-chloropropyl)-1,3-dioxolane according to the method of Chiral Example Step 1. 158 ¹H NMR (400 MHz, CDCl3): δ 8.04-8.02 (m, 2 H); 7.47-7.45 (m, 2 H); 7.33-7.21 (m, 6 H); 6.88-6.84 (m, 3 H); 5.87 (br s, 1 H); 5.15 (br s, 1 H); 5.08 (s, 2 H); 4.95-4.93 (m, 1 H); 4.38-4.35 (m, 2 H); 4.10-3.97 (m, 2 H); 3.88-3.85 (m, 2 H); 1.94-1.90 (m, 2 H); 1.86-1.83 (m, 2 H), 1.30 (s, 9 H).
The following compounds were made using this alternative synthesis starting from the second eluting isomer of tert-butyl (3- hydroxyphenyl)(phenyl)methylcarbamate using the appropriate alkylating agent in Step 1.
Compound LINKER Appropriate alkylating agent 47C 48C 49C 50C 51C 52C Chiral Example 7 -(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 159 yl)ethyl)amino)pentyl 2-(3-(phenyl((((R)-quinuclidinyloxy)- carbonyl)amino)methyl)phenoxy)acetate (Compound 53C) HN OH HN O HO O O O H N O O N The title compound was prepared as described in Compound 9C but starting from the second eluting isomer from Chiral Example 1 Step 4.
Chiral Example 8 5-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl 2-(3-(phenyl((((R)-quinuclidinyloxy)- carbonyl)amino)methyl)phenoxy)acetate (Compound 54C) The title compound was prepared as described in Compound 9C but starting from the first eluting isomer from Chiral Example 1 Step 4.
Chiral Example 9 6-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)hexyl 2-(3-(phenyl((((R)-quinuclidinyloxy)carbonyl)- amino)methyl)phenoxy)acetate (Compound 55C) The title compound was prepared as described in Example 59 but starting from the second eluting isomer from Chiral Example 1 Step 4.
Chiral Example 10 6-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 160 yl)ethyl)amino)hexyl 2-(3-(phenyl((((R)-quinuclidinyloxy)carbonyl)- amino)methyl)phenoxy)acetate (Compound 56C) The title compound was prepared as described in Example 59 but starting from the first eluting isomer from Chiral Example 1 Step 4.
Chiral Example 11 (R)-Quinuclidinyl ((3-((4-((3-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)propyl)carbamoyl)benzyl)oxy)- phenyl)(phenyl)methyl)carbamate (Compound 57C) Step 1; 4-((3-(Phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoic acid The title compound was prepared as described in Example 79 Steps 4-7 with the second eluting isomer from Chiral Example 1 Step 4 replacing the racemic tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate in Step 4.
Step 2; (R)-Quinuclidinyl ((3-((4-((3,3- diethoxypropyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate 161 To a stirred solution of 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoic acid (0.300 g, 0.57 mmol) in DMF (2.5 mL) was added HATU (0.262 g, 0.69 mmol) and diisopropylethylamine (0.250 mL, 1.43 mmol) and the reaction mixture was stirred at room temperature for 30 minutes. 1-Amino-3,3-diethoxypropane (0.139 mL, 0.86 mmol) was added and the reaction mixture was stirred at room temperature for 18 hours. The reaction mixture was diluted with ethyl acetate and washed sequentially with saturated sodium hydrogen carbonate and brine (x2). The organic phase was died with anhydrous sodium sulphate, filtered and the solvent evaporated at reduced pressure. The crude material was purified by silica gel chromatography eluting with 100% iso-hexane to 100% ethyl acetate in iso-hexane to afford the title compound (0.347 g, 99%), used directly in the next step.
Step 3; (R)-quinuclidinyl ((3-((4-((3-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)propyl)carbamoyl)- benzyl)oxy)phenyl)(phenyl)methyl)carbamate The title compound was prepared as described in Example 1 Step 6 and Step 7.
The following compounds were prepared in the same fashion as Chiral Example 11 using the appropriate amine in Step 2. 162 Compound No Linker Appropriate amine 58C 59C 60C 61C 62C 63C 64C 65C 66C The amines for Compounds 59C, 60C, 61C, 65C and 66C were prepared as detailed below (exemplified for the amine for Compound 60C); N-Benzylmethyalmine (1 equivalent), 2-(2-bromoethyl)-1,3-dioxalane (1.5 equivalents) and potassium carbonate (1.5 equivalents) in acetonitrile 163 (0.4 M) were heated at 80°C for 24 hours. The reaction mixture was diluted with ethyl acetate and washed sequentially with water and saturated aqueous brine. The organic phase was dried with anhydrous magnesium sulfate, filtered and the solvent evaporated at reduced pressure. The residue was purified by chromatography on an SCX-2 cartridge. The material was subjected to the procedure described in the synthesis of (R)(2-Amino (tert-butyldimethylsilyloxy)ethyl)hydroxyquinolin-2(1H)-one.
The amine for Compound 62C was prepared by alkylating trans (((tert-butoxycarbonyl)amino)methyl)cyclohexanecarboxylic acid with 2-(3-chloropropyl)-1,3-dioxolane according to the protocol in Example 54 Step 1 followed by removal of the protecting group according to the protocol in Example 81 Step 5.
The amine for Compound 63C was prepared by coupling (S)((tertbutoxycarbonyl)amino)methoxyoxobutanoic acid and 2,2-dimethoxy-N15 methylethanamine according to the protocol in Chiral Example 11 Step 2 followed by removal of the protecting group according to the protocol in Example 81 Step 5.
The following compounds were prepared in a similar fashion to Chiral Example 11 but using the appropriate alcohol (heated at 60°C) in Step 2.
Compound No Linker Appropriate alcohol 67C (continued) 164 68C 69C 70C 71C O O OH O O 72C 73C 74C The alcohol required to prepare Compound 67C was prepared as described in Faming Zhuanli Shenqing Gongkai Shuomingshu, 101153000, 02 Apr 2008.
The alcohol required to prepare Compound 68C and 69C was prepared from the requisite amine and hydroxyacetic acid.
The alcohol required to prepare Compound 70C and 71C was prepared from the requisite alcohol and hydroxyacetic acid.
The alcohol required to prepare Compound 72C and 73C was prepared from ethylene glycol and the requisite bromide.
Chiral Example 12 3-(3-(Phenyl((((R)-quinuclidinyloxy)carbonyl)amino)methyl)- phenoxy)propyl 4-(2-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)ethyl)benzoate (Compound 75C) Step 1; 3-(3-(((tert-Butoxycarbonyl)amino)(phenyl)methyl)- 165 phenoxy)propyl benzoate The title compounds was prepared as described in Example 22 Step 3 with 3-hydroxypropyl benzoate (prepared as outlined in Organic & Biomolecular Chemistry, 8(24), 5505-5510; 2010) and tert-butyl ((3-hydroxyphenyl)(phenyl)methyl)carbamate (derived from the second eluting isomer Chiral Example 1 Step 4) replacing (4-((1,3-dioxolan yl)methyl)phenyl)methanol and 3-hydroxybenzophenone respectively.
¹H NMR (400 MHz, CDCl3): δ 8.03 (d, J = 7.7 Hz, 2 H); 7.60-7.52 (m, 1 H); 7.48-7.40 (m, 2 H); 7.35-7.19 (m, 6 H);6.85-6.76 (m, 3 H); 5.86 (s, 1 H); .13 (s, 1 H); 4.54-4.47 (m, 2 H); 4.16-4.05 (m, 2 H); 2.29-2.19 (m, 2 H); 1.43 (s, 9 H).
Step 2; 3-(3-(Amino(phenyl)methyl)phenoxy)propyl benzoate hydrochloride Hydrogen chloride in dioxane (4 M, 3.30 mL, 13.2 mmol) was added to 3-(3-(((tert-butoxycarbonyl)amino)(phenyl)methyl)phenoxy)propyl benzoate (0.359 g, 0.78 mmol) and the resultant mixture was stirred at room temperature for 2 hours. The solvent was evaporated at reduced pressure to afford the title compound (0.271 g, 88%).
¹H NMR (400 MHz, DMSO-d6): δ 8.95 (s, 3 H); 7.98 (d, J = 7.7 Hz, 2 H); 7.71-7.63 (m, 1 H); 7.52 (dd, J = 15.3, 7.6 Hz, 4 H); 7.46-7.29 (m, 4 H); 7.17 (s, 1 H); 7.05 (d, J = 7.7 Hz, 1 H); 6.96 (d, J = 8.3 Hz, 1 H); 5.60 (s, 1 H); 4.47-4.40 (m, 2 H); 4.18-4.11 (m, 2 H); 2.24-2.16 (m, 2 H).
Step 3; 3-(3-(Phenyl((((R)-quinuclidin 166 yloxy)carbonyl)amino)methyl)phenoxy)propyl benzoate The title compound was prepared as described in Example 1 Step 5 with 3-(3-(amino(phenyl)methyl)phenoxy)propyl benzoate hydrochloride replacing (3-(8-(1,3-dioxolanyl)octyloxy)phenyl)(phenyl)methanamine.
¹H NMR (400 MHz, CDCl3): δ 8.05-8.00 (m, 2 H); 7.60-7.53 (m, 1 H); 7.48-7.40 (m, 2 H); 7.37-7.29 (m, 2 H); 7.28-7.18 (m, 4 H); 6.88-6.78 (m, 3 H); 5.91 (s, 1 H); 5.31 (s, 1 H); 4.72 (s, 1 H); 4.54-4.47 (m, 2 H); 4.16-4.06 (m, 2 H); 3.20 (s, 1 H); 2.93-2.63 (s, 4 H); 2.28-2.19 (m, 2 H); 2.03-1.48 (br, 6 H).
Step 4; (R)-Quinuclidinyl ((3-(3-hydroxypropoxy)phenyl)- (phenyl)methyl)carbamate H N HO O O O N To a stirred solution of 3-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)propyl benzoate (0.370 g, 0.72 mmol) in methanol (3.6 mL) was added a solution of lithium hydroxide monohydrate (0.060 g, 1.44 mmol) in water (1.2 mL). The reaction mixture was stirred at room temperature for 1 hour. Further lithium hydroxide monohydrate (0.060 g, 1.44 mmol) was added and the reaction stirred at room temperature for a further 16 hours. The reaction mixture was heated at 40°C for 3.5 hours and allowed to cool. The solvent was evaporate at reduced pressure and the residue partitioned between ethyl acetate and water. The aqueous phase was further extracted with ethyl acetate (x2). The combined organic extracts were washed with 10% aqueous potassium carbonate (x2), saturated brine and dried 167 with anhydrous sodium sulfate. The mixture was filtered and the solvent evaporated at reduced pressure to afford the title compound (0.275 g, 93%).
¹H NMR (400 MHz, CDCl3): δ 7.38-7.20 (m, 6 H); 6.83 (t, J = 8.5 Hz, 3 H); 5.91 (s, 1 H); 5.30 (s, 1 H); 4.72 (s, 1 H); 4.16-4.06 (m, 2 H); 3.83 (t, J = 5.8 Hz, 2 H); 3.19 (s, 1 H); 2.94-2.62 (m, 4 H); 2.04-1.96 (m, 2 H); 1.90-1.32 m, 7 H).
Step 5; 3-(3-(Phenyl((((R)-quinuclidinyloxy)carbonyl)amino)- methyl)phenoxy)propyl 4-((1,3-dioxolanyl)methyl)benzoate The title compound was prepared as described in Chiral Example 11 Step 2 with (R)-quinuclidinyl ((3-(3-hydroxypropoxy)phenyl)- (phenyl)methyl)carbamate and 4-(1,3-dioxolanylmethyl)-benzoic acid replacing 4-((3-(phenyl((((R)-quinuclidinyloxy)carbonyl)amino)- methyl)phenoxy)methyl)benzoic acid and 1-amino-3,3-diethoxypropane respectively.
Step 6; 3-(3-(Phenyl((((R)-quinuclidinyloxy)carbonyl)amino)- methyl)phenoxy)propyl 4-(2-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)ethyl)benzoate (Compound 75C) The title compound was prepared as described in Example 1 Step 6 and 7.
Chiral Example 13 4-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-(2-(3-(phenyl((((R)-quinuclidinyloxy)carbonyl)- 168 amino)methyl)phenoxy)ethyl)benzoate (Compound 76C) The title compound was prepared as in Chiral Example 5 with 4-(2-hydroxyethyl)benzoic acid replacing 4-hydroxymethylbenzoic acid and using tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate (second eluting isomer from Chiral Example 1 Step 4) in Step 1.
Chiral Example 14 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-(5-((3-(phenyl((((R)-quinuclidinyloxy)carbonyl)- amino)methyl)phenoxy)methyl)-1,2,4-oxadiazolyl)benzoate (Compound 77C) Step 1; 3-(1,3-Dioxolanyl)propyl 4-cyanobenzoate The title compound was prepared as described in Chiral Example 4 Step 1 with 4-cyanobenzoic acid replacing 4-hydroxymethylbenzoic acid.
¹H NMR (400 MHz, CDCl3): δ 8.16-8.12 (m, 2 H); 7.77-7.73 (m, 2 H); 4.97-4.89 (m, 1 H); 4.44-4.36 (m, 2 H); 4.04-3.83 (m, 4 H); 1.97-1.88 (m, 2 H); 1.86-1.79 (m, 2 H).
Step 2; 3-(1,3-Dioxolanyl)propyl 4-(N'- hydroxycarbamimidoyl)benzoate 169 To a solution of 3-(1,3-dioxolanyl)propyl 4-cyanobenzoate (1.00 g, 4.38 mmol) in ethanol (5 mL) was added hydroxylamine (50% aqueous solution, 5 mL) and the mixture heated at 80°C for 4 hours. The reaction was diluted with saturated brine and extracted with ethyl acetate (x3). The combined organic fractions were dried with magnesium sulfate and the solvent evaporated at reduced pressure. Material used directly in the next step without further purification.
Step 3; Methyl 2-(3-(((tert-butoxycarbonyl)amino)- (phenyl)methyl)phenoxy)acetate The title compound was prepared as described in Example 79 Step 4 with the second eluting isomer from Chiral Example 1 Step 4 replacing tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate.
Step 4; 2-(3-(((tert-Butoxycarbonyl)amino)- (phenyl)methyl)phenoxy)acetic acid The title compound was prepared as described in Example 79 Step 7 with methyl 2-(3-(((tert-butoxycarbonyl)amino)(phenyl)methyl)phenoxy)- acetate acid replacing methyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate. 170 Step 5; 3-(1,3-Dioxolanyl)propyl 4-(5-((3-(((tert-butoxycarbonyl)- amino)(phenyl)methyl)phenoxy)methyl)-1,2,4-oxadiazolyl)benzoate To a solution of 2-(3-(((tert-butoxycarbonyl)amino)(phenyl)- methyl)phenoxy)acetic acid (0.087 g. 0.34 mmol) and 3-(1,3-dioxolan yl)propyl 4-(N'-hydroxycarbamimidoyl)benzoate (0.10 g, 0.28 mmol) in acetonitrile (1 mL) was added 1-ethyl(3-dimethyllaminopropyl)- carbodiimide hydrochloride (0.087 g, 0.42 mmol). The reaction mixture was stirred at ambient temperature for 16 hours. The reaction mixture was diluted with pyridine and heated at 150°C for 30 minutes in a microwave. The reaction was diluted with saturated brine and extracted with ethyl acetate (x3).
The combined organic fractions were dried with magnesium sulfate and the solvent evaporated at reduced pressure. Material used directly in the next step without further purification (0.142 g, 87%).
¹H NMR (400 MHz, CDCl3): δ 8.16 (s, 4H); 7.40-7.33 (m, 6 H); 7.00-6.88 (m, 3 H); 5.35-5.26 (m, 2 H); 4.97-4.92 (m, 1 H); 4.45-4.35 (m, 2 H); 4.04-3.93 (m, 2 H); 3.93-3.83 (m, 2 H); 2.01-1.81 (m, 4 H); 1.43 (s, 9 H).
Step 6; 3-(1,3-dioxolanyl)propyl 4-(5-((3- (amino(phenyl)methyl)phenoxy)methyl)-1,2,4-oxadiazolyl)benzoate hydrochloride Hydrogen chloride in dioxane (4.0 M, 5 mL, 24 mmol) was added to 3-(1,3-dioxolanyl)propyl 4-(5-((3-(((tert-butoxycarbonyl)amino)(phenyl)- methyl)phenoxy)methyl)-1,2,4-oxadiazolyl)benzoate (0.237 g, 0.41 mmol) and the resultant solution was stirred at ambient temperature for 2 hours. The 171 solvent was evaporated at reduced pressure to afford the title compound (0.212 g, 100%).
¹H NMR (400 MHz, DMSO-d6): δ 9.05 (s, 3 H); 8.18-8.07 (m, 4 H); 7.50 (d, J = 7.6 Hz, 2 H); 7.42-7.30 (m, 5 H); 7.15 (d, J = 7.8 Hz, 1 H); 7.10 (dd, J = 8.3, 2.6 Hz, 1 H); 5.71-5.53 (m, 3 H); 4.86-4.81 (m, 1 H); 4.35-4.27 (m, 2 H); 3.91-3.81 (m, 2 H); 3.79-3.73 (m, 2 H); 1.86-1.68 (m, 4 H).
Step 7; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin5-yl)ethyl)amino)butyl 4-(5-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)-1,2,4-oxadiazol yl)benzoate (Compound 77C) The title compound was prepared using Step 5, 6 and 7 of Example 1.
Chiral Example 15 4-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-((4-((3-(phenyl((((R)-quinuclidinyloxy)- carbonyl)amino)methyl)phenoxy)methyl)piperidinyl)methyl)benzoate (Compound 78C) Step 1; Benzyl 4-((3-(((tert-butoxycarbonyl)amino)- (phenyl)methyl)phenoxy)methyl)piperidinecarboxylate 172 To a stirred solution of tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate.(the second eluting isomer from Chiral Example 1 Step 4, 1.00 g, 3.34 mmol) in DMF (15 mL) was added potassium carbonate (0.554 g, 4.01 mmol). The reaction mixture was stirred for 10 minutes and benzyl 4-((tosyloxy)methyl)piperidinecarboxylate (prepared according to Bioorganic & Medicinal Chemistry Letters, 20(1), 380-382; 2010, 1.48 g, 3.67 mmol) added. The reaction mixture was heated at 60°C for 2 days followed by 80°C for 5 days. The reaction mixture was diluted with ethyl acetate and washed with water and saturated brine (x2). The organic phase was dried with anhydrous magnesium sulfate and the solvent evaporated at reduced pressure. The crude material was purified by silica gel chromatography eluting with 100% iso-hexane to 50% ethyl acetate in iso-hexane to afford the title compound (1.12 g, 63%).
¹H NMR (400 MHz, CDCl3): δ 7.40-7.18 (m, 11 H); 6.82 (d, J = 7.7 Hz, 1 H); 6.79-6.73 (m, 2 H); 5.86 (s, 1 H); 5.13 (s, 3 H); 4.23 (s, 2 H); 3.76 (d, J = 6.3 Hz, 2 H); 2.81 (m, 2 H); 1.99-1.89 (m, 1 H); 1.82 (d, J = 13.1 Hz, 2 H); 1.44 (s, 9 H); 1.33-1.22 (m, 2 H).
Step 2; tert-Butyl (phenyl(3-(piperidin ylmethoxy)phenyl)methyl)carbamate To a stirred solution of benzyl 4-((3-(((tertbutoxycarbonyl)amino)(phenyl)methyl)phenoxy)methyl)piperidine carboxylate (1.12 g, 2.11 mmol) in ethanol (10 mL) was added 10% palladium on charcoal (0.22 g) and 1-methyl1,4-cyclohexadiene (1.18 mL, 10.55 mmol).
The reaction mixture was heated to 80°C for 7 hours. The reaction mixture was filtered through a pad of celite and the filter-pad washed with further 173 ethanol. The filtrate was evaporated at reduced pressure to afford the title compound (0.716 g, 85%).
¹H NMR (400 MHz, CDCl3): δ 7.38-7.17 (m, 6 H); 6.82-6.73 (m, 3 H); .86 (s, 1 H); 5.15 (s, 1 H); 3.78-3.68 (m, 2 H); 3.13 (d, J = 12.3 Hz, 2 H); 2.65 (td, J = 12.1, 2.5 Hz, 2 H); 1.96-1.78 (m, 5 H); 1.33-1.18 (m, 9 H) (no exchangeable observed) Step 3; 3-(1,3-Dioxolanyl)propyl 4-((4-((3-(((tertbutoxycarbonyl)amino)(phenyl)methyl)phenoxy)methyl)piperidin yl)methyl)benzoate To a stirred solution of tert-butyl (phenyl(3-(piperidin ylmethoxy)phenyl)methyl)carbamate (0.335 g, 0.84 mmol) and 3-(1,3-dioxolanyl)propyl 4-formylbenzoate (0.706 g, 2.67 mmol) in DCM (5 mL) was added sodium triacetoxyborohydride (0.213 g, 1.01 mmol). The reaction mixture was stirred at room temperature for 18 hours. The reaction mixture was diluted with DCM and washed with water, saturated aqueous sodium hydrogen carbonate and brine. The organic phase was dried with anhydrous magnesium sulfate and the solvent evaporated at reduced pressure.
The residue was triturated with iso-hexane/diethyl ether (3:1) to afford the title compound (0.286 g, 0.44 mmol).
¹H NMR (400 MHz, CDCl3): δ 7.98 (d, J = 8.0 Hz, 2 H); 7.39 (d, J = 8.0 Hz, 2 H); 7.35-7.16 (m, 6 H); 6.83-6.73 (m, 3 H); 5.86 (s, 1 H); 5.13 (s, 1 H); 4.96-4.91 (m, 1 H); 4.40-4.32 (m, 2 H); 4.00-3.95 (m, 2 H); 3.90-3.84 (m, 2 H); 3.76 (d, J = 5.8 Hz, 2 H); 3.55 (s, 2 H); 2.89 (d, J = 11.1 Hz, 2 H); 2.05- 1.97 (m, 2 H); 1.97-1.77 (m, 7 H); 1.63-1.19 (m, 11 H).
Step 4; 4-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin- 174 -yl)ethyl)amino)butyl 4-((4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)piperidin yl)methyl)benzoate (Compound 78C) The title compound was prepared as described in Chiral Example 5 Step 3 and 4.
The following compounds were prepared as described above using the first eluting isomer of tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate (Chiral Example 1 Step 4).
Chiral Example 16 2-(4-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butoxy)ethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate (Compound 79C) The title compound was prepared as described for Compound 73C using the first eluting isomer of tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate. 175 Chiral Example 17 4-(2-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethyl)benzyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)-amino)methyl)phenoxy)methyl)benzoate (Compound 80C) The title compound was prepared as described for Compound 8C using the first eluting isomer of tert-butyl (3-hydroxyphenyl)- (phenyl)methylcarbamate.
Chiral Example 18 2-(2-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethoxy)ethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate (Compound 81C) The title compound was prepared as described for Compound 72C using the first eluting isomer of tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate.
Chiral Example 19 4-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-chloro((3-(phenyl((((R)-quinuclidin 176 yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate (Compound 82C) The title compound was prepared as described for Compound 47C using the first eluting isomer of tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate.
Chiral Example 20 4-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-fluoro((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate (Compound 83C) 10 The title compound was prepared as described for Compound 48C using the first eluting isomer of tert-butyl (3-hydroxyphenyl)(phenyl)methylcarbamate.
Cpd. LCMS / HPLC method NMR data at 400 MHz Salt 1 B (CD3OD): δ 8.54 (s, 2 H); 8.37 (d, J = 9.88 Hz, 1 H); 7.36-7.18 (m, 7 H); 7.02 (d, J = 8.16 Hz, 1 H); 6.83-6.77 (m, 2 H); 6.68 (d, J = 9.88 Hz, 1 H); 5.86 (s, 1 H); 5.37 (dd, J = 7.81, 5.61 Hz, 1 H); 3.93 (t, J = 6.36 Hz, 2 H); 3.43 (d, J = 11.82 Hz, 1 H); 3.23- 3.04 (m, 3 H); 3.06-2.93 (m, 7 H); 2.19 (s, 1 H); 2.09 (s, 1 H); 1.88 (s, 1 H); 1.78-1.66 (m, 8 H); 1.46 (s, 3 H); 1.38 (s, 9 H) diformate 2 B (CD3OD): δ 8.56 (s, 2 H); 8.45-8.36 (m, 1 H); 7.38-7.20 (m, 7 H); 7.05 (d, J = 8.16 Hz, 1 H); 6.89-6.78 (m, 3 H); 6.70 (d, J = 9.84 Hz, 1 H); 5.88 (s, 1 H); 5.45-5.36 (m, 1 H); 4.90 (m, 1H, obscured by solvent); 3.95 (t, J = 6.34 Hz, 2 H); 3.59 (m, 1 H), 3.3-2.99 (m, 9 H), 2.30 (s, 1 H); 2.16 (s, 1 H); 2.03-1.69 (m, 7 H); 1.58-1.39 (m, 8 H) diformate (continued) 177 3 B (CD 3OD): δ 8.56 (s, 2 H); 8.40 (d, 1 H); 7.37-7.20 (m, 7 H); 7.04 (d, J = 8.16 Hz, 1 H); 6.89-6.78 (m, 3 H); 6.72 (d, 1 H); 5.88 (s, 1 H); 5.39 (t, J = 6.73 Hz, 1 H); 4.90 (m, 1H, obscured by solvent); 3.96 (t, J = 6.30 Hz, 2 H); 3.51 (m, 1 H); 3.22-2.98 (m, 9 H); 2.25 (s, 1 H); 2.13 (s, 1 H); 1.99- 1.64 (m, 7 H); 1.59-1.41 (m, 6 H) diformate 4 B (CD 3OD): δ 8.54 (s, 2H), 8.40 (d, J = 9.6 Hz, 1H), 7.36-7.23 (m, 7H), 7.05 (d, J = 8 Hz, 1H), 6.88-6.82 (m, 3H), 6.76 (d, J = 9.6 Hz, 1H), 5.88 (br s, 1H), 5.41-5.38 (m, 1H), 4.88 (m, 1H), 3.99-3.96 (m, 2H), 3.58 (m, 1H), 3.27-3.06 (m, 9H), 2.29 (br s, 1H), 2.17 (m, 1H), 1.98-1.73 (m, 6H), 1.60-1.45 (m, 5H) diformate B (DMSO-d 6): δ 8.32 (s, 2H), 8.27-8.25 (m, 1H), 8.21 (d, J = 10 Hz, 1H), 7.33-7.29 (m, 4H), 7.24-7.20 (m, 2H), 7.12 (d, J = 8.4 Hz, 1H), 6.98-6.90 (m, 3H), 6.80 (d, J = 8.0 Hz, 1H), 6.55 (d, J = 10 Hz, 1H), 5.82 (d, J = 8.8 Hz, 1H), 5.24-5.21 (m, 1H), 4.59 (br s, 1H), 3.94-3.91 (m, 2H), 3.13 (m, 1H), 2.91-2.33 (m, 8H), 1.93-1.39 (m, 12H) diformate 6 B (CD 3OD): δ 8.53 (s, 1 H), 8.38 (d, J = 9.87 Hz, 1 H), 7.45-7.21 (m, 12 H), 7.05 (d, J = 8.17 Hz, 1 H), 6.81 (s, 3 H), 6.70 (d, J = 9.84 Hz, 1 H), 5.86 (s, 1 H), 5.40 (t, J = 6.76 Hz, 1 H), 4.72 (s, 1 H), 3.95 (s, 2 H), 3.78 (s, 1 H), 3.26-3.20 (m, 2 H), 3.07 (t, J = 7.98 Hz, 2 H), 2.94 (s, 1 H), 2.60 (s, 2 H), 1.99 (s, 4 H), 1.84-1.71 (m, 6 H), 1.54- 1.30 (s, 10 H). formate 7 B (DMSO-d 6): δ 8.32 (s, 1 H); 8.20 (t, J = 9.75 Hz, 2 H); 7.35-7.26 (m, 4 H); 7.25- 7.16 (m, 2 H); 7.11 (d, J = 8.17 Hz, 1 H); 6.96 (d, J = 8.14 Hz, 1 H); 6.93-6.85 (m, 2 H); 6.77 (dd, J = 8.21, 2.42 Hz, 1 H); 6.53 (d, J = 9.86 Hz, 1 H); 5.81 (d, J = 9.40 Hz, 1 H); 5.21 (dd, J = 8.51, 4.13 Hz, 1 H); 4.51 (m, 1 H); 3.91 (t, J = 6.48 Hz, 2 H); 2.94-2.85 (m, 2 H); 2.79-2.72 (m, 2 H); 2.61 (s, 2 H); 2.24-1.97 (m, 5 H); 1.81 (s, 2 H); 1.72-1.62 (m, 2 H); 1.61-1.45 (m, 4 H); 1.44-1.14 (m, 10H) formate (continued) 178 8 A (DMSO-d6): δ 8.35 (s, 1 H); 8.19 (d, J = 9.86 Hz, 2 H); 7.37-7.15 (m, 10 H); 7.10 (d, J = 8.15 Hz, 1 H); 6.96 (d, J = 8.13 Hz, 1 H); 6.92-6.83 (m, 2 H); 6.77 (dd, J = 8.20, 2.50 Hz, 1 H); 6.52 (d, J = 9.84 Hz, 1 H); 5.79 (d, J = 9.39 Hz, 1 H); 5.18 (m, 1 H); 4.81 (m, 1 H); 3.91 (t, J = 6.50 Hz, 2 H); 3.54 (s, 2 H); 3.15 (d, J = 5.01 Hz, 2 H); 2.84 (m, 1 H); 2.73-2.65 (m, 1 H); 1.95 (s, 2 H); 1.79 (s, 2 H); 1.71-1.52 (m, 7 H); 1.49-1.21 (m, 13 H). formate 9 B (CD3OD): δ 8.55 (s, 2 H); 8.36 (d, J = 9.84 Hz, 1 H); 7.34-7.21 (m, 6 H); 7.14 (s, 3 H); 7.01 (d, J = 8.24 Hz, 1 H); 6.85 (d, J = 8.24 Hz, 2 H); 6.67 (d, J = 9.82 Hz, 1 H); 5.84 (s, 1 H); 5.39-5.32 (m, 1 H); 3.93 (t, J = 3.20 Hz, 2 H); 3.46-3.29 (m, 1 H); 3.19-3.14 (m, 2 H); 3.11-2.87 (m, 8 H); 2.17 (s, 1 H); 2.07 (s, 1 H); 1.86 (s, 1 H); 1.77-1.66 (m, 7 H); 1.47 (s, 3 H); 1.38 (s, 9 H). formate A (CD3OD): δ 8.39 (d, J = 9.83 Hz, 1 H); 7.34-7.17 (m, 3 H); 6.97-6.92 (m, 4 H); 6.90-6.80 (m, 2 H); 6.65 (d, J = 9.79 Hz, 1 H); 6.07 (s, 1 H); 5.25 (dd, J = 9.11, 3.86 Hz, 1 H); 4.74 (d, J = 7.36 Hz, 1 H); 3.97 (t, J = 6.39 Hz, 2 H); 3.28-3.14 (m, 1 H); 3.03-2.63 (m,9 H); 2.12-1.88 (m, 2 H); 1.84-1.70 (m, 3 H); 1.67-1.4 (m, 14 H) none 11 B (DMSO-d6): δ 8.34 (s, 1 H); 8.28 (d, J = 9.65 Hz, 1 H); 8.18 (d, J = 9.93 Hz, 1 H); 7.62 (t, J = 8.73 Hz, 4 H); 7.49-7.39 (m, 4 H); 7.35 (t, J = 7.35 Hz, 1 H); 7.23 (t, J = 7.90 Hz, 1 H); 7.10 (d, J = 8.16 Hz, 1 H); 6.95 (d, J = 8.34 Hz, 3 H); 6.79 (d, J = 8.37 Hz, 1 H); 6.52 (d, J = 9.86 Hz, 1 H); 5.86 (d, J = 9.33 Hz, 1 H); 5.17 (t, J = 6.14 Hz, 1 H); 4.59 (s, 1 H); 3.93 (t, J = 6.49 Hz, 2 H); 3.16-3.05 (m, 1 H); 2.86-2.81 (m, 2 H); 2.81-2.37 (m, 6 H); 1.92 (s, 1 H); 1.81 (s, 1 H); 1.74-1.11 (m, 18 H) formate 12 A (DMSO-d6): δ 8.35 (s, 2 H); 8.19 (d, J = 9.93 Hz, 1 H); 7.89-7.83 (m, 4 H); 7.54-7.45 (m, 3 H); 7.22 (t, J = 7.90 Hz, 1 H); 7.11 (d, J = 8.18 Hz, 1 H); 6.97 (d, J = 8.27 Hz, 3 H); 6.79 (d, J = 8.34 Hz, 1 H); 6.53 (d, J = 9.86 Hz, 1 H); 5.98 (s, 1 H); 5.22 (dd, J = 8.73, 4.00 Hz, 1 H); 4.61 (s, 1 H); 3.91 (t, J = 6.46 Hz, 2 H); 3.12 (m, 1 H); 2.94-2.81 (m, 2 H); 2.81- 2.54 (m, 4 H); 1.93 (s, 1 H); 1.81 (s, 1 H); 1.73-1.1 (m, 20 H) formate (continued) 179 13 A (DMSO-d6): δ 8.29 (d, J = 9.64 Hz, 1 H); 8.17 (d, J = 9.92 Hz, 1 H); 7.72-7.59 (m, 3 H); 7.52 (dd, J = 7.65, 1.84 Hz, 1 H); 7.48-7.31 (m, 5 H); 7.21 (t, J = 7.87 Hz, 1 H); 7.07 (d, J = 8.15 Hz, 1 H); 6.99-6.88 (m, 3 H); 6.77 (d, J = 8.21 Hz, 1 H); 6.50 (d, J = 9.86 Hz, 1 H); 5.89 (d, J = 9.31 Hz, 1 H); 5.03 (dd, J = 7.83, 4.59 Hz, 1 H); 4.57 (s, 1 H); 3.92 (t, J = 6.46 Hz, 2 H); 3.08 (s, 1 H); 2.78- 2.54 (m, 6 H); 1.90 (s, 1 H); 1.80 (s, 1 H); 1.72- 1.61 (m, 2 H); 1.57 (s, 1 H); 1.51-1.19 (m, 17 H) none 14 A (DMSO-d6): δ 8.51-8.48 (m, 1 H); 8.32 (s, 2 H); 8.19 (d, J = 9.9 Hz, 1 H); 8.10 (d, J = 9.1 Hz, 1 H); 7.80-7.73 (m, 1 H); 7.47 (d, J = 7.9 Hz, 1 H); 7.29-7.23 (m, 1 H); 7.19 (t, J = 7.9 Hz, 1 H); 7.10 (d, J = 8.2 Hz, 1 H); 6.99-6.87 (m, 3 H); 6.78 (d, J = 8.4 Hz, 1 H); 6.52 (d, J = 9.9 Hz, 1 H); 5.85 (d, J = 9.1 Hz, 1 H); 5.17 (t, J = 6.1 Hz, 1 H); 4.57 (m, 1 H); 3.91 (t, J = 6.8 Hz, 2 H); 3.16-3.04 (m, 1 H); 2.86-2.81 (m, 2 H); 2.79-2.38 (m, 4 H); 1.94-1.86 (m, 1 H); 1.86-1.73 (m, 1 H); 1.72-1.14 (m, 20 H). diformate B (DMSO-d6): δ 8.34-8.25 (m, 2 H); 8.18 (d, J = 9.9 Hz, 1 H); 7.23 (t, J = 7.9 Hz, 1 H); 7.16-7.06 (m, 4 H); 6.97-6.88 (m, 3 H); 6.81 (d, J = 8.3 Hz, 1 H); 6.52 (d, J = 9.9 Hz, 1 H); 5.86 (d, J = 9.2 Hz, 1 H); 5.15 (t, J = 6.3 Hz, 1 H); 4.62-4.55 (m, 1 H); 3.93 (t, J = 6.5 Hz, 2 H); 3.15-3.05 (m, 1 H); 2.83 (d, J = 6.3 Hz, 2 H); 2.80-2.44 (m, 4 H); 1.95-1.21 (m, 22 H). formate 16 B (DMSO-d6): δ 8.32-8.24 (m, 2 H); 8.18 (d, J = 9.9 Hz, 1 H); 7.41-7.33 (m, 2 H); 7.23 (t, J = 7.9 Hz, 1 H); 7.09 (d, J = 8.2 Hz, 1 H); 6.97-6.87 (m, 3 H); 6.81 (d, J = 8.3 Hz, 1 H); 6.52 (d, J = 9.9 Hz, 1 H); 5.85 (d, J = 9.0 Hz, 1 H); 5.14 (t, J = 6.3 Hz, 1 H); 4.61-4.55 (m, 1 H); 3.92 (t, J = 6.5 Hz, 2 H); 3.14-3.05 (m, 1 H); 2.81 (d, J = 6.3 Hz, 2 H); 2.79-2.45 (m, 4 H); 1.93-1.21 (m, 22 H). formate 17 B (DMSO-d6): δ 8.22-8.06 (m, 2 H); 7.22-7.13 (m, H); 7.04 (d, J = 8.14 Hz, 1 H); 6.87 (d, J = 8.11 Hz, 1 H); 6.80 (d, J = 7.85 Hz, 3 H); 6.48 (d, J = 9.85 Hz, 1 H); 5.97 (d, J = 8.81 Hz, 1 H); 4.99 (dd, J = 7.96, 4.44 Hz, 1 H); 4.54 (d, J = 7.42 Hz, 1 H); 3.93-3.86 (m, 2 H); 3.10-2.99 (m, 1 H); 2.74-2.60 (m, 6 H); 2.27 (d, J = 6.69 Hz, 3 H); 1.88 (s, 1 H); 1.77 (d, J = 13.00 Hz, 1 H); 1.73- 1.61 (m, 2 H); 1.56 (s, 2 H); 1.31 (d, J = 46.22 Hz, 16 H). none (continued) 180 18 A (DMSO-d6): δ 8.17 (d, J = 9.87 Hz, 2 H); 7.23-7.10 (m, 4 H); 7.08-7.00 (m, 2 H); 6.92-6.85 (m, 3 H); 6.77 (d, J = 8.40 Hz, 1 H); 6.49 (d, J = 9.86 Hz, 1 H); 5.75 (d, J = 9.21 Hz, 1 H); 5.00 (dd, J = 7.96, 4.49 Hz, 1 H); 4.55 (s, 1 H); 3.94-3.87 (m, 2 H); 3.07 (t, J = 10.34 Hz, 1 H); 2.74-2.60 (m, 6 H); 2.26 (s, 3 H); 1.88 (s, 1 H); 1.78 (s, 1 H); 1.73-1.61 (m, 2 H); 1.56 (s, 1 H); 1.31 (d, J = 46.94 Hz, 17 H) none 19 A (DMSO-d6): δ 8.21-8.10 (m, 2 H); 7.23-7.15 (m, 3 H); 7.11 (d, J = 7.79 Hz, 2 H); 7.05 (d, J = 8.15 Hz, 1 H); 6.92-6.84 (m, 3 H); 6.77 (d, J = 8.32 Hz, 1 H); 6.49 (d, J = 9.86 Hz, 1 H); 5.76 (d, J = 9.15 Hz, 1 H); 5.00 (dd, J = 7.91, 4.48 Hz, 1 H); 4.55 (s, 1 H); 3.94-3.87 (m, 2 H); 3.06 (s, 1 H); 2.73-2.60 (m, 6 H); 2.25 (s, 3 H); 1.88 (s, 1 H); 1.78 (s, 1 H); 1.73- 1.61 (m, 2 H); 1.56 (s, 1 H); 1.57-1.14 (m, 17 H). none B (DMSO-d6): δ 8.31 (s, 2 H); 8.27-8.15 (m, 2 H); 7.41-7.31 (m, 2 H); 7.24-7.07 (m, 4 H); 6.98-6.84 (m, 3 H); 6.81-6.75 (m, 1 H); 6.53 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.3 Hz, 1 H); 5.22-5.16 (m, 1 H); 4.62-4.54 (m, 1 H); 3.91 (t, J = 6.5 Hz, 2 H); 3.15- 3.06 (m, 1 H); 2.92-2.81 (m, 2 H); 2.80-2.45 (m, 4 H); 1.94-1.20 (m, 22 H). diformate 1B A (DMSO-d6): δ 8.25 (d, J = 9.8 Hz, 1 H); 8.17 (d, J = 9.9 Hz, 1 H); 7.40-7.32 (m, 1 H); 7.25-7.15 (m, 3 H); 7.09-7.02 (m, 2 H); 6.96-6.87 (m, 3 H); 6.82-6.77 (m, 1 H); 6.49 (d, J = 9.9 Hz, 1 H); 5.84 (d, J = 9.0 Hz, 1 H); 5.00 (dd, J = 7.9, 4.5 Hz, 1 H); 4.60-4.53 (m, 1 H); 3.92 (t, J = 6.5 Hz, 2 H); 3.12-3.02 (m, 1 H); 2.77-2.53 (m, 6H); 1.92-1.20 (m, 22 H) none 2B B (DMSO-d6): δ 8.33-8.26 (m, 3 H); 8.18 (d, J = 9.9 Hz, 1 H); 7.42 (s, 1 H); 7.38-7.27 (m, 3 H); 7.22 (t, J = 8.0 Hz, 1 H); 7.10 (d, J = 8.2 Hz, 1 H); 6.98-6.87 (m, 3 H); 6.82-6.77 (m, 1 H); 6.53 (d, J = 9.9 Hz, 1 H); 5.84 (d, J = 9.2 Hz, 1 H); 5.18 (dd, J = 8.0, 4.6 Hz, 1 H); 4.62-4.55 (m, 1 H); 3.92 (t, J = 6.6 Hz, 2 H); 3.16-3.06 (m, 1 H); 2.90-2.83 (m, 2 H); 2.80-2.52 (m, 6 H); 1.94-1.22 (m, 20 H). diformate 1C C (DMSO-d6 @105°C): δ 8.21-8.10 (m, 3 H); 7.19-7.11 (m, 1 H); 7.06 (d, J = 8.2 Hz, 1 H); 6.97-6.89 (m, 2 H); 6.86-6.77 (m, 2 H); 6.74 (d, J = 8.2 Hz, 1 H); 6.46 (d, J = 9.9 Hz, 1 H); 5.04-4.96 (m, 1 H); 4.55-4.47 (m, 1 H); 4.28-4.18 (m, 1 H); 3.99-3.89 (m, 2 H); 3.07-2.97 (m, 1 H); 2.81-2.50 (m, 8 H); 1.88-0.79 (m, 31 H). diformate (continued) 181 2C C (DMSO-d6): δ 8.38 (d, J = 9.86 Hz, 1 H); 8.31 (s, 1 H); 8.19 (d, J = 9.93 Hz, 1 H); 7.41-7.38 (m, 1 H); 7.29-7.20 (m, 1 H); 7.11 (d, J = 8.16 Hz, 1 H); 7.02- 6.89 (m, 4 H); 6.87-6.79 (m, 2 H); 6.53 (d, J = 9.85 Hz, 1 H); 6.00 (d, J = 8.88 Hz, 1 H); 5.19 (dd, J = 8.24, 4.47 Hz, 1 H); 4.60 (s, 1 H); 3.97-3.90 (m, 2 H); 3.12 (d, J = 13.06 Hz, 1 H); 2.87 (d, J = 8.12 Hz, 2 H); 2.80-2.49 (m, 6 H); 1.99-1.86 (m, 1 H); 1.8-1.3 (m, 13 H). formate 3C B (DMSO-d6): δ 8.30 (s, 2 H); 8.26-8.15 (m, 2 H); 7.46 (dd, J = 5.00, 2.93 Hz, 1 H); 7.30 (s, 1 H); 7.26-7.18 (m, 1 H); 7.12 (d, J = 8.17 Hz, 1 H); 7.07-7.03 (m, 1 H); 6.94 (dd, J = 19.65, 8.17 Hz, 3 H); 6.79 (d, J = 8.29 Hz, 1 H); 6.54 (d, J = 9.85 Hz, 1 H); 5.86 (d, J = 8.02 Hz, 1 H); 5.23 (dd, J = 8.83, 3.83 Hz, 1 H); 4.60 (s, 1 H); 3.96-3.90 (m, 2 H); 3.14 (s, 1 H); 2.99-2.83 (m, 2 H); 2.87-2.44 (m, 6 H); 1.92 (s, 1 H); 1.80 (s, 1 H); 1.72-1.31 (m, 12 H). diformate 21 A (DMSO-d6): δ 8.20 (br s, 1H), 7.34-7.18 (m, 6H), 6.92-6.88 (m, 2H), 6.79 (d, J= 8.4 Hz, 1H), 6.68 (d, J = 8.4 Hz, 1H), 5.80 (br s, 1H), 4.57-4.55 (m, 1H), 3.93-3.90 (m, 2H), 3.10-3.05 (m, 1H), 2.72-2.68 (m, 3H), 2.60-2.50 (m, 8H), 1.88 (s, 1H), 1.71-1.67 (m, 2H), 1.64 (br s, 1H), 1.57-1.25 (m, 15H) none 22 A (DMSO-d6): δ 8.29-8.21 (m, 2 H); 8.18 (d, J = 9.9 Hz, 1 H); 7.37-7.27 (m, 6 H); 7.26-7.18 (m, 4 H); 7.09 (d, J = 8.2 Hz, 1 H); 7.01 (s, 1 H); 6.97-6.84 (m, 3 H); 6.52 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.3 Hz, 1 H); 5.12 (t, J = 6.3 Hz, 1 H); 5.02 (s, 2 H); 4.63-4.56 (m, 1 H); 3.19-3.09 (m, 1 H); 2.97-2.52 (m, 11 H); 1.96-1.74 (m, 2 H); 1.67-1.30 (m, 3 H). formate 23 B (DMSO-d6): δ 8.30-8.21 (m, 3 H); 8.17 (d, J = 9.9 Hz, 1 H); 7.35-7.13 (m, 8 H); 7.08 (d, J = 8.0 Hz, 2 H); 6.94 (d, J = 8.1 Hz, 1 H); 6.51 (d, J = 9.9 Hz, 1 H); .82 (d, J = 9.3 Hz, 1 H); 5.13 (t, J = 6.3 Hz, 1 H); 4.63-4.55 (m, 1 H); 3.18-3.09 (m, 1 H); 2.95-2.52 (m, 11 H); 1.96-1.75 (m, 2 H); 1.65-1.28 (m, 3 H). diformate 24 A (DMSO-d6): δ 8.60 (br d, J = 8.8 Hz, 1H), 8.48 (s, 1H), 8.18-8.16 (m, 1H), 7.99-7.97 (m, 2H), 7.75-7.74 (m, 1H), 7.63-7.58 (m, 2H), 7.37-7.32 (m, 4H), 7.27- 7.21 (m, 2H), 7.06-7.04 (m, 1H), 6.96-6.89 (m, 3H), 6.82-6.80 (m, 1H), 6.49-6.47 (m, 1H), 5.85 (br d, J = 8.8 Hz, 1H), 5.20 (br s, 2H), 5.04 (br m, 2H), 4.08 (m, 1H), 3.92 (t, J = 6 Hz, 2H), 3.75-3.69 (m, 3H), 3.44 (m, 2H), 2.72-2.67 (m, 2H), 2.56-2.51 (m, 2H), 2.34-2.33 (m, 1H), 2.20 (m, 1H), 2.09-1.98 (m, 3H), 1.69-1.66 (m, 2H), 1.44-1.30 (m, 6H) formate (continued) 182 3B A (DMSO-d6): δ 8.30-8.22 (m, 2 H); 8.18 (d, J = 9.9 Hz, 1 H); 7.38-7.14 (m, 10 H); 7.10-7.00 (m, 2 H); 6.97-6.86 (m, 3 H); 6.51 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 8.8 Hz, 1 H); 5.10 (t, J = 6.3 Hz, 1 H); 5.02 (s, 2 H); 4.62-4.54 (m, 1 H); 3.17-3.07 (m, 1 H); 2.95-2.52 (m, 11 H); 1.95-1.74 (m, 2 H); 1.66-1.28 (m, 3 H). formate 4B B (DMSO-d6): δ 8.58 (dd, J = 9.2, 4.7 Hz, 1 H); 8.40 (s, 2 H); 8.17 (dd, J = 9.9, 1.7 Hz, 1 H); 7.97 (t, J = 7.5 Hz, 2 H); 7.75 (q, J = 6.8 Hz, 1 H); 7.60 (q, J = 8.0 Hz, 2 H); 7.40-7.16 (m, 10 H); 7.07-7.00 (m, 2 H); 6.97-6.87 (m, 3 H); 6.49 (dd, J = 9.9, 1.8 Hz, 1 H); 5.87-5.82 (m, 1 H); 5.22-5.14 (m, 2 H); 5.07- 4.99 (m, 4 H); 4.13-4.04 (m, 1 H); 3.79-3.53 (m, 5 H); 2.85-2.66 (m, 6 H); 2.38-2.31 (m, 1 H); 2.24- 2.13 (m, 1 H); 2.10-1.91 (m, 3 H). diformate 5B A (DMSO-d6): δ 8.61 (d, J = 9.2 Hz, 1 H); 8.42 (s, 2 H); 8.18 (d, J = 9.9 Hz, 1 H); 8.02-7.94 (m, 2 H); 7.79-7.71 (m, 1 H); 7.65-7.57 (m, 2 H); 7.44 (d, J = .5 Hz, 1 H); 7.40-7.29 (m, 3 H); 7.28-7.21 (m, 1 H); 7.06 (d, J = 8.1 Hz, 1 H); 6.99-6.89 (m, 3 H); 6.83 (d, J = 8.3 Hz, 1 H); 6.49 (d, J = 9.8 Hz, 1 H); .87 (d, J = 8.4 Hz, 1 H); 5.24-5.13 (m, 2 H); 5.11- .00 (m, 2 H); 4.14-4.02 (m, 1 H); 3.93 (t, J = 7.1 Hz, 2 H); 3.80-3.65 (m, 4 H); 2.79-2.66 (m, 2 H); 2.65-2.54 (m, 2 H); 2.39-2.31 (m, 1 H); 2.24-2.12 (m, 1 H); 2.11-1.91 (m, 3 H); 1.73-1.62 (m, 2 H); 1.48-1.18 (m, 13 H). diformate 6B A (DMSO-d6): δ 8.59 (d, J = 8.87 Hz, 1 H); 8.43 (s, 2 H); 8.18 (d, J = 9.89 Hz, 1 H); 7.98 (d, J = 7.80 Hz, 2 H); 7.79-7.71 (m, 1 H); 7.65-7.57 (m, 2 H); 7.39-7.33 (m, 4 H); 7.27 (dd, J = 8.36, 5.16 Hz, 1 H); 7.15 (d, J = 10.12 Hz, 1 H); 7.09-7.01 (m, 2 H); 7.01-6.91 (m, 2 H); 6.49 (dd, J = 9.85, 1.23 Hz, 1 H); 5.86 (d, J = 8.44 Hz, 1 H); 5.19 (s, 2 H); 5.04 (d, J = 7.00 Hz, 2 H); 4.14-4.04 (m, 1 H); 3.98-3.91 (m, 2 H); 3.7-3.5 (m, 4 H); 2.74-2.64 (m, 2 H); 2.56 (d, J = 10.06 Hz, 2 H); 2.38-2.31 (m, 2 H); 2.19 (d, J = 17.51 Hz, 1 H); 2.09- 1.92 (m, 3 H); 1.66 (d, J = 8.03 Hz, 2 H); 1.32 (d, J = 52.59 Hz, 12 H). diformate 7B B (DMSO-d6): δ 8.32 (s, 1 H); 8.27 (d, J = 9.28 Hz, 1 H); 8.18 (d, J = 9.93 Hz, 1 H); 7.35-7.21 (m, 6 H); 7.15-7.03 (m, 3 H); 6.95 (d, J = 8.13 Hz, 1 H); 6.53 (d, J = 9.86 Hz, 1 H); 6.23 (d, J = 8.86 Hz, 1 H); .18 (dd, J = 8.02, 4.59 Hz, 1 H); 4.56 (s, 1 H); 4.06- 3.99 (m, 2 H); 3.14-3.03 (m, 1 H); 2.86 (d, J = 7.36 Hz, 2 H); 2.79-2.53 (m, 6 H); 1.94-1.85 (m, 1 H); 1.79-1.68 (m, 3 H); 1.76-1.13 (m, 16 H). formate (continued) 183 8B A (DMSO-d6): δ 8.32 (s, 1 H); 8.22-8.11 (m, 2 H); 7.35-7.24 (m, 5 H); 7.16-7.07 (m, 2 H); 7.06-6.96 (m, 1 H); 6.95 (d, J = 8.13 Hz, 1 H); 6.53 (d, J = 9.86 Hz, 1 H); 6.23 (d, J = 8.18 Hz, 1 H); 5.20- .14 (m, 1 H); 4.59 (s, 1 H); 4.02-3.95 (m, 2 H); 3.14-3.04 (m, 1 H); 2.88-2.83 (m, 2 H); 2.78-2.53 (m, 6 H); 1.99-1.77 (m, 2 H); 1.72-1.63 (m, 2 H); 1.73-1.12 (m, 16 H). formate 9B A (DMSO-d6): δ 8.34-8.24 (m, 3 H); 8.18 (d, J = 9.9 Hz, 1 H); 7.51-7.43 (m, 1 H); 7.37-7.19 (m, 5 H); 7.18-7.07 (m, 2 H); 6.96 (d, J = 8.1 Hz, 1 H); 6.83 (dd, J = 8.8, 2.9 Hz, 1 H); 6.53 (d, J = 9.9 Hz, 1 H); 6.16-6.07 (m, 1 H); 5.20 (dd, J = 8.4, 4.3 Hz, 1 H); 4.63-4.54 (m, 1 H); 3.94 (t, J = 6.5 Hz, 2 H); 3.19-3.04 (m, 1 H); 2.93-2.82 (m, 2 H); 2.81- 2.53 (m, 6 H); 1.97-1.86 (m, 1 H); 1.85-1.08 (m, 19 H). diformate 10B B (DMSO-d6): δ 8.59 (dd, J = 8.88, 3.56 Hz, 1 H); 8.43 (s, 2 H); 8.18 (d, J = 9.92 Hz, 1 H); 8.01- 7.94 (m, 2 H); 7.79-7.72 (m, 1 H); 7.61 (q, J = 6.64 Hz, 2 H); 7.39-7.21 (m, 6 H); 7.15-7.02 (m, 3 H); 6.95 (d, J = 8.10 Hz, 1 H); 6.49 (d, J = 9.83 Hz, 1 H); 6.28-6.20 (m, 1 H); 5.20 (d, J = 7.19 Hz, 2 H); 5.07-5.00 (m, 2 H); 4.09-4.00 (m, 3 H); 3.80-3.56 (m, 4 H); 2.72 (d, J = 7.37 Hz, 2 H); 2.6 (m, 2 H); 2.34 (m, 2 H); 2.2-1.9 (m, 4 H); 1.72 (d, J = 8.43 Hz, 2 H); 1.27 (t, J = 51.58 Hz, 12 H). diformate 11B A (DMSO-d6): δ 8.54-8.45 (m, 1 H); 8.42 (s, 2 H); 8.17 (d, J = 9.92 Hz, 1 H); 8.01-7.90 (m, 2 H); 7.75 (dd, J = 14.66, 7.33 Hz, 1 H); 7.67-7.56 (m, 2 H); 7.41-7.27 (m, 5 H); 7.19-7.10 (m, 1 H); 7.08-6.99 (m, 2 H); 6.95 (t, J = 7.26 Hz, 1 H); 6.49 (d, J = 9.84 Hz, 1 H); 6.25 (dd, J = 14.03, 8.15 Hz, 1 H); 5.19 (d, J = 12.14 Hz, 2 H); 5.05 (s, 2 H); 4.09 (dd, J = 13.40, 8.00 Hz, 1 H); 4.03- 3.96 (m, 2 H); 3.83-3.50 (m, 4 H); 2.74-2.66 (m, 2 H); 2.6 (m, 2 H); 2.39- 2.22 (m, 3 H); 2.11-1.91 (m, 3 H); 1.69 (d, J = 7.79 Hz, 2 H); 1.32 (d, J = 55.24 Hz, 12 H). diformate (continued) 184 12B B (DMSO-d6): δ 8.67-8.58 (m, 1 H); 8.43 (s, 2 H); 8.18 (d, J = 9.9 Hz, 1 H); 8.02-7.93 (m, 2 H); 7.75 (q, J = 7.1 Hz, 1 H); 7.61 (q, J = 7.8 Hz, 2 H); 7.50 (d, J = 8.7 Hz, 1 H); 7.40-7.22 (m, 5 H); 7.14 (dd, J = 19.7, 3.0 Hz, 1 H); 7.06 (d, J = 8.2 Hz, 1 H); 6.95 (d, J = 8.1 Hz, 1 H); 6.85 (dd, J = 8.8, 2.9 Hz, 1 H); 6.49 (d, J = 9.8 Hz, 1 H); 6.21-6.11 (m, 1 H); 5.20 (d, J = 8.9 Hz, 2 H); 5.10-5.00 (m, 2 H); 4.14-4.04 (m, 1 H); 4.01-3.89 (m, 2 H); 3.81-3.51 (m, 5 H); 2.78-2.66 (m, 2 H); 2.63-2.53 (m, 2 H); 2.40-2.30 (m, 1 H); 2.23- 1.90 (m, 4 H); 1.74-1.64 (m, 2 H); 1.47-1.17 (m, 12 H). diformate 13B A (DMSO-d6): δ 8.51 (d, J = 9.58 Hz, 1 H); 8.43 (s, 2 H); 8.17 (d, J = 9.96 Hz, 1 H); 8.01-7.95 (m, 2 H); 7.80-7.72 (m, 1 H); 7.64-7.57 (m, 2 H); 7.36-7.30 (m, 4 H); 7.26- 7.21 (m, 1 H); 7.08-7.04 (m, 2 H); 6.94 (d, J = 8.15 Hz, 2 H); 6.85-6.79 (m, 1 H); 6.49 (d, J = 9.86 Hz, 1 H); .81 (d, J = 8.39 Hz, 1 H); 5.19 (s, 2 H); 5.06-5.01 (m, 2 H); 4.08 (s, 1 H); 3.93 (d, J = 8.29 Hz, 2 H); 3.81-3.53 (m, 4 H); 2.72-2.65 (m, 2 H); 2.6-2.5 (m, 2 H); 2.34 (t, J = 3.03 Hz, 2 H); 2.20-1.95 (m, 7 H); 1.74-1.66 (m, 2 H); 1.33 (d, J = 57.30 Hz, 12 H). diformate 14B B (CD3OD): δ 8.45 (s, 2H), 8.40 (d, J = 10Hz, 1H); 7.36-7.27 (m, 6H); 7.06 (d, J = 8.4 Hz, 1H); 6.93 (d, J = 8 Hz, 1H); 6.86-6.83 (m, 2H); 6.72 (d, J = 9.6 Hz, 1H); 5.85 (br s, 1H); 5.42 (t, J = 6.8 Hz, 1H); 5.01- 4.99 (m, 1H); 3.93 (t, J = 6.4 Hz, 2H); 3.83 (s, 3H); 3.70 (m, 1H), 3.27-3.15 (m, 6H); 3.10-3.06 (m, 2H); 2.37 (br s, 1H); 2.24 (br s, 1H); 2.05 (m, 1H); 1.95- 1.86 (m, 2H); 1.77 -1.72 (m, 4H); 1.47-1.39 (m, 11H) diformate 15B B (DMSO-d6): δ 8.32 (s, 1 H); 8.18 (m, 2 H); 7.35-7.27 (m, 4 H); 7.26-7.20 (m, 1 H); 7.10 (d, J = 8.16 Hz, 1 H); 6.99-6.91 (m, 1 H); 6.56-6.50 (m, 3 H); 6.34 (s, 1 H); .76 (d, J = 8.94 Hz, 1 H); 5.18 (dd, J = 8.05, 4.61 Hz, 1 H); 4.58 (s, 1 H); 3.93-3.87 (m, 2 H); 3.70 (d, J = 1.68 Hz, 3 H); 3.11 (d, J = 12.65 Hz, 1 H); 2.89-2.82 (m, 2 H); 2.74-2.5 (m, 6 H); 1.91 (s, 1 H); 1.81 (s, 1 H); 1.75- 1.42 (m, 6 H); 1.67-0.96 (m, 12 H). formate 16B A (CD3OD): δ 8.57 (s, 2 H); 8.39 (d, J = 9.8 Hz, 1 H); 8.01 (d, J = 7.8 Hz, 2 H); 7.78-7.70 (m, 1 H); 7.62- 7.55 (m, 2 H); 7.38-7.26 (m, 6 H); 7.03 (d, J = 8.2 Hz, 1 H); 6.93 (d, J = 8.2 Hz, 1 H); 6.90-6.81 (m, 2 H); 6.69 (dd, J = 9.8, 1.3 Hz, 1 H); 5.87 (s, 1 H); 5.41- .34 (m, 1 H); 5.14 (s, 1 H); 4.23-4.13 (m, 1 H): 3.95- 3.70 (m, 10 H); 3.20-3.14 (m, 2 H); 3.04-2.97 (m, 2 H); 2.50 (s, 1 H); 2.45-2.34 (m, 1 H); 2.27-2.17 (m, 1 H); 2.15-2.03 (m, 2 H); 1.77-1.69 (m, 5 H); 1.47-1.39 (s, 11 H) diformate (continued) 185 17B B (DMSO-d6): δ 8.55-8.48 (m, 1 H); 8.41 (s, 2 H); 8.18 (d, J = 9.92 Hz, 1 H); 8.01-7.95 (m, 2 H); 7.79-7.71 (m, 1 H); 7.64-7.57 (m, 2 H); 7.38-7.29 (m, 4 H); 7.27-7.22 (m, 1 H); 7.07 (d, J = 8.15 Hz, 1 H); 6.96 (d, J = 8.11 Hz, 1 H); 6.57-6.46 (m, 3 H); 6.37 (s, 1 H); 5.78 (d, J = 8.97 Hz, 1 H); .20 (s, 2 H); 5.13-5.06 (m, 1 H); 5.03 (s, 1 H); 4.14-4.03 (m, 1 H); 3.94-3.87 (m, 2 H); 3.71 (d, J = 2.10 Hz, 5 H); 3.60 (s, 2 H); 2.75 (d, J = 6.24 Hz, 2 H); 2.59 (d, J = 10.43 Hz, 2 H); 2.35 (d, J = 6.09 Hz, 1 H); 2.25-1.92 (m, 4 H); 1.71-1.62 (m, 2 H); 1.54-1.16 (m, 13 H). diformate 18B B (DMSO-d6): δ 8.65-8.58 (m, 1 H); 8.42 (s, 2 H); 8.18 (d, J = 9.89 Hz, 1 H); 7.97 (dd, J = 12.34, 7.73 Hz, 2 H); 7.77-7.70 (m, 1 H); 7.68-7.56 (m, 4 H); 7.48-7.29 (m, 7 H); 7.26 (d, J = 9.96 Hz, 2 H); 7.06 (d, J = 7.09 Hz, 2 H); 6.99 (s, 1 H); 6.94 (d, J = 8.20 Hz, 1 H); 6.52-6.48 (m, 1 H); 5.92 (d, J = 8.66 Hz, 1 H); 5.19 (d, J = 7.20 Hz, 2 H); 5.05 (d, J = 6.31 Hz, 2 H); 4.11-3.98 (m, 3 H); 3.82- 3.53 (m, 6 H); 2.74-2.66 (m, 2 H); 2.39-2.31 (m, 2 H); 2.22-1.89 (m, 4 H); 1.75-1.67 (m, 2 H); 1.33 (d, J = 56.95 Hz, 12 H). diformate 19B B (CD3OD): δ 8.57 (s, 2 H); 8.38 (d, J = 9.86 Hz, 1 H); 7.39-7.25 (m, 8 H); 7.17 (s, 1 H); 7.11-6.99 (m, 3 H); 6.76 (s, 1 H); 6.68 (dd, J = 9.83, 6.22 Hz, 1 H); 5.91 (s, 1 H); 5.35 (dd, J = 8.74, 4.54 Hz, 1 H); 4.81 (s, 1 H); 4.03-3.96 (m, 2 H); 3.18- 3.07 (m, 2 H); 3.02-2.82 (m, 7 H); 2.09 (d, J = 36.56 Hz, 2 H); 1.90-1.62 (m, 6 H); 1.64-1.23 (m, 12 H). diformate 20B B (CD3OD): δ 8.56 (s, 1 H); 8.39 (d, J = 10 Hz, 1 H); 8.02-7.98 (m, 2 H); 7.73 (m, 1 H); 7.61-7.55 (m, 2 H); 7.36-7.24 (m, 8 H); 7.04-6.87 (m, 7 H); 6.69 (d, J = 12 Hz, 1 H); 5.90 (s, 1 H); 5.39 (m, 1 H); 5.14-4.90 (m, 6 H); 4.26-3.71 (m, 8 H); 3.18- 3.11 (m, 4 H); 2.50-1.90 (m, 8 H) formate 21B A (DMSO-d6): δ 8.57 (m, 1 H); 8.45 (s, 2 H); 8.24 (d, J = 12 Hz, 1 H); 7.38-7.23 (m, 10 H); 7.13- 6.92 (m, 12 H); 6.54 (d, J = 8 Hz, 1 H); 5.89 (d, J = 8 Hz, 1 H); 5.16 (m, 1 H); 5.08 (s, 2 H); 4.98 (m, 1 H); 4.47 (m, 2 H); 4.08-4.00 (m, 3 H); 3.76- 3.40 (m, 5 H); 2.84 (m, 2 H); 2.75 (m, 2 H); 2.36 (m, 1 H); 2.19 (m, 1 H); 2.03-1.93 (m, 3 H); 1.77 (m, 2 H); 1.66 (m, 2 H) diformate (continued) 186 22B B (CD3OD): δ 8.56 (s, 1 H); 8.39 (d, J = 10 Hz, 1 H); 8.02-7.98 (m, 2 H); 7.73 (m, 1 H); 7.61-7.57 (m, 2 H); 7.36-7.23 (m, 8 H); 7.05-6.85 (m, 7 H); 6.69 (d, J = 10 Hz, 1 H); 5.90 (s, 1 H); 5.40 (t, J = 5.6 Hz, 1 H); 5.18-4.90 (m, 6 H); 4.18 (m, 1 H); 4.04-3.99 (m, 2 H); 3.85-3.60 (m, 5 H); 3.21-3.09 (m, 2 H); 3.10- 3.06 (m, 2 H); 2.68-2.00 (m, 5 H); 1.85-1.79 (m, 3 H); 1.62-1.61 (m, 2 H) formate 23B B (DMSO-d6): δ 8.58 (m, 1 H); 8.47 (s, 2 H); 8.24 (d, J = 12 Hz, 1 H); 7.38-7.23 (m, 10 H); 7.13-6.92 (m, 12 H); 6.53 (d, J = 12 Hz, 1 H); 5.89 (d, J = 8 Hz, 1 H); 5.16 (m, 1 H); 5.08 (s, 2 H); 4.98 (m, 1 H); 4.47 (m, 2 H); 4.08-3.97 (m, 3 H); 3.93-3.37 (m, 5 H); 2.83 (m, 2 H); 2.71 (m, 2 H); 2.34 (m, 1 H); 2.19 (m, 1 H); 2.03-1.85 (m, 3 H); 1.76 (m, 2 H); 1.53-1.47 (m, 4 H) diformate 24B A (DMSO-d6): δ 8.29 (s, 3 H); 8.19 (d, J = 9.92 Hz, 1 H); 7.39-7.32 (m, 1 H); 7.21 (d, J = 9.99 Hz, 3 H); 7.15-7.02 (m, 2 H); 6.94 (dd, J = 19.08, 8.27 Hz, 3 H); 6.80 (d, J = 8.28 Hz, 1 H); 6.54 (d, J = 9.85 Hz, 1 H); 5.85 (d, J = 8.92 Hz, 1 H); 5.24 (dd, J = 8.95, 3.71 Hz, 1 H); 4.61 (s, 1 H); 3.96-3.89 (m, 2 H); 3.20-3.10 (m, 1 H); 3.0-2.9 (m, 2H); 2.85-2.5 (m, 6 H); 1.93 (s, 1 H); 1.81 (s, 1 H); 1.72-1.32 (m, 12 H). diformate 25B A (CD3OD): δ 8.55 (s, 2 H); 8.38 (d, J = 10 Hz, 1 H); 7.37-7.18 (m, 13 H); 7.04-6.76 (m, 3 H); 6.69 (m, 1 H); 5.88 (s, 1 H); 5.40-5.36 (m, 1 H); 5.11-4.97 (m, 1 H); 4.00-3.95 (m, 2 H); 3.88-3.77 (m, 1 H); 3.22- 3.01 (m, 9 H); 2.78-2.65 (m, 2 H); 2.42 (br s, 1 H); 2.31 (br s, 1 H); 2.19-1.88 (m, 3 H); 1.87-1.58 (m, 12 H). diformate 26B B (DMSO-d6): δ 8.34-8.21 (m, 2 H); 8.17 (d, J = 9.9 Hz, 1 H); 7.40-7.13 (m, 9 H); 7.11-7.00 (m, 3 H); 6.98-6.86 (m, 3 H); 6.50 (d, J = 9.9 Hz, 1 H); 5.85 (d, J = 8.7 Hz, 1 H); 5.10 (t, J = 6.3 Hz, 1 H); 5.02 (s, 2 H); 4.67-4.51 (m, 1 H); 3.17-3.07 (m, 1 H); 2.95-2.53 (m, 8 H); 1.98-1.84 (m, 1 H); 1.81-1.74 (m, 2 H); 1.73-1.20 (m, 4 H). formate 27B A (DMSO-d6): δ 8.62 (d, J = 9.36 Hz, 1 H); 8.39 (s, 2 H); 8.17 (dd, J = 9.92, 2.70 Hz, 1 H); 8.00-7.90 (m, 2 H); 7.74 (q, J = 6.56 Hz, 1 H); 7.65-7.50 (m, 3 H); 7.37 (q, J = 7.36 Hz, 1 H); 7.30-7.12 (m, 7 H); 7.11-7.00 (m, 3 H); 6.98-6.87 (m, 3 H); 6.48 (dd, J = 9.87, 2.28 Hz, 1 H); 5.88 (d, J = 7.77 Hz, 1 H); 5.19 (s, 2 H); 5.03 (s, 4 H); 4.11-3.98 (m, 1 H); 3.65 (d, J = 55.36 Hz, 3 H); 2.85-2.66 (m, 2 H); 2.39-2.26 (m, 5 H); 2.33-2.03 (m, 1 H); 2.07-1.87 (m, 4 H). diformate (continued) 187 28B A (DMSO-d6): δ 8.40 (m, 1 H); 8.18 (s, 2 H); 7.92 (dd, J = 12.0, 8.0 Hz, 1 H); 7.82-7.77 (m, 2 H); 7.57 (m, 1 H); 7.46-7.39 (m, 2 H); 7.20-7.15 (m, 7 H); 7.09-7.03 (m, 2 H); 6.89-6.85 (m, 2 H); 6.77-6.72 (m, 3 H); 6.29 (dd, J = 12.0, 8.0 Hz, 1H); 5.67 (d, J = 8.0 Hz, 1 H); 5.02 (m, 2 H); 4.87 (m, 4 H); 3.92 (m, 1 H); 3.68-3.52 (m, 6 H); 3.42 (m, 1 H); 2.49 (m, 2 H); 2.17 (m, 1 H); 2.00 (m, 1 H); 1.89-1.53 (m, 3 H) diformate 29B B (DMSO-d6): δ 8.30 (s, 2 H); 8.30-8.15 (m, 2 H); 7.70 (s, 1 H); 7.63-7.54 (m, 3 H); 7.50-7.37 (m, 2 H); 7.32-7.17 (m, 8 H); 7.12-7.04 (m, 2 H); 6.98- 6.88 (m, 3 H); 6.52 (d, J = 9.9 Hz, 1 H); 5.83 (d, J = 9.2 Hz, 1 H); 5.21-5.05 (m, 3 H); 4.59 (s, 1 H); 3.15-3.10 (m, 1 H); 2.97-2.53 (m, 11 H); 1.92 (s, 1 H); 1.80 (s, 1 H); 1.72-1.24 (m, 3 H). diformate 30B B (DMSO-d6): δ 8.54-8.46 (m, 1 H); 8.31-8.21 (m, 2 H); 8.18 (d, J = 9.94 Hz, 1 H); 7.84 (d, J = 8.04 Hz, 2 H); 7.50 (d, J = 7.91 Hz, 2 H); 7.34-7.27 (m, 4 H); 7.26-7.19 (m, 2 H); 7.10 (d, J = 8.17 Hz, 1 H); 7.04 (s, 1 H); 6.98-6.85 (m, 3 H); 6.53 (d, J = 9.86 Hz, 1 H); 5.82 (d, J = 8.54 Hz, 1 H); .20 (dd, J = 8.25, 4.32 Hz, 1 H); 5.13 (s, 2 H); 4.59 (s, 1 H); 3.27 (m, 2 H); 3.12 (s, 1 H); 2.93- 2.63 (m, 6 H); 1.86 (d, J = 46.19 Hz, 2 H); 1.70- 1.22 (m, 10 H). formate 31B B (DMSO-d6): δ 8.62 (s, 1 H); 8.33-8.21 (m, 3 H); 8.19 (d, J = 9.93 Hz, 1 H); 7.85 (d, J = 7.99 Hz, 2 H); 7.50 (d, J = 7.90 Hz, 2 H); 7.35-7.19 (m, 6 H); 7.11 (d, J = 8.16 Hz, 1 H); 7.04 (s, 1 H); 6.99- 6.85 (m, 3 H); 6.52 (d, J = 9.86 Hz, 1 H); 5.82 (d, J = 8.75 Hz, 1 H); 5.21 (dd, J = 8.34, 4.26 Hz, 1 H); 5.13 (s, 2 H); 4.60 (s, 1 H); 3.32 (t, J = 6.31 Hz, 2 H); 2.95-2.75 (m, 5 H); 2.67 (s, 3 H); 2.57 (d, J = 16.50 Hz, 1 H); 1.94 (s, 1 H); 1.81 (t, J = 7.70 Hz, 3 H); 1.61 (s, 2 H); 1.51 (s, 2 H). diformate 32B A (DMSO-d6): 8.59-8.52 (m, 2 H); 8.40 (s, 2 H); 8.18 (m, 1 H); 7.97 (t, J = 8.2 Hz, 2 H); 7.84 (dd, J = 8.0, 2.1 Hz, 2 H); 7.77-7.71 (m, 1 H); 7.60 (q, J = 8.0 Hz, 2 H); 7.50 (d, J = 7.9 Hz, 2 H); 7.36- 7.30 (m, 4 H); 7.28-7.21 (m, 2 H); 7.06 (t, J = 8.4 Hz, 2 H); 6.99-6.88 (m, 3 H); 6.49 (m, 1 H); 5.84 (d, J = 9.0 Hz, 1 H); 5.24-4.96 (m, 6 H); 4.15- 4.03 (m, 1 H); 3.80-3.28 (m, 6 H); 2.75-2.63 (m, 4 H); 2.34 (s, 1 H); 2.23-1.89 (m, 5 H); 1.74-1.63 (m, 2 H) diformate (continued) 188 33B B (DMSO- d6): δ 8.33-8.18 (m, 2 H); 8.18 (d, J = 9.93 Hz, 1 H); 8.00-7.92 (m, 2 H); 7.57 (d, J = 7.95 Hz, 2 H); 7.35-7.21 (m, 6 H); 7.10 (d, J = 8.16 Hz, 1 H); 7.04 (s, 1 H); 6.95 (d, J = 8.04 Hz, 2 H); 6.89 (d, J = 8.33 Hz, 1 H); 6.52 (d, J = 9.86 Hz, 1 H); 5.82 (d, J = 8.71 Hz, 1 H); 5.18 (s, 3 H); 4.59 (s, 1 H); 4.32- 4.25 (m, 2 H); 3.18-3.08 (m, 1 H); 2.91-2.56 (m, 6 H); 1.92 (s, 1 H); 1.95-1.39 (m, 11 H). formate 34B A (DMSO- d6): δ 8.28 (s, 1 H); 8.24 (d, J = 9.6 Hz, 1 H); 8.19 (d, J = 10 Hz, 1 H); 7.96 (d, J = 8.0 Hz, 2 H); 7.57 (d, J = 7.9 Hz, 2 H); 7.31-7.22 (m, 6 H); 7.10-6.87 (m, 5 H); 6.53 (d, J = 10 Hz, 1 H); 5.83 (d, J = 8.8 Hz, 1 H); 5.18-5.11 (m, 3 H); 4.56 (br s, 1 H); 3.13-3.08 (m, 1 H); 2.85-2.61 (m, 8 H); 1.94- 1.86 (m, 1 H); 1.79-1.66 (m, 3 H), 1.63-1.24 (m, 10 H) formate 35B B (DMSO- d6): 8.31 (s, 1 H); 8.26-8.14 (m, 2H); 7.96 (d, J = 8 Hz, 2 H); 7.56 (d, J = 8 Hz, 2 H); 7.34-7.20 (m, 6 H); 7.13-7.00 (m, 2 H); 6.97-6.87 (m, 3 H); 6.53 (d, J = 9.6 Hz, 1 H); 5.82 (d, J = 8.96 Hz, 1 H); .23-5.08 (m, 3 H); 4.57 (s, 1 H); 4.28 (t, J = 6.44 Hz, 2 H); 3.16-3.03 (m, 1 H); 2.83-2.49 (m, 8 H); 1.94-1.26 (m, 14 H) formate 4C B (DMSO-d6): δ 8.29 (s, 2 H); 8.28-8.13 (m, 2 H); 7.96 (d, J = 7.9 Hz, 2 H); 7.57 (d, J = 7.9 Hz, 2 H); 7.34-7.19 (m, 6 H); 7.10 (d, J = 8.1 Hz, 1 H); 7.03 (s, 1 H); 6.92 (m, 3 H); 6.53 (d, J = 9.8 Hz, 1 H); .82 (d, J = 9.1 Hz, 1 H); 5.17 (s, 3 H); 4.57 (s, 1 H); 4.28 (t, J = 6.4 Hz, 2 H); 3.15-3.05 (m, 1 H); 2.85 (d, J = 6.4 Hz, 2 H); 2.73 (s, 5 H); 1.90 (s, 1 H); 1.85- 1.66 (m, 3 H); 1.51 (s, 4 H); 1.40 (s, 3 H); 1.32 (s, 6 H). diformate 5C B (DMSO-d6): δ 8.22 (s, 2 H); 8.12 (d, J = 9.9 Hz, 1 H); 7.99 (d, J = 7.9 Hz, 2 H); 7.57 (d, J = 7.9 Hz, 2 H); 7.45-7.33 (m, 4 H); 7.33-7.18 (m, 6 H); 7.10- 6.99 (m, 2 H); 6.96-6.85 (m, 3 H); 6.47 (d, J = 9.8 Hz, 1 H); 5.81 (d, J = 9.0 Hz, 1 H); 5.33 (s, 2 H); .18 (s, 2 H); 5.08 (dd, J = 7.6, 4.2 Hz, 1 H); 4.58 (s, 1 H); 3.79 (s, 2 H); 3.42 (s, 7 H); 3.13 (s, 2 H); 2.78- 2.62 (m, 3 H); 1.92 (s, 1 H). diformate 6C A (DMSO-d6): δ 8.38 (s, 2 H); 8.28-8.16 (m, 2 H); 8.13 (d, J = 7.9 Hz, 2 H); 7.65 (d, J = 7.9 Hz, 2 H); 7.36-6.86 (m, 15 H); 6.52 (d, J =10 Hz, 1 H); 5.87- .78 (m, 1 H); 5.23 (s, 2 H); 5.05 (m, 1 H); 4.57 (br s, 1 H); 3.14-3.04 (m, 1 H); 2.91-2.63 (m, 11 H); 1.90 (br s, 1 H); 1.77 (br s, 1 H); 1.58 (br s, 1 H); 1.47 (br s, 1 H); 1.32 (br s, 1 H). diformate (continued) 189 7C A (DMSO-d6): δ 8.32-8.19 (m, 2 H); 8.21-8.10 (m, 2 H); 8.02 (d, J = 8.0 Hz, 2 H); 7.58 (d, J = 7.9 Hz, 2 H); 7.37-7.16 (m, 6 H); 7.10 (d, J = 8.2 Hz, 1 H); 7.05 (s, 1 H); 6.92 (dd, J = 23.2, 8.0 Hz, 3 H); 6.53 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.1 Hz, 1 H); 5.22- .14 (m, 3 H); 4.70 (s, 2 H); 4.58 (s, 1 H); 3.17 (s, 1 H); 3.12 (d, J = 7.1 Hz, 3 H); 2.85 (d, J = 6.3 Hz, 2 H); 2.75 (s, 4 H); 2.65 (d, J = 20.1 Hz, 2 H); 1.92 (s, 1 H); 1.48 (s, 6 H); 1.35 (s, 2 H). formate 8C B (DMSO-d6): δ 8.27 (s, 2 H); 8.25-8.15 (m, 2 H); 7.99 (d, J = 8.0 Hz, 2 H); 7.57 (d, J = 8.0 Hz, 2 H); 7.38 (d, J = 7.9 Hz, 2 H); 7.34-7.18 (m, 8 H); 7.09- 7.00 (m, 2 H); 6.96-6.85 (m, 3 H); 6.52 (d, J = 10 Hz, 1 H); 5.82 (d, J = 9.2 Hz, 1 H); 5.32 (s, 2 H); .18 (s, 2 H); 5.07 (m, 1 H); 4.60–4.53 (m, 1 H); 3.15-3.05 (m, 1 H); 2.89-2.70 (m, 9 H); 1.89 (br s, 2 H); 1.78 (br s, 2 H); 1.59 (br s, 1 H); 1.46 (br s, 1 H); 1.31 (br s, 1 H) formate 36B B (DMSO-d6): δ 8.58 (d, J = 8.9 Hz, 1 H); 8.37 (s, 2 H); 8.18 (d, J = 9.9 Hz, 1 H); 7.97 (t, J = 6.6 Hz, 2 H); 7.78-7.71 (m, 1 H); 7.60 (q, J = 7.4 Hz, 2 H); 7.40-7.21 (m, 10 H); 7.10-6.99 (m, 2 H); 6.99-6.86 (m, 3 H); 6.50 (dd, J = 9.8, 1.6 Hz, 1 H); 5.85 (d, J = 8.3 Hz, 1 H); 5.22-5.14 (m, 2 H); 5.09 (t, J = 6.2 Hz, 1 H); 5.07-4.97 (m, 3 H); 4.13-4.04 (m, 1 H); 4.01- 3.94 (m, 2 H); 3.78-3.53 (m, 6 H); 2.72 (d, J = 6.1 Hz, 2 H); 2.62-2.53 (m, 1 H); 2.37-2.31 (m, 1 H); 2.24-2.13 (m, 1 H); 2.09-1.90 (m, 3 H); 1.55-1.33 (m, 6 H); 1.20-1.12 (m, 2 H). diformate 37B B (DMSO-d6 @105°C): δ 8.21-8.14 (m, 3 H); 7.63- 7.52 (m, 5 H); 7.41-7.18 (m, 10 H); 7.10 (d, J = 8.1 Hz, 1 H); 6.98-6.81 (m, 4 H); 6.46 (d, J = 9.9 Hz, 1 H); 5.83 (d, J = 8.8 Hz, 1 H); 5.09 (dd, J = 7.6, 4.8 Hz, 1 H); 4.64-4.58 (m, 1 H); 4.24 (td, J = 6.7, 2.0 Hz, 2 H); 3.82 (s, 2 H); 3.13-3.03 (m, 3 H); 2.90- 2.77 (m, 1 H); 2.76-2.58 (m, 4 H); 2.57-2.52 (m, 2 H); 1.94-1.88 (m, 1 H); 1.82-1.70 (m, 1 H); 1.66- 1.56 (m, 1 H); 1.54-1.43 (m, 1 H); 1.36-1.24 (m, 1 H). diformate 38B A (DMSO-d6): δ 8.29-8.20 (m, 2 H); 8.12 (d, J = 9.9 Hz, 1 H); 7.65-7.49 (m, 4 H); 7.44-7.18 (m, 10 H); 7.08 (d, J = 8.2 Hz, 1 H); 6.99-6.80 (m, 4 H); 6.42 (d, J = 9.9 Hz, 1 H); 5.85-5.78 (m, 1 H); 5.11 (dd, J = 7.7, 4.5 Hz, 1 H); 4.63-4.56 (m, 1 H); 4.22-4.14 (m, 2 H); 3.86 (s, 2 H); 3.18-3.02 (m, 3 H); 2.81- 2.53 (m, 5 H); 2.52-2.45 (m, 2 H); 1.95-1.73 (m, 2 H); 1.66-1.27 (m, 3 H). formate (continued) 190 39B B (DMSO-d6): δ 8.35 (s, 2 H); 8.26 (d, J = 9.9 Hz, 1 H); 8.20 (d, J = 9.9 Hz, 1 H); 7.35-7.27 (m, 4 H); 7.26-7.18 (m, 2 H); 7.11 (d, J = 8.2 Hz, 1 H); 6.99- 6.92 (m, 4 H); 6.80-6.73 (m, 1 H); 6.53 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.5 Hz, 1 H); 5.24-5.18 (m, 1 H); 4.75 (d, J = 1.9 Hz, 2 H); 4.74-4.44 (m, 1 H); 4.08 (t, J = 6.6 Hz, 2 H); 3.19-3.08 (m, 1 H); 2.93- 2.80 (m, 2 H); 2.81-2.60 (m, 6 H); 1.99-1.84 (m, 1 H); 1.91-1.70 (m, 1 H); 1.69-1.48 (m, 6 H); 1.48- 1.24 (m, 1 H); 1.53-0.98 (m, 4 H) diformate 40B A (DMSO-d6): δ 8.11 (s, 3 H); 8.02 (d, J = 9.9 Hz, 1 H); 7.22-7.05 (m, 4 H); 7.08-7.01 (m, 2 H); 6.95 (d, J = 8.2 Hz, 1 H); 6.81 (d, J = 8.2 Hz, 1 H); 6.76- 6.69 (m, 2 H); 6.62 (d, J = 8.3 Hz, 1 H); 6.38 (d, J = 9.8 Hz, 1 H); 5.63 (s, 1 H); 5.11 (d, J = 9.2 Hz, 1 H); 4.45 (s, 1 H); 3.75 (t, J = 6.4 Hz, 2 H); 3.06- 2.96 (m, 1 H); 2.85-2.39 (m, 9 H); 1.79 (s, 1 H); 1.66 (s, 1 H); 1.56-1.11 (m, 11 H) diformate 41B B (DMSO-d6): δ 8.30 (s, 1 H); 8.24 (d, J = 10.10 Hz, 1 H); 8.19 (d, J = 9.93 Hz, 1 H); 7.37-7.17 (m, 6 H); 7.11 (d, J = 8.17 Hz, 1 H); 7.00-6.86 (m, 3 H); 6.78 (dd, J = 8.26, 2.44 Hz, 1 H); 6.56-6.48 (m, 1 H); .81 (d, J = 8.52 Hz, 1 H); 5.20 (dd, J = 8.28, 4.46 Hz, 1 H); 4.58 (s, 1 H); 3.95-3.88 (m, 2 H); 3.18- 3.06 (m, 1 H); 2.86-2.55 (m, 8 H); 1.91 (s, 1 H); 1.80 (s, 1 H); 1.74-1.32 (m, 12 H). formate 42B A (DMSO-d6): δ 8.55 (d, J = 9.19 Hz, 1 H); 8.40 (s, 2 H); 8.19 (d, J = 9.91 Hz, 1 H); 7.98 (d, J = 7.80 Hz, 2 H); 7.76 (t, J = 7.40 Hz, 1 H); 7.61 (t, J = 7.67 Hz, 2 H); 7.40-7.30 (m, 4 H); 7.29-7.19 (m, 2 H); 7.07 (d, J = 8.17 Hz, 1 H); 6.99-6.86 (m, 3 H); 6.81 (d, J = 8.37 Hz, 1 H); 6.50 (d, J = 9.84 Hz, 1 H); 5.84 (d, J = 8.86 Hz, 1 H); 5.20 (s, 2 H); 5.09 (s, 1 H); 5.03 (s, 1 H); 4.14-4.03 (m, 1 H); 3.96-3.88 (m, 2 H); 3.82-3.55 (m, 6 H); 2.75 (s, 2 H); 2.64-2.57 (m, 2 H); 2.34 (d, J = 6.23 Hz, 1 H); 2.18 (s, 1 H); 2.13- 1.88 (m, 3 H); 1.67 (d, J = 8.37 Hz, 2 H); 1.51-1.21 (m, 5 H). diformate 43B A (CD3OD): δ 8.57 (s, 2H); 8.39 (d, J = 10 Hz, 1H); 8.02 (d, J = 9.6 Hz, 2 H); 7.75-7.70 (m, 1 H); 7.61- 7.55 (m, 2 H); 7.40-7.24 (m, 7 H); 7.03 (d, J = 8.2 Hz, 1 H); 6.94-6.80 (m, 3 H); 6.70 (d, J = 9.6 Hz, 1 H); 5.90 (s, 1 H); 5.40-5.36 (m, 1 H); 5.15 (br s, 1 H); 4.92 (s, 2 H); 4.22-4.15 (m, 1 H); 4.00-3.66 (m, 8 H); 3.19-3.12 (m, 2 H); 3.01 (t, J = 8 Hz, 2 H); 2.51 (s, 1 H); 2.45-2.33 (m, 1 H); 2.26-2.17 (m, 1 H); 2.15-2.00 (m, 1 H); 1.84-1.69 (m, 4 H); 1.58- 1.42 (m, 4 H) diformate (continued) 191 44B C (DMSO-d6): δ 8.34-8.22 (m, 3 H); 8.20 (d, J = 10 Hz, 1 H); 7.98 (d, J = 8.4 Hz, 2H); 7.58 (d, J = 8.4 Hz, 2 H); 7.38-7.20 (m, 6 H); 7.15-6.83 (m, 5 H); 6.54 (d, J = 9.6 Hz, 1 H); 5.82 (br s, 1 H); 5.24-5.13 (m, 3 H); 4.61-4.59 (m, 1 H); 4.31 (t, J = 6 Hz, 2 H); 3.21-3.09 (m, 1 H); 2.95-2.42 (m, 8 H); 1.95 (s, 1 H); 1.89-.29 (m, 9 H) diformate 45B B (DMSO-d6): δ 8.29 (s, 1 H); 8.24 (d, J = 9.71 Hz, 1 H); 8.18 (d, J = 9.94 Hz, 1 H); 7.97 (d, J = 8.07 Hz, 2 H); 7.57 (d, J = 8.01 Hz, 2 H); 7.32-7.18 (m, 6 H); 7.09 (d, J = 8.16 Hz, 1 H); 7.04 (s, 1 H); 6.94 (d, J = 8.01 Hz, 2 H); 6.89 (dd, J = 8.27, 2.55 Hz, 1 H); 6.51 (d, J = 9.86 Hz, 1 H); 5.82 (d, J = 9.09 Hz, 1 H); 5.20-5.12 (m, 3 H); 4.58 (s, 1 H); 4.29 (t, J = 6.28 Hz, 2 H); 3.10 (d, J = 10.66 Hz, 1 H); 2.87-2.52 (m, 8 H); 2.06-1.30 (m, 10 H). formate 9C A (DMSO-d6): δ 8.33 (s, 2 H); 8.27 (d, J = 9.9 Hz, 1 H); 8.19 (d, J = 9.9 Hz, 1 H); 7.35-7.27 (m, 4 H); 7.27-7.19 (m, 2 H); 7.11 (d, J = 8.2 Hz, 1 H); 6.99- 6.92 (m, 3 H); 6.79-6.74 (m, 1 H); 6.53 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.3 Hz, 1 H); 5.25-5.19 (m, 1 H); 4.75 (d, J = 2.0 Hz, 2 H); 4.80-4.37 (m, 1 H); 4.08 (t, J = 6.7 Hz, 2 H); 3.20-3.08 (m, 1 H); 2.92- 2.84 (m, 2 H); 2.79-2.70 (m, 4 H); 2.70-2.59 (m, 3 H); 1.99-1.86 (m, 1 H); 1.90-1.73 (m, 1 H); 1.62- 1.47 (m, 6 H); 1.43-1.20 (m, 3 H). diformate 10C B (DMSO-d6): δ 8.34 (s, 2 H); 8.29 (d, J = 10.0 Hz, 1 H); 8.19 (d, J = 9.9 Hz, 1 H); 7.35-7.27 (m, 4 H); 7.25-7.17 (m, 2 H); 7.10 (d, J = 8.2 Hz, 1 H); 6.99- 6.92 (m, 3 H); 6.81-6.74 (m, 1 H); 6.52 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.6 Hz, 1 H); 5.22-5.16 (m, 1 H); 4.75 (s, 2 H); 4.67-4.53 (m, 1 H); 4.13-4.06 (m, 2 H); 3.21-3.04 (m, 1 H); 2.87-2.80 (m, 2 H); 2.79- 2.46 (m, 7 H); 2.04-1.80 (m, 1 H); 1.95-1.68 (m, 1 H); 1.63-1.48 (m, 6 H); 1.63-1.12 (m, 1 H). diformate 11C B (DMSO-d6): δ 8.32-8.21 (m, 1 H); 8.24 (s, 2 H); 8.17 (d, J = 9.9 Hz, 1 H); 7.33-7.29 (m, 4 H); 7.27- 7.17 (m, 2 H); 7.11 (d, J = 8.2 Hz, 1 H); 6.99-6.91 (m, 2 H); 6.72 (s, 1 H); 6.61 (d, J = 8.2 Hz, 1 H); 6.54 (d, J = 9.9 Hz, 1 H); 5.79 (d, J = 9.0 Hz, 1 H); .21-5.15 (m, 1 H); 4.62-4.54 (m, 1 H); 4.00 (t, J = 6.4 Hz, 2 H); 3.22-3.02 (m, 1 H); 2.88-2.83 (m, 2 H); 2.80-2.71 (m, 2 H); 2.70-2.67 (m, 4 H); 1.93- 1.88 (m, 1 H); 1.81-1.80 (m, 1 H); 1.59-1.58 (m, 1 H); 1.65-1.35 (m, 12 H); 1.43-1.31 (m, 1 H); 1.24- 1.14 (m, 2 H) diformate (continued) 192 12C B (DMSO-d6): δ 8.31 (s, 2 H); 8.41-8.12 (m, 1 H); 8.17 (d, J = 9.9 Hz, 1 H); 7.41-7.21 (m, 4 H); 7.30-7.17 (m, 1 H); 7.18 (t, J = 8.1 Hz, 1 H); 7.09 (d, J = 8.2 Hz, 1 H); 6.95 (d, J = 8.3 Hz, 1 H); 6.99-6.83 (m, 1 H); 6.72 (s, 1 H); 6.61 (d, J = 8.1 Hz, 1 H); 6.51 (d, J = 9.8 Hz, 1 H); 5.79 (d, J = 9.0 Hz, 1 H); 5.23-5.06 (m, 1 H); 4.72-4.45 (m, 1 H); 4.01 (t, J = 6.4 Hz, 2 H); 3.25-2.98 (m, 1 H); 2.81-2.72 (m, 4 H); 2.83-2.46 (m, 4 H); 2.67- 2.45 (m, 1 H); 2.01-1.80 (m, 1 H); 1.94-1.67 (m, 1 H); 1.85-1.14 (m, 11 H); 1.57-1.13 (m, 2 H). diformate 13C C (CD3OD): δ 8.57 (s, 2 H); 8.37 (d, J = 9.8 Hz, 1 H); 7.34-7.20 (m, 7 H); 7.04 (d, J = 8.1 Hz, 1 H); 6.86 (s, 1 H); 6.82 (d, J = 8.1 Hz, 2 H); 6.69 (d, J = 9.8 Hz, 1 H); .83 (d, J = 7.2 Hz, 1 H); 5.38-5.32 (m, 1 H); 4.90-4.74 (m, 1 H); 4.24-3.99 (m, 2 H); 4.11-3.84 (m, 2 H); 3.41- 3.36 (m, 1 H); 3.10-3.03 (m, 3 H); 3.04-2.87 (m, 3 H); 2.92-2.58 (m, 2 H); 2.26-2.06 (m, 1 H); 2.25-1.90 (m, 1 H); 2.06-1.68 (m, 1 H); 1.79-1.67 (m, 1 H); 1.67-1.59 (m, 6 H); 1.69-0.95 (m, 8 H). diformate 14C A (DMSO-d6): δ 8.36 (s, 2 H); 8.28 (d, J = 9.9 Hz, 1 H); 8.20 (d, J = 9.9 Hz, 1 H); 7.35-7.27 (m, 4 H); 7.26-7.20 (m, 2 H); 7.11 (d, J = 8.2 Hz, 1 H); 6.97 (d, J = 8.1 Hz, 1 H); 7.00-6.85 (m, 2 H); 6.81-6.70 (m, 1 H); 6.53 (d, J = 9.8 Hz, 1 H); 5.81 (d, J = 9.2 Hz, 1 H); 5.26 (dd, J = 8.9, 3.8 Hz, 1 H); 4.77 (s, 2 H); 4.74-4.52 (m, 1 H); 4.15 (d, J = 12.9 Hz, 1 H); 4.19-3.91 (m, 2 H); 3.77 (d, J = 13.3 Hz, 1 H); 3.24-3.05 (m, 2 H); 2.97-2.88 (m, 2 H); 2.86-2.53 (m, 8 H); 2.09-1.85 (m, 1 H); 2.04-1.65 (m, 3 H); 1.93-1.23 (m, 8 H); 1.58-1.24 (m, 2 H). diformate 15C C (DMSO-d6): δ 8.31 (s, 2 H); 8.38-8.14 (m, 1 H); 8.18 (d, J = 9.9 Hz, 1 H); 7.34-7.15 (m, 9 H); 7.08 (d, J = 8.4 Hz, 1 H); 6.99-6.91 (m, 4 H); 6.82-6.75 (m, 1 H); 6.51 (d, J = 9.8 Hz, 1 H); 5.86-5.78 (m, 1 H); 5.28-4.95 (m, 3 H); 4.88-4.74 (m, 2 H); 4.70-4.49 (m, 1 H); 3.18- 3.06 (m, 1 H); 2.98-2.57 (m, 11 H); 2.01-1.80 (m, 1 H); 1.97-1.64 (m, 1 H); 1.76-1.44 (m, 1 H); 1.60-1.36 (m, 1 H); 1.56-1.16 (m, 1 H). diformate 16C A (DMSO-d6): δ 8.31 (s, 1 H); 8.24-8.14 (m, 2 H); 7.34- 7.26 (m, 4 H); 7.23-7.18 (m, 1 H); 7.10 (d, J = 8.16 Hz, 1 H); 7.04 (d, J = 7.67 Hz, 1 H); 6.95 (d, J = 8.10 Hz, 2 H); 6.82-6.76 (m, 1 H); 6.53 (d, J = 9.86 Hz, 1 H); 5.79 (d, J = 9.14 Hz, 1 H); 5.20-5.14 (m, 1 H); 4.58 (s, 1 H); 3.94-3.88 (m, 2 H); 3.17-3.05 (m, 1 H); 2.86-2.81 (m, 2 H); 2.8-2.6 (m, 6 H); 2.09 (s, 3 H); 1.91 (s, 1 H); 1.80 (s, 1 H); 1.75-1.64 (m, 2 H); 1.76-1.12 (m, 16 H). formate (continued) 193 17C A (DMSO-d6): δ 8.32 (s, 1 H); 8.28 (d, J = 8.85 Hz, 1 H); 8.18 (d, J = 9.93 Hz, 1 H); 7.36-7.30 (m, 4 H); 7.27-7.22 (m, 1 H); 7.15-7.06 (m, 2 H); 6.98 (d, J = 15.67 Hz, 3 H); 6.53 (d, J = 9.86 Hz, 1 H); .82 (d, J = 9.15 Hz, 1 H); 5.18 (dd, J = 7.97, 4.67 Hz, 1 H); 4.58 (s, 1 H); 3.97-3.91 (m, 2 H); 3.16- 3.05 (m, 1 H); 2.88-2.83 (m, 2 H); 2.80-2.53 (m, 7 H); 1.91 (s, 1 H); 1.80 (s, 1 H); 1.95-1.11 (m, 18 H). formate 18C B (DMSO-d6): δ 8.31 (s, 2 H); 8.18 (d, J = 9.92 Hz, 1 H); 7.66-7.62 (m, 2 H); 7.48-7.28 (m, 7 H); 7.27-7.19 (m, 2 H); 7.10 (d, J = 8.17 Hz, 1 H); 7.04 (s, 1 H); 6.95 (d, J = 7.85 Hz, 2 H); 6.53 (d, J = 9.86 Hz, 1 H); 5.89 (d, J = 8.99 Hz, 1 H); 5.20- .14 (m, 1 H); 4.59 (s, 1 H); 4.09-3.93 (m, 2 H); 3.12 (d, J = 13.08 Hz, 1 H); 2.87-2.82 (m, 2 H); 2.79-2.57 (m, 6 H); 1.92 (s, 1 H); 1.81 (s, 1 H); 1.75-1.67 (m, 2 H); 1.75-1.12 (m, 16 H). formate 19C A (DMSO-d6 @105°C): δ 8.23-8.13 (m, 3 H); 7.60- 7.49 (m, 1 H); 7.35-7.20 (m, 6 H); 7.15-7.05 (m, 2 H); 7.02-6.92 (m, 2 H); 6.51-6.45 (m, 1 H); 6.33-6.26 (m, 1 H); 5.06-5.00 (m, 1 H); 4.63-4.56 (m, 1 H); 4.10-4.01 (m, 2 H); 3.11-3.01 (m, 1 H); 2.84-2.52 (m, 8 H); 1.92-1.84 (m, 1 H); 1.82-1.54 (m, 4 H); 1.53-1.19 (m, 15 H). diformate 20C C (DMSO-d6): δ 8.28 (s, 2 H); 8.18 (d, J = 9.88 Hz, 1 H); 7.54-7.44 (m, 3 H); 7.39 (s, 2 H); 7.36-7.28 (m, 3 H); 7.24-7.15 (m, 2 H); 7.10 (d, J = 7.01 Hz, 2 H); 7.00 (s, 1 H); 6.95 (d, J = 8.23 Hz, 1 H); 6.53 (d, J = 9.86 Hz, 1 H); 5.89 (d, J = 8.77 Hz, 1 H); 5.16 (d, J = 7.81 Hz, 1 H); 4.59 (s, 1 H); 4.08- 3.96 (m, 2 H); 3.11 (s, 1 H); 2.94-2.76 (m, 2 H); 2.7-2.3 (m, 6 H); 1.92 (s, 1 H); 1.81 s, 1 H); 1.75- 1.66 (m, 2 H); 1.75-1.13 (m, 16 H). formate 21C C (CD3OD): δ 8.56 (s, 1 H); 8.38 (d, J = 9.9 Hz, 1 H); 7.33-7.20 (m, 8 H); 7.07-6.85 (m, 7 H); 6.70- 6.65 (m, 1 H); 5.87 (s, 1 H); 5.43-5.36 (m, 1 H); .03 (s, 2 H); 4.92 (m, 1H – obscured by water); 4.08-4.02 (m, 2 H); 3.51-3.50 (m, 1 H); 3.27-3.06 (m, 9 H); 2.30-1.60 (m, 9 H). formate 22C A (CD3OD): δ 8.56 (s, 1 H); 8.38 (d, J = 9.9 Hz, 1 H); 7.33-7.20 (m, 8 H); 7.07-6.85 (m, 7 H); 6.70- 6.65 (m, 1 H); 5.87 (s, 1 H); 5.43-5.36 (m, 1 H); .03 (s, 2 H); 4.92 (m, 1H – obscured by water); 4.08-4.02 (m, 2 H); 3.51-3.50 (m, 1 H); 3.27-3.06 (m, 9 H); 2.30-1.60 (m, 11 H). formate (continued) 194 23C C (DMSO-d6): δ 8.43 (s, 2 H); 8.19 (d, J = 9.9 Hz, 1 H); 8.03-7.88 (m, 3 H); 7.80-7.69 (m, 1 H); 7.68- 7.55 (m, 2 H); 7.20 (t, J = 7.9 Hz, 1 H); 7.06 (d, J = 8.2 Hz, 1 H); 6.96 (d, J = 8.1 Hz, 1 H); 6.92- 6.75 (m, 3 H); 6.49 (dd, J = 9.8, 1.3 Hz, 1 H); .25-5.06 (m, 3 H); 5.01-4.91 (m, 1 H); 4.26-4.00 (m, 2 H); 3.94 (t, J = 6.8 Hz, 2 H); 3.84-3.50 (m, H); 2.76 (d, J = 6.3 Hz, 2 H); 2.66-2.52 (m, 2 H); 2.38-1.78 (m, 6 H); 1.77-0.77 (m, 24 H). diformate 24C B (DMSO-d6): δ 8.75-8.66 (m, 1 H); 8.39 (s, 2 H); 8.19 (dd, J = 9.92, 1.99 Hz, 1 H); 8.02-7.93 (m, 2 H); 7.77-7.70 (m, 1 H); 7.61 (dd, J = 15.40, 7.70 Hz, 2 H); 7.44-7.41 (m, 1 H); 7.30-7.24 (m, 1 H); 7.10-6.92 (m, 5 H); 6.89-6.81 (m, 2 H); 6.50 (dd, J = 9.85, 1.91 Hz, 1 H); 6.06-6.01 (m, 1 H); 5.20 (d, J = 10.80 Hz, 2 H); 5.16-5.10 (m, 1 H); 5.05 (s, 1 H); 4.14-4.06 (m, 1 H); 3.98-3.90 (m, 2 H); 3.72 (d, J = 14.98 Hz, 3 H); 3.61 (d, J = 12.36 Hz, 2 H); 2.81-2.75 (m, 2 H); 2.70-2.60 (m, 2 H); 2.44-2.29 (m, 1 H); 2.21-1.91 (m, 4 H); 1.73-1.64 (m, 2 H); 1.55-1.28 (m, 6 H). diformate 25C A (DMSO-d6): δ 8.59 (d, J = 9.31 Hz, 1 H); 8.38 (s, 2 H); 8.18 (dd, J = 9.94, 2.25 Hz, 1 H); 7.98 (dd, J = 7.77, 3.44 Hz, 2 H); 7.78-7.71 (m, 1 H); 7.64- 7.57 (m, 2 H); 7.38 (d, J = 8.14 Hz, 1 H); 7.28- 7.17 (m, 3 H); 7.11-7.05 (m, 2 H); 6.95 (d, J = 8.55 Hz, 3 H); 6.83 (d, J = 8.19 Hz, 1 H); 6.50 (dd, J = 9.85, 1.97 Hz, 1 H); 5.88 (d, J = 8.38 Hz, 1 H); 5.19 (s, 2 H); 5.06 (d, J = 17.58 Hz, 2 H); 4.08 (s, 1 H); 3.96-3.89 (m, 2 H); 3.81-3.51 (d, J = 15.32 Hz, 4 H); 2.76-2.71 (m, 2 H); 2.58 (d, J = 16.78 Hz, 2 H); 2.38-2.32 (m, 2 H); 2.10-1.94 (m, 4 H); 1.67 (d, J = 7.71 Hz, 2 H); 1.48-1.25 (m, 6 H). diformate 26C C (DMSO-d6): δ 8.54 (d, J = 9.47 Hz, 1 H); 8.40 (s, 2 H); 8.21-8.15 (m, 1 H); 8.02-7.94 (m, 2 H); 7.75 (dd, J = 13.60, 6.80 Hz, 1 H); 7.61 (dd, J = 14.38, 7.19 Hz, 2 H); 7.51-7.47 (m, 1 H); 7.36-7.29 (m, 1 H); 7.27-7.19 (m, 1 H); 7.09-7.02 (m, 2 H); 6.98-6.89 (m, 3 H); 6.82 (d, J = 8.31 Hz, 1 H); 6.50 (dd, J = 9.84, 2.05 Hz, 1 H); 5.89 (d, J = 8.63 Hz, 1 H); 5.20 (s, 2 H); 5.10 (s, 1 H); 5.03 (s, 1 H); 4.14-4.04 (m, 1 H); 3.96-3.89 (m, 2 H); 3.88- 3.46 (m, 4 H); 2.77-2.72 (m, 2 H); 2.69-2.52 (m, 2 H); 2.34 (t, J = 3.91 Hz, 1 H); 2.17 (s, 1 H); 2.08-1.93 (m, 4 H); 1.68 (d, J = 8.24 Hz, 2 H); 1.51-1.26 (m, 6 H). diformate (continued) 195 27C A (DMSO-d6): δ 8.60-8.54 (m, 1 H); 8.50 (s, 1 H); 8.42 (s, 2 H); 8.17 (d, J = 9.87 Hz, 1 H); 8.01-7.92 (m, 2 H); 7.86-7.82 (m, 2 H); 7.75 (d, J = 7.15 Hz, 1 H); 7.65-7.56 (m, 2 H); 7.49 (d, J = 7.88 Hz, 2 H); 7.37- 7.31 (m, 4 H); 7.29-7.23 (m, 2 H); 7.08-7.01 (m, 2 H); 6.99-6.89 (m, 3 H); 6.49 (dd, J = 9.83, 1.19 Hz, 1 H); .85 (d, J = 8.77 Hz, 1 H); 5.17 (d, J = 21.19 Hz, 4 H); 5.04 (d, J = 8.06 Hz, 2 H); 4.08 (s, 1 H); 3.79-3.55 (m, 4 H); 3.26 (s, 2 H); 2.73 (d, J = 7.03 Hz, 1 H); 2.69-2.52 (m, 3 H); 2.35 (d, J = 6.54 Hz, 1 H); 2.21- 1.89 (m, 5 H); 1.51 (d, J = 22.95 Hz, 4 H). diformate 28C B (CD3OD): δ 8.56 (s, 2 H); 8.38 (dd, J = 9.9, 3.5 Hz, 1 H); 8.03-7.98 (m, 2 H); 7.77-7.69 (m, 1 H); 7.62-7.54 (m, 2 H); 7.36-7.21 (m, 7 H); 7.04 (d, J = 8.2 Hz, 1 H); 6.95-6.79 (m, 3 H); 6.69 (dd, J = 9.8, 3.3 Hz, 1 H); 5.90 (s, 1 H); 5.43-5.36 (m, 1 H); 5.14 (s, 1 H); 4.25-4.14 (m, 1 H); 4.00-3.97 (m, 2 H); 3.85-3.70 (m, H); 3.34 (m, 2 H); 3.22-3.19 (m, 2 H); 3.10-3.05 (m, 2 H); 2.50 (s, 1 H); 2.45-2.33 (m, 1 H); 2.27-2.02 (m, 3 H); 1.82 (s, 4 H); 1.59 (s, 6 H). diformate 29C A (CD3OD): δ 8.56 (s, 2 H); 8.39 (d, J = 9.9 Hz, 1 H); 7.35-7.20 (m, 12 H); 7.04 (d, J = 8.2 Hz, 1 H); 6.90- 6.77 (m, 3 H); 6.70 (d, J = 9.8 Hz, 1 H); 5.88 (s, 1 H); .39 (t, J = 6.7 Hz, 1 H); 5.04 (s, 1 H); 3.94 (t, J = 6.3 Hz, 2 H); 3.89-3.77 (m, 1 H); 3.55-3.18 (m, 6 H); 3.08-2.97 (m, 4 H); 2.69 (t, J = 7.1 Hz, 2 H); 2.41 (s, 1 H); 2.35-2.24 (m, 1H); 2.16-1.87 (m, 4 H); 1.81- 1.68 n(m, 4 H); 1.56-1.39 (m, 6 H) diformate 30C C (CD3OD): δ 8.56 (s, 2 H); 8.38 (dd, J = 9.9, 3.5 Hz, 1 H); 8.03-7.98 (m, 2 H); 7.77-7.69 (m, 1 H); 7.62-7.54 (m, 2 H); 7.36-7.21 (m, 7 H); 7.04 (d, J = 8.2 Hz, 1 H); 6.95-6.79 (m, 3 H); 6.69 (dd, J = 9.8, 3.3 Hz, 1 H); 5.90 (s, 1 H); 5.43-5.36 (m, 1 H); 5.14 (s, 1 H); 4.25-4.14 (m, 1 H); 4.00-3.97 (m, 2 H); 3.85-3.70 (m, H); 3.34 (m, 2 H); 3.22-3.19 (m, 2 H); 3.10-3.05 (m, 2 H); 2.50 (s, 1 H); 2.45-2.33 (m, 1 H); 2.27-2.02 (m, 3 H); 1.82 (s, 4 H); 1.59 (s, 2 H). diformate 31C B (DMSO-d6): δ 8.32-8.21 (m, 3 H); 8.18 (d, J = 9.9 Hz, 1 H); 7.39-7.19 (m, 10 H); 7.09 (d, J = 8.2 Hz, 1 H); 7.01 (s, 1 H); 6.97-6.89 (m, 2 H); 6.88-6.82 (m, 1 H); 6.52 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.0 Hz, 1 H); .13 (t, J = 6.3 Hz, 1 H); 5.00 (s, 2 H); 4.62-4.55 (m, 1 H); 3.97 (t, J = 6.2 Hz, 2 H); 3.16-3.07 (m, 1 H); 2.81-2.52 (m, 9 H); 1.95-1.27 (m, 17 H). diformate (continued) 196 32C B (DMSO-d6): δ 8.32-8.22 (m, 3 H); 8.18 (d, J = 9.9 Hz, 1 H); 7.42-7.18 (m, 10 H); 7.10 (d, J = 8.2 Hz, 1 H); 7.03-6.89 (m, 3 H); 6.88-6.82 (m, 1 H); 6.53 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.1 Hz, 1 H); 5.18 (dd, J = 8.0, 4.5 Hz, 1 H); 5.00 (s, 2 H); 4.64-4.57 (m, 1 H); 4.02 (t, J = 6.2 Hz, 2 H); 3.20-3.09 (m, 1 H); 2.88-2.52 (m, 7 H); 2.40-2.30 (m, 2 H); 1.97-1.76 (m, 2 H); 1.73-1.16 (m, 17 H) diformate 33C B (DMSO-d6): δ 8.33-8.23 (m, 3 H); 8.17 (d, J = 9.9 Hz, 1 H); 7.42-7.19 (m, 10 H); 7.10 (d, J = 8.2 Hz, 1 H); 7.01 (s, 1 H); 6.99-6.89 (m, 2 H); 6.88-6.83 (m, 1 H); 6.53 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.2 Hz, 1 H); 5.19 (dd, J = 8.2, 4.5 Hz, 1 H); 5.01 (s, 2 H); 4.64-4.56 (m, 1 H); 4.03 (t, J = 6.1 Hz, 2 H); 3.20- 3.09 (m, 1 H); 2.89-2.52 (m, 9 H); 1.97-1.76 (m, 2 H); 1.67-1.28 (m, 13 H). diformate 34C A (DMSO-d6): δ 8.39 (d, J = 9.32 Hz, 1 H); 8.30 (s, 2 H); 8.18 (d, J = 9.94 Hz, 1 H); 7.93 (s, 1 H); 7.83 (d, J = 7.72 Hz, 1 H); 7.65-7.53 (m, 1 H); 7.51-7.44 (m, 1 H); 7.35-7.30 (m, 4 H); 7.26 (d, J = 5.91 Hz, 1 H); 7.11 (d, J = 8.18 Hz, 1 H); 6.96 (d, J = 8.13 Hz, 1 H); 6.53 (d, J = 9.86 Hz, 1 H); 5.94 (d, J = 8.55 Hz, 1 H); 5.21 (dd, J = 8.61, 4.05 Hz, 1 H); 4.60 (s, 1 H); 4.28-4.21 (m, 2 H); 3.12 (s, 1 H); 2.96-2.85 (m, 2 H); 2.80-2.57 (m, 7 H); 1.92 (s, 1 H); 1.81 (s, 1 H); 1.86-1.39 (m, 5 H); 1.32 (d, J = 29.30 Hz, 10 H). diformate 35C A (DMSO-d6): δ 8.39 (d, J = 9.08 Hz, 1 H); 8.32 (s, 2 H); 8.18 (d, J = 9.91 Hz, 1 H); 7.93 (s, 1 H); 7.83 (d, J = 7.65 Hz, 1 H); 7.58 (s, 1 H); 7.52-7.44 (m, 1 H); 7.34 (d, J = 4.53 Hz, 4 H); 7.26 (d, J = 6.13 Hz, 1 H); 7.11 (d, J = 8.14 Hz, 1 H); 6.99-6.91 (m, 1 H); 6.56-6.47 (m, 1 H); 5.94 (d, J = 7.51 Hz, 1 H); 5.24- .18 (m, 1 H); 4.59 (s, 1 H); 4.29-4.21 (m, 2 H); 3.12 (d, J = 12.48 Hz, 1 H); 2.88 (d, J = 9.45 Hz, 2 H); 2.69 (d, J = 52.79 Hz, 6 H); 1.92 (s, 1 H); 1.81 (s, 1 H); 1.72-1.08 (m, 18 H). diformate 36C A (DMSO-d6): δ 8.38 (d, J = 9.05 Hz, 1 H); 8.30 (d, J = 4.26 Hz, 2 H); 8.18 (d, J = 9.90 Hz, 1 H); 7.93 (s, 1 H); 7.83 (d, J = 7.68 Hz, 1 H); 7.58 (s, 1 H); 7.48 (t, J = 7.67 Hz, 1 H); 7.34 (d, J = 4.51 Hz, 4 H); 7.26 (d, J = 5.85 Hz, 1 H); 7.10 (d, J = 8.16 Hz, 1 H); 6.95 (d, J = 8.11 Hz, 1 H); 6.52 (d, J = 9.85 Hz, 1 H); 5.94 (d, J = 8.11 Hz, 1 H); 5.17 (s, 1 H); 4.58 (s, 1 H); 4.25 (t, J = 6.47 Hz, 2 H); 3.10 (s, 1 H); 2.91- 2.52 (m, 8 H); 1.97-1.72 (m, 2 H); 1.73-1.65 (m, 2 H); 1.74-1.20 (m, 12 H). diformate (continued) 197 37C A (DMSO d6): δ 8.30 (s, 1 H); 8.27-8.20 (m, 1 H); 8.17-8.11 (m, 3 H); 7.65 (d, J = 7.9 Hz, 2 H); 7.41 (d, J = 8.0 Hz, 2 H); 7.36-7.15 (m, 8 H); 7.12-7.04 (m, 2 H); 6.98-6.87 (m, 3 H); 6.49 (d, J = 9.8 Hz, 1 H); 5.83 (d, J = 9.2 Hz, 1 H); 5.23 (s, 2 H); 5.08 (dd, J = 7.8, 4.3 Hz, 1 H); 4.57 (s, 1 H); 3.79 (s, 2 H); 3.10 (s, 2 H); 2.76-2.63 (m, 6 H); 1.90 (s, 1 H); 1.80 (s, 1 H); 1.58 (s, 1 H); 1.47 (s, 1 H); 1.33 (s, 1 H). diformate 38C A (DMSO-d6): δ 8.39 (d, J = 8.88 Hz, 1 H); 8.29 (s, 2 H); 8.18 (d, J = 9.91 Hz, 1 H); 7.93 (s, 1 H); 7.84 (d, J = 7.67 Hz, 1 H); 7.59 (d, J = 7.47 Hz, 1 H); 7.52- 7.44 (m, 1 H); 7.34 (d, J = 4.53 Hz, 4 H); 7.26 (d, J = 5.97 Hz, 1 H); 7.10 (d, J = 8.16 Hz, 1 H); 6.95 (d, J = 8.13 Hz, 1 H); 6.52 (d, J = 9.86 Hz, 1 H); 5.94 (d, J = 8.37 Hz, 1 H); 5.19-5.12 (m, 1 H); 4.58 (s, 1 H); 4.30-4.22 (m, 2 H); 3.10 (s, 1 H); 2.84 (d, J = 6.23 Hz, 2 H); 2.79-2.58 (m, 6 H); 1.91 (s, 1 H); 1.80 (s, 1 H); 1.76-1.64 (m, 2 H); 1.62-1.32 (m, 8 H). diformate 39C B (DMSO-d6): δ 8.53 (s, 1 H); 8.39 (d, J = 9.67 Hz, 1 H); 8.28 (s, 2 H); 8.18 (d, J = 9.93 Hz, 1 H); 7.99 (s, 1 H); 7.87 (dd, J = 14.46, 7.77 Hz, 3 H); 7.65-7.58 (m, 1 H); 7.55-7.47 (m, 3 H); 7.34 (d, J = 4.80 Hz, 4 H); 7.28-7.23 (m, 1 H); 7.11 (d, J = 8.18 Hz, 1 H); 6.96 (d, J = 8.12 Hz, 1 H); 6.53 (d, J = 9.86 Hz, 1 H); 5.96 (d, J = 7.79 Hz, 1 H); 5.40 (s, 2 H); 5.21 (dd, J = 8.54, 4.15 Hz, 1 H); 4.59 (s, 1 H); 3.33-3.21 (m, 2 H); 3.12 (s, 1 H); 2.90-2.52 (m, 8 H); 1.85 (d, J = 49.16 Hz, 2 H); 1.71-1.21 (m, 8 H). diformate 40C B (CD3OD): δ 8.52 (s, 2 H); 8.38 (d, J = 9.94 Hz, 1 H); 8.00 (d, J = 11.22 Hz, 2 H); 7.88 (d, J = 7.98 Hz, 2 H); 7.64 (d, J = 7.97 Hz, 2 H); 7.59-7.45 (m, 2 H); 7.33 (dd, J = 24.56, 7.68 Hz, 6 H); 7.04 (d, J = 8.21 Hz, 1 H); 6.70 (d, J = 9.84 Hz, 1 H); 6.00 (s, 1 H); .45 (s, 2 H); 5.42-5.35 (m, 1 H); 4.60 (s, 1 H); 3.53 (m, 1 H); 3.23-3.16 (m, 9 H); 2.97-2.89 (m, 2 H); 2.23-1.48 (m, 9 H). diformate 41C B (DMSO-d6): δ 8.40 (d, J = 8.99 Hz, 1 H); 8.27 (s, 2 H); 8.18 (d, J = 9.90 Hz, 1 H); 7.97 (s, 1 H); 7.86 (d, J = 7.68 Hz, 1 H); 7.67-7.52 (m, 1 H); 7.53-7.44 (m, 1 H); 7.38-7.31 (m, 6 H); 7.29-7.21 (m, 3 H); 7.15- 7.05 (m, 1 H); 6.94 (d, J = 8.13 Hz, 1 H); 6.52 (d, J = 9.86 Hz, 1 H); 5.95 (d, J = 8.61 Hz, 1 H); 5.31 (s, 2 H); 5.17-5.10 (m, 1 H); 4.60 (s, 1 H); 3.14 (s, 1 H); 3.00-2.54 (m, 11 H); 1.93 (s, 1 H); 1.80 (s, 1 H); 1.60 (s, 1 H); 1.50 (s, 1 H); 1.36 (s, 1 H). diformate (continued) 198 42C C (DMSO-d6): δ 9.20-9.06 (m, 1 H); 8.32 (s, 2 H); 8.18 (d, J = 9.91 Hz, 1 H); 7.93 (d, J = 8.61 Hz, 3 H); 7.78 (d, J = 7.53 Hz, 1 H); 7.52-7.39 (m, 4 H); 7.34 (d, J = 5.28 Hz, 4 H); 7.25 (s, 1 H); 7.09 (d, J = 8.18 Hz, 1 H); 6.95 (d, J = 8.13 Hz, 1 H); 6.51 (d, J = 9.84 Hz, 1 H); 5.91 (d, J = 8.42 Hz, 1 H); 5.19-5.12 (m, 1 H); 4.61-4.50 (m, 3 H); 4.30- 4.24 (m, 2 H); 3.21-3.02 (m, 1 H); 2.88-2.49 (m, 8 H); 1.91 (s, 1 H); 1.92-1.27 (m, 9 H). diformate 43C A (CD3OD): δ 8.54 (s, 2 H); 8.35 (d, J = 9.8 Hz, 1 H); 7.72 (d, J = 8.1 Hz, 2 H); 7.44 (d, J = 8.0 Hz, 2 H); 7.32-7.21 (m, 11 H); 7.03 (d, J = 8.2 Hz, 1 H); 6.91 (m, 4 H); 6.66 (dd, J = 9.8, 1.1 Hz, 1 H); .88 (s, 1 H); 5.39-5.34 (m, 1 H); 5.11 (s, 2 H); 4.78-4.73 (m, 1 H); 4.32-4.26 (m, 1 H); 4.14-4.09 (m, 1 H); 3.56 (s, 1 H); 3.30-3.03 (m, 11 H); 1.89- 1.64 (m, 10 H). diformate 44C B (DMSO-d6): δ 8.36 (s, 2 H); 8.27 (d, J = 9.3 Hz, 1 H); 8.18 (d, J = 9.9 Hz, 1 H); 7.98-7.89 (m, 2 H); 7.47-7.38 (m, 2 H); 7.35-7.22 (m, 5 H); 7.21-7.16 (m, 1 H); 7.13-6.91 (m, 5 H); 6.50 (d, J = 9.9 Hz, 1 H); 5.84 (d, J = 9.4 Hz, 1 H); 5.56 (s, 2 H); .13-5.07 (m, 1 H); 4.59 (d, J = 7.5 Hz, 1 H); 3.11 (d, J = 10.6 Hz, 1 H); 2.96-2.78 (m, 6 H); 2.73- 2.44 (m, 5 H); 1.91 (s, 1 H); 1.79 (s, 1 H); 1.59 (s, 1 H); 1.48 (s, 1 H); 1.34 (s, 1 H). diformate 45C B (DMSO-d6): δ 8.49-8.14 (m, 3 H); 8.20-8.13 (m, 3 H); 7.38-7.30 (m, 5 H); 7.29-7.22 (m, 1 H); 7.11 (d, J = 8.2 Hz, 1 H); 6.96 (d, J = 8.1 Hz, 1 H); 6.57-6.49 (m, 1 H); 5.92 (d, J = 9.1 Hz, 1 H); 5.21 (dd, J = 8.5, 4.2 Hz, 1 H); 4.60 (s, 1 H); 4.04-3.96 (m, 2 H); 3.18-3.07 (m, 1 H); 2.91-2.48 (m, 8 H); 1.92 (s, 1 H); 1.75-1.64 (m, 2 H); 1.52 (s, 4 H); 1.38 (d, J = 10.7 Hz, 4 H); 1.27 (s, 9 H). diformate 46C A (DMSO-d6): δ 8.53-8.16 (m, 4H); 7.42-7.36 (m, 2 H); 7.24-7.22 (m, 2 H); 7.11-7.04 (m, 2 H); 6.91- 6.89 (m, 2 H); 6.50 (d, J = 9.6 Hz, 1 H); 5.95 (s, 1 H); 5.02-4.99 (dd, J = 7.9, 4.5 Hz, 1 H); 4.60-4.53 (m, 1 H); 3.92 (t, J = 6.5 Hz, 2 H); 3.12-3.02 (m, 1 H); 2.77-2.53 (m, 6H); 1.92-1.20 (m, 21 H). diformate (continued) 199 47C A (DMSO-d6): δ 8.26 (s, 2 H); 8.20 (d, J = 9.51 Hz, 1 H); 8.13 (d, J = 9.93 Hz, 1 H); 7.76 (d, J = 7.99 Hz, 1 H); 7.57 (s, 1 H); 7.43 (d, J = 8.10 Hz, 1 H); 7.27-7.13 (m, 6 H); 7.04 (d, J = 8.17 Hz, 1 H); 6.98 (s, 1 H); 6.90 (d, J = 8.08 Hz, 2 H); 6.83 (dd, J = 8.27, 2.48 Hz, 1 H); 6.45 (d, J = 9.86 Hz, 1 H); 5.76 (d, J = 9.32 Hz, 1 H); 5.21-5.02 (m, 3 H); 4.53 (m, 1 H); 4.24 (t, J = 6.14 Hz, 2 H); 3.12-3.02 (m, 1 H); 2.88-2.49 (m, 9 H); 1.85 (m, 1 H); 1.80-1.20 (m, 8 H). diformate 48C C (DMSO-d6): δ 8.32 (s, 2 H); 8.23 (d, J = 9.88 Hz, 1 H); 8.18 (d, J = 9.92 Hz, 1 H); 7.89 (t, J = 7.85 Hz, 1 H); 7.39-7.17 (m, 8 H); 7.13-6.98 (m, 2 H); 6.97-6.85 (m, 3 H); 6.50 (d, J = 9.85 Hz, 1 H); .82 (d, J = 9.01 Hz, 1 H); 5.18 (s, 2 H); 5.11 (t, J = 6.33 Hz, 1 H); 4.57 (s, 1 H); 4.29 (t, J = 6.33 Hz, 2 H); 3.09 (s, 1 H); 2.78 (d, J = 6.45 Hz, 2 H); 2.72 (s, 6 H); 1.90 (s, 1 H); 1.80-1.68 (m, 3 H); 1.73-1.40 (m, 6 H). diformate 49C C (DMSO-d6); δ 9.09-9.05 (m, 1 H); 8.36-8.23 (m, 4 H); 8.18 (d, J = 9.94 Hz, 1 H); 7.63 (d, J = 8.19 Hz, 1 H); 7.32-7.18 (m, 6 H); 7.18-6.98 (m, 2 H); 6.98-6.88 (m, 3 H); 6.55-6.47 (m, 1 H); 5.82 (d, J = 9.28 Hz, 1 H); 5.37-5.19 (m, 2 H); 5.20 (dd, J = 8.41, 4.37 Hz, 1 H); 4.59 (s, 1 H); 4.36-4.30 (m, 2 H); 3.19-3.08 (m, 1 H); 2.92-2.55 (m, 8 H); 2.01- 1.84 (m, 1 H); 1.95-1.39 (m, 9 H). diformate 50C B (DMSO-d6): δ 8.39-8.12 (m, 3 H); 8.18 (d, J = 9.94 Hz, 1 H); 7.33-7.19 (m, 7 H); 7.15-7.07 (m, 1 H); 7.04 (s, 1 H,); 6.99-6.89 (m, 3 H); 6.76 (d, J = 3.48 Hz, 1 H); 6.52 (d, J = 9.86 Hz, 1 H); 5.83 (d, J = 9.2 Hz, 1 H); 5.23-5.11 (m, 3 H); 4.60 (s, 1 H); 4.28-4.21 (m, 2 H); 3.14 (dd, J = 14.7, 8.6 Hz, 1 H); 2.88-2.75 (m, 5 H); 2.72-2.48 (m, 7 H); 1.92 (d, J = 5.8 Hz, 1 H); 1.72 (t, J = 6.7 Hz, 3 H); 1.62 (d, J = 10.3 Hz, 3 H); 1.56-1.29 (m, 3 H).. diformate 51C C (DMSO-d6): δ 8.91-8.83 (m, 1 H); 8.37-8.12 (m, 3 H); 8.17 (d, J = 9.9 Hz, 1 H); 7.32-7.17 (m, 6 H); 7.10 (d, J = 8.1 Hz, 1 H); 7.05-6.87 (m, 4 H); 6.52 (d, J = 9.8 Hz, 1 H); 5.82 (d, J = 9.3 Hz, 1 H); 5.27 (s, 2 H); 5.18 (t, J = 5.9 Hz, 1 H); 4.59 (s, 1 H); 4.26 (t, J = 6.2 Hz, 2 H); 3.18-3.09 (m, 1 H); 2.86 (d, J = 7.2 Hz, 2 H); 2.79 (s, 5 H); 2.68- 2.66 (m, 1 H); 1.92 (s, 1 H); 1.75-1.56 (m, 5 H); 1.50 (s, 2 H); 1.36 (s, 2 H). diformate (continued) 200 52C A (DMSO-d6): δ 8.31-8.22 (m, 3 H); 8.17 (d, J = 9.9 Hz, 1 H); 8.03 (s, 1 H); 7.92 (d, J = 7.8 Hz, 1 H); 7.71 (d, J = 7.7 Hz, 1 H); 7.54 (t, J = 7.7 Hz, 1 H); 7.36-7.18 (m, 6 H); 7.12-7.02 (m, 2 H); 6.98- 6.87 (m, 3 H); 6.52 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.3 Hz, 1 H); 5.21-5.13 (m, 3 H); 4.63-4.56 (m, 1 H); 4.30 (t, J = 6.2 Hz, 2 H); 3.18-3.08 (m, 1 H); 2.91-2.52 (m, 9 H); 1.95-1.89 (m, 1 H); 1.86- 1.30 (m, 8 H). diformate 53C A (DMSO-d6): δ 8.30-8.24 (m, 3 H); 8.18 (d, J = 9.9 Hz, 1 H); 7.31-7.28 (m, 4 H); 7.26-7.20 (m, 2 H); 7.14-7.07 (m, 1 H); 6.96-6.94 (m, 3 H); 6.79-6.76 (m, 1 H); 6.54-6.51 (m, 1 H); 5.82-5.79 (m, 1 H); .19-5.16 (m, 1 H); 4.75 (s, 2 H); 4.60-4.56 (m, 1 H); 4.10-4.06 (m, 2 H); 3.11-3.09 (m, 1 H); 2.86- 2.50 (m, 8 H); 1.92-1.88 (m, 1 H); 1.80-1.75 (m, 1 H); 1.58-1.48 (m, 7 H); 1.34-1.26 (m, 3 H). diformate 54C A (DMSO-d6): δ 8.30-8.24 (m, 3 H); 8.18 (d, J = 9.9 Hz, 1 H); 7.32-7.28 (m, 4 H); 7.24-7.20 (m, 2 H); 7.11-7.09 (m, 1 H); 6.96-6.93 (m, 3 H); 6.78-6.76 (m, 1 H); 6.53-6.51 (m, 1 H); 5.82-5.80 (m, 1 H); .17-5.14 (m, 1 H); 4.75 (s, 2 H); 4.59-4.55 (m, 1 H); 4.09-4.06 (m, 2 H); 3.15-3.08 (m, 1 H); 2.83- 2.50 (m, 8 H); 1.91-1.87 (m, 1 H); 1.81-1.75 (m, 1 H); 1.58-1.47 (m, 7 H); 1.33-1.25 (m, 3 H). diformate 55C C (DMSO-d6): δ 8.32-8.27 (m, 3 H); 8.20 (d, J = 9.9 Hz, 1 H); 7.32-7.26 (m, 4 H); 7.25-7.20 (m, 2 H); 7.13-7.10 (m, 1 H); 6.98-6.94 (m, 3 H); 6.79-6.76 (m, 1 H); 6.55-6.52 (m, 1 H); 5.83-5.80 (m, 1 H); .29-5.26 (m, 1 H); 4.75 (s, 2 H); 4.63-4.59 (m, 1 H); 4.09-4.06 (m, 2 H); 3.20-3.15 (m, 1 H); 2.98- 2.50 (m, 8 H); 1.98-1.87 (m, 1 H); 1.92-1.69 (m, 1 H); 1.76-1.28 (m, 5 H); 1.48-1.26 (m, 2 H); 1.45-1.09 (m, 4 H). diformate 56C A (DMSO-d6): δ 8.35-8.20 (m, 3 H); 8.19 (d, J = 9.9 Hz, 1 H); 7.34-7.27 (m, 4 H); 7.26-7.19 (m, 2 H); 7.14-7.07 (m, 1 H); 7.00-6.90 (m, 3 H); 6.80-6.73 (m, 1 H); 6.56-6.50 (m, 1 H); 5.86-5.78 (m, 1 H); .24-5.19 (m, 1 H); 4.75 (s, 2 H); 4.68-4.52 (m, 1 H); 4.11-4.04 (m, 2 H); 3.23-3.03 (m, 1 H); 2.95- 2.82 (m, 2 H); 2.91-2.61 (m, 4 H); 2.73-2.50 (m, 3 H); 1.98-1.87 (m, 1 H); 1.92-1.69 (m, 1 H); 1.76-1.28 (m, 5 H); 1.48-1.26 (m, 2 H); 1.45-1.09 (m, 4 H). diformate (continued) 201 57C A (DMSO-d6): δ 8.57 (t, J = 5.5 Hz, 1 H); 8.32 (s, 2 H); 8.27-8.15 (m, 2 H); 7.84 (d, J = 8.0 Hz, 2 H); 7.50 (d, J = 8.0 Hz, 2 H); 7.35-7.19 (m, 6 H); 7.11-7.02 (m, 2 H); 6.96-6.86 (m, 3 H); 6.50 (d, J = 9.9 Hz, 1 H); 5.84-5.79 (m, 1 H); 5.16-5.09 (m, 3 H); 4.60-4.54 (m, 1 H); 3.36-3.28 (m, 2 H); 3.15-3.05 (m, 1 H); 2.83-2.52 (m, 9 H); 1.94-1.68 (m, 4 H); 1.65-1.26 (m, 3 H). diformate 58C A (DMSO-d6): δ 8.45 (t, J = 5.6 Hz, 1 H); 8.32 (s, 1 H); 8.27-8.16 (m, 2 H); 7.83 (d, J = 8.1 Hz, 2 H); 7.50 (d, J = 8.0 Hz, 2 H); 7.36-7.19 (m, 6 H); 7.12-7.03 (m, 2 H); 6.96-6.86 (m, 3 H); 6.48 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.2 Hz, 1 H); 5.14 (s, 2 H); 5.04 (t, J = 6.2 Hz, 1 H); 4.61-4.53 (m, 1 H); 3.40-3.32 (m, 2 H); 3.14-3.04 (m, 1 H); 2.83- 2.52 (m, 9 H); 1.93-1.73 (m, 2 H); 1.65-1.26 (m, 3 H). formate 59C A (DMSO-d6 85°C): δ 8.22-8.11 (m, 2 H); 7.76-7.65 (m, 1 H); 7.48-7.38 (m, 2 H); 7.36-7.15 (m, 8 H); 7.10-6.82 (m, 5 H); 6.51-6.40 (m, 1 H); 5.85-5.75 (m, 1 H); 5.13-4.94 (m, 3 H); 4.64-4.52 (m, 1 H); 3.40-3.22 (m, 4 H); 3.14-3.00 (m, 1 H); 2.82-2.43 (m, 9 H); 1.94-1.83 (m, 1 H); 1.81-1.55 (m, 4 H); 1.53-1.40 (m, 1 H); 1.36-1.23 (m, 1 H); 1.12-1.00 (m, 3 H). formate 60C B (DMSO-d6 85°C): δ 8.22-8.15 (m, 3 H); 7.73 (s, 1 H); 7.46 (d, J = 7.85 Hz, 2 H); 7.37-7.27 (m, 6 H); 7.26-7.19 (m, 2 H); 7.08 (d, J = 8.12 Hz, 2 H); 7.03 (s, 1 H); 6.95 (d, J = 7.74 Hz, 2 H); 6.48 (d, J = 9.88 Hz, 1 H); 5.83 (d, J = 7.98 Hz, 1 H); .11 (s, 2 H); 5.05-4.99 (m, 1 H); 4.63-4.58 (m, 1 H); 3.39 (s, 2 H); 3.09 (dd, J = 14.46, 8.25 Hz, 1 H); 2.91 (s, 3 H); 2.81-2.49 (m, 9 H); 1.93-1.89 (m, 1 H); 1.73-1.55 (m, 4 H); 1.52-1.45 (m, 1 H); 1.31 (d, J = 11.44 Hz, 1 H). diformate 61C C (DMSO-d6 85°C): δ 8.25-8.15 (m, 3 H); 7.73 (s, 1 H); 7.46 (d, J = 7.85 Hz, 2 H); 7.33-7.20 (m, 7 H); 7.09 (d, J = 8.12 Hz, 1 H); 7.03 (m, 1 H); 6.97-6.87 (m, 3 H); 6.50 (d, J = 3.46 Hz, 1 H); .83 (d, J = 8.55 Hz, 1 H); 5.11 (s, 2 H); 5.07- .03 (m, 1 H); 4.63-4.58 (m, 1 H); 4.00 (s, 1 H); 3.27 (t, J = 7.50 Hz, 2 H); 3.09 (dd, J = 14.43, 8.27 Hz, 1 H); 2.80-2.5 (m, 9 H); 1.93-1.89 (m, 1 H); 1.78-1.68 (m, 3 H); 1.66-1.56 (m, 1 H); 1.53- 1.44 (m, 1 H); 1.32 (q, J = 9.86 Hz, 1 H); 1.15 (d, J = 6.72 Hz, 6 H). diformate (continued) 202 62C A (DMSO-d6): δ 8.46 (t, J = 5.7 Hz, 1 H); 8.29 (s, 2 H); 8.24 (d, J = 9.3 Hz, 1 H); 8.18 (d, J = 9.9 Hz, 1 H); 7.84 (d, J = 7.9 Hz, 2 H); 7.50 (d, J = 7.9 Hz, 2 H); 7.36-7.27 (m, 4 H); 7.27-7.18 (m, 2 H); 7.09 (d, J = 8.1 Hz, 1 H); 7.04 (s, 1 H); 6.98-6.85 (m, 3 H); 6.52 (d, J = 9.9 Hz, 1 H); 5.81 (d, J = 8.9 Hz, 1 H); 5.18- .10 (m, 3 H); 4.62-4.54 (m, 1 H); 4.00 (t, J = 6.0 Hz, 2 H); 3.17-3.06 (m, 3 H); 2.86-2.53 (m, 9 H); 2.29- 2.19 (m, 1 H); 1.96-1.86 (m, 3 H); 1.85-1.72 (m, 3 H); 1.66-1.20 (m, 10 H); 1.05-0.90 (m, 2 H). diformate 63C A (DMSO-d6): 10.80-10.00 (br s, 1 H); 8.70 (t, J = 6.32 Hz, 1 H); 8.27 (s, 2 H); 8.19 (d, J = 9.92 Hz, 1 H); 7.84 (t, J = 6.84 Hz, 2 H), 7.51 (d, J = 7.83 Hz, 2 H); 7.31 (s, 4 H); 7.23 (t, J = 7.47 Hz, 2 H); 7.11-7.02 (m, 2 H); 6.96-6.85 (m, 3 H); 6.50 (dd, J = 9.80, 3.32 Hz, 1 H); 5.81 (s, 1 H); 5.14 (s, 2 H); 5.07 (d, J = 10.80 Hz, 1 H); 4.90 (t, J = 6.69 Hz, 1 H); 4.60 (s, 1 H); 3.63 (d, J = 2.45 Hz, 3 H); 3.50-3.32 (m, 3 H); 3.15 (s, 1 H); 2.98 (s, 3 H); 2.90 (d, J = 6.19 Hz, 1 H), 2.77 (m, 7 H); 2.68 (s, 3 H); 1.94 (s, 1 H); 1.81 (s, 1 H); 1.61 (s, 1 H); 1.51 (s, 1 H); 1.37 (s, 1 H). diformate 64C C (DMSO-d6): δ 8.30-8.21 (m, 3 H); 8.19 (d, J = 9.9 Hz, 1 H); 7.97 (d, J = 7.9 Hz, 2 H); 7.57 (d, J = 7.9 Hz, 2 H); 7.30 (s, 4 H); 7.28-7.19 (m, 2 H); 7.10 (d, J = 8.1 Hz, 1 H); 7.03 (s, 1 H); 6.92 (dd, J = 24.4, 8.0 Hz, 3 H); 6.53 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.1 Hz, 1 H); .20-5.11 (m, 3 H); 4.59 (s, 1 H); 4.12 (d, J = 6.2 Hz, 2 H); 3.13 (m, 1 H); 2.88-2.55 (m, 8 H); 1.96-1.32 (m, 12 H); 1.14-0.88 (m, 4 H) diformate 65C B (DMSO-d6): δ 8.30 (s, 1 H); 8.27-8.20 (m, 1 H); 8.17- 8.11 (m, 3 H); 7.65 (d, J = 7.9 Hz, 2 H); 7.41 (d, J = 8.0 Hz, 2 H); 7.36-7.15 (m, 8 H); 7.12-7.04 (m, 2 H); 6.98-6.87 (m, 3 H); 6.49 (d, J = 9.8 Hz, 1 H); 5.83 (d, J = 9.2 Hz, 1 H); 5.23 (s, 2 H); 5.08 (dd, J = 7.8, 4.3 Hz, 1 H); 4.57 (s, 1 H); 3.79 (s, 2 H); 3.10 (s, 2 H); 2.76-2.63 (m, 6 H); 1.90 (s, 1 H); 1.80 (s, 1 H); 1.58 (s, 1 H); 1.47 (s, 1 H); 1.33 (s, 1 H). diformate 66C C (DMSO-d6): δ 8.32-8.20 (m, 2 H); 8.17 (d, J = 10.0 Hz, 2 H); 8.02 (d, J = 7.9 Hz, 2 H); 7.58 (d, J = 7.9 Hz, 2 H); 7.31 (s, 4 H); 7.24 (t, J = 7.8 Hz, 2 H); 7.12- 7.01 (m, 2 H); 6.98-6.85 (m, 3 H); 6.51 (d, J = 9.8 Hz, 1 H); 5.82 (d, J = 8.9 Hz, 1 H); 5.19 (s, 2 H); 5.11 (t, J = 6.2 Hz, 1 H); 4.70 (s, 2 H); 4.58 (s, 1 H); 3.16-3.09 (m, 4 H); 2.79 (d, J = 6.5 Hz, 2 H); 2.74-2.65 (m, 4 H); 1.91 (s, 1 H); 1.80 (s, 1 H); 1.64 (t, J = 11.6 Hz, 5 H); 1.48 (s, 1 H); 1.34 (s, 1 H). diformate (continued) 203 67C A (DMSO-d6): δ 8.30-8.16 (m, 3 H); 8.19 (d, J = 10.0 Hz, 1 H); 8.00 (d, J = 8.0 Hz, 2 H); 7.59 (d, J = 8.0 Hz, 2 H); 7.31 (s, 4 H); 7.28-7.19 (m, 2 H); 7.09 (d, J = 8.1 Hz, 1 H); 7.04 (s, 1 H); 6.97-6.86 (m, 3 H); 6.53 (d, J = 10.0 Hz, 1 H); 5.81 (m, 1 H); 5.19 (s, 2 H); .11 (t, J = 5.2 Hz, 1 H); 4.93 (s, 2 H); 4.58 (s, 1 H); 4.14 (t, J = 6.3 Hz, 2 H); 3.16-3.04 (m, 1 H); 2.86- 2.62 (m, 8 H); 1.90 (s, 1 H); 1.79 (s, 1 H); 1.69-1.41 (m, 7 H); 1.34 (s, 1 H). diformate 68C A (DMSO-d6): δ 8.30-8.16 (m, 3 H); 8.00 (d, J = 8.1 Hz, 2 H); 7.60 (d, J = 8.0 Hz, 2 H); 7.31-7.18 (m, 6 H); 7.12 (d, J = 8.2 Hz, 1 H); 7.03 (s, 1 H); 6.96 (t, J = 6.8 Hz, 2 H); 6.89 (dd, J = 8.2, 2.5 Hz, 1 H); 6.55 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.2 Hz, 1 H); 5.25 (dd, J = 8.9, 3.9 Hz, 1 H); 5.19 (s, 2 H); 4.94 (s, 2 H); 4.60 (s, 1 H); 4.14 (t, J = 6.4 Hz, 2 H); 3.16 (m, 1 H); 2.98- 2.89 (m, 2 H); 2.85-2.59 (m, 7 H); 1.94 (s, 1 H); 1.81 (s, 1 H); 1.65-1.55 (m, 6 H); 1.40-1.30 (m, 4 H). formate 69C C (DMSO-d6): δ 8.32-8.20 (m, 3 H); 8.17 (d, J = 9.9 Hz, 1 H); 7.96 (d, J = 8.1 Hz, 2 H); 7.56 (d, J = 8.0 Hz, 2 H); 7.32-7.18 (m, 6 H); 7.08-7.01 (m, 2 H); 6.97-6.84 (m, 3 H); 6.49 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.3 Hz, 1 H); 5.17 (s, 2 H); 5.09-5.02 (m, 1 H); 4.58 (s, 1 H); 4.42-4.37 (m, 2 H); 3.76-3.71 (m, 2 H); 3.61-3.55 (m, 2 H); 3.11 (t, J = 10.6 Hz, 1 H); 2.82-2.50 (m, 9 H); 1.91 (s, 1 H); 1.80 (s, 1 H); 1.59 (s, 1 H); 1.48 (s, 1 H); 1.35 (s, 1 H) diformate 70C C (DMSO-d6): δ 8.31-8.19 (m, 2 H); 8.16 (d, J = 9.9 Hz, 1 H); 7.96 (d, J = 8.1 Hz, 2 H); 7.56 (d, J = 8.0 Hz, 2 H); 7.31-7.18 (m, 6 H); 7.08 (d, J = 8.2 Hz, 1 H); 7.03 (s, 1 H); 6.97-6.90 (m, 2 H); 6.88 (dd, J = 8.3, 2.5 Hz, 1 H); 6.52 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.1 Hz, 1 H); 5.18-5.09 (m, 3 H); 4.57 (s, 1 H); 4.42-4.37 (m, 2 H); 3.72-3.67 (m, 2 H); 3.46 (s, 2 H); 3.21-3.02 (m, 1 H); 2.81-2.50 (m, 10 H); 1.90 (s, 1 H); 1.79 (s, 1 H); 1.53 (s, 5 H); 1.34 (s, 1 H). formate 71C A (DMSO-d6): δ 8.30-8.16 (m, 3 H); 8.00 (d, J = 8.1 Hz, 2 H); 7.60 (d, J = 8.0 Hz, 2 H); 7.31-7.18 (m, 6 H); 7.12 (d, J = 8.2 Hz, 1 H); 7.03 (s, 1 H); 6.96 (t, J = 6.8 Hz, 2 H); 6.89 (dd, J = 8.2, 2.5 Hz, 1 H); 6.55 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.2 Hz, 1 H); 5.25 (dd, J = 8.9, 3.9 Hz, 1 H); 5.19 (s, 2 H); 4.94 (s, 2 H); 4.60 (s, 1 H); 4.14 (t, J = 6.4 Hz, 2 H); 3.16 (m, 1 H); 2.98- 2.89 (m, 2 H); 2.85-2.59 (m, 7 H); 1.94 (s, 1 H); 1.81 (s, 1 H); 1.65-1.55 (m, 6 H); 1.40-1.30 (m, 4 H). formate (continued) 204 72C C (DMSO-d6): δ 8.32-8.20 (m, 3 H); 8.17 (d, J = 9.9 Hz, 1 H); 7.96 (d, J = 8.1 Hz, 2 H); 7.56 (d, J = 8.0 Hz, 2 H); 7.32-7.18 (m, 6 H); 7.08-7.01 (m, 2 H); 6.97-6.84 (m, 3 H); 6.49 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.3 Hz, 1 H); 5.17 (s, 2 H); 5.09-5.02 (m, 1 H); 4.58 (s, 1 H); 4.42-4.37 (m, 2 H); 3.76-3.71 (m, 2 H); 3.61-3.55 (m, 2 H); 3.11 (t, J = 10.6 Hz, 1 H); 2.82-2.50 (m, 9 H); 1.91 (s, 1 H); 1.80 (s, 1 H); 1.59 (s, 1 H); 1.48 (s, 1 H); 1.35 (s, 1 H) diformate 73C C (DMSO-d6): δ 8.31-8.19 (m, 2 H); 8.16 (d, J = 9.9 Hz, 1 H); 7.96 (d, J = 8.1 Hz, 2 H); 7.56 (d, J = 8.0 Hz, 2 H); 7.31-7.18 (m, 6 H); 7.08 (d, J = 8.2 Hz, 1 H); 7.03 (s, 1 H); 6.97-6.90 (m, 2 H); 6.88 (dd, J = 8.3, 2.5 Hz, 1 H); 6.52 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.1 Hz, 1 H); 5.18-5.09 (m, 3 H); 4.57 (s, 1 H); 4.42-4.37 (m, 2 H); 3.72-3.67 (m, 2 H); 3.46 (s, 2 H); 3.21-3.02 (m, 1 H); 2.81-2.50 (m, 10 H); 1.90 (s, 1 H); 1.79 (s, 1 H); 1.53 (s, 5 H); 1.34 (s, 1 H). formate 74C C (DMSO-d6): δ 8.29 (s, 1 H); 8.22 (d, J = 9.8 Hz, 1 H); 8.17 (d, J = 9.9 Hz, 1 H); 7.99 (d, J = 8.0 Hz, 2 H); 7.57 (d, J = 8.0 Hz, 2 H); 7.34-7.18 (m, 9 H); 7.09-7.01 (m, 2 H); 6.96-6.84 (m, 3 H); 6.49 (d, J = 9.9 Hz, 1 H); 5.81 (d, J = 9.3 Hz, 1 H); 5.33 (s, 2 H); 5.17 (s, 2 H); 5.05 (dd, J = 7.7, 4.7 Hz, 1 H); 4.56 (s, 1 H); 3.10 (m, 1 H); 2.89-2.70 (m, 10 H); 1.89 (br s, 2 H); 1.78 (br s, 2 H); 1.59 (br s, 1 H); 1.46 (br s, 1 H); 1.31 (br s, 1 H) formate 75C B (DMSO-d6): δ 8.40 (s, 1 H); 8.22 (d, J = 9.3 Hz, 1 H); 8.16 (d, J = 9.9 Hz, 1 H); 7.87 (d, J = 8.1 Hz, 2 H); 7.37-7.26 (m, 6 H); 7.26-7.18 (m, 2 H); 7.05 (d, J = 8.2 Hz, 1 H); 6.98-6.89 (m, 3 H); 6.82 (dd, J = 8.2, 2.4 Hz, 1 H); 6.49 (d, J = 9.9 Hz, 1 H); 5.84- .77 (m, 1 H); 5.01 (dd, J = 7.9, 4.5 Hz, 1 H); 4.59- 4.52 (m, 1 H); 4.40 (t, J = 6.2 Hz, 2 H); 4.10 (t, J = 6.2 Hz, 2 H); 3.12-3.02 (m, 1 H); 2.86-2.53 (m, 8 H); 2.20-2.11 (m, 2 H); 1.92-1.72 (m, 5 H); 1.63- 1.22 (m, 3 H). formate 76C A (DMSO-d6): δ 8.31 (s, 2 H); 8.28-8.14 (m, 2 H); 7.91 (d, J = 7.89 Hz, 2 H); 7.46 (d, J = 7.91 Hz, 2 H); 7.31 (d, J = 4.81 Hz, 4 H); 7.26-7.17 (m, 2 H); 7.10 (d, J = 8.15 Hz, 1 H); 6.98-6.87 (m, 3 H); 6.81 (d, J = 8.23 Hz, 1 H); 6.52 (d, J = 9.83 Hz, 1 H); .81 (d, J = 9.13 Hz, 1 H); 5.21-5.15 (m, 1 H); 4.59 (s, 2 H); 4.30-4.23 (m, 2 H); 4.19 (t, J = 6.64 Hz, 2 H); 3.13-3.07 (m, 3 H); 2.95-2.51 (m, 7 H); 1.92 (s, 1 H); 1.94-1.32 (m, 9 H). diformate (continued) 205 77C C (DMSO-d6): δ 8.41-8.12 (m, 3 H); 8.20-8.13 (m, 5 H); 7.35-7.23 (m, 5 H); 7.23-7.15 (m, 1 H); 7.13- 7.05 (m, 2 H); 7.05-6.91 (m, 3 H); 6.51 (d, J = 9.9 Hz, 1 H); 5.88-5.80 (m, 1 H); 5.60 (s, 2 H); 5.18- .11 (m, 1 H); 4.63-4.49 (m, 1 H); 4.36-4.29 (m, 2 H); 3.15-3.05 (m, 1 H); 2.86-2.71 (m, 7 H); 2.69- 2.49 (m, 2 H); 1.97-1.82 (m, 1 H); 1.81-1.72 (m, 3 H); 1.69-1.60 (m, 3 H); 1.60-1.33 (m, 1 H); 1.47- 1.20 (m, 1 H). diformate 78C C (CD3OD): δ 8.57 (s, 2 H); 8.38 (d, J = 9.9 Hz, 1 H); 8.01 (d, J = 8.0 Hz, 2 H); 7.48 (d, J = 8.0 Hz, 2 H); 7.35-7.19 (m, 7 H); 7.03 (d, J = 8.2 Hz, 1 H); 6.89- 6.79 (m, 3 H); 6.67 (d, J = 9.8 Hz, 1 H); 5.88 (s, 1 H); 5.39 (t, J = 6.7 Hz, 1 H); 4.89 (br s, 1 H); 4.51- 4.28 (m, 2 H); 3.80 (d, J = 5.5 Hz, 2 H); 3.65 (s, 2 H); 3.46 (m, 1 H); 3.18 (d, J = 6.7 Hz, 2 H); 3.24- 2.98 (m, 3 H); 3.09-2.89 (m, 5 H); 2.28-2.13 (m, 1 H); 2.19-2.07 (m, 3 H); 1.98-1.82 (m, 5 H); 1.91- 1.75 (m, 5 H); 1.88-1.45 (m, 1 H); 1.51-1.37 (m, 2 H) diformate 79C A (DMSO-d6): δ 8.31 (s, 2 H); 8.23 (d, J = 8.1 Hz, 1 H); 8.17 (d, J = 9.9 Hz, 1 H); 7.95 (d, J = 8.1 Hz, 2 H); 7.55 (d, J = 8.1 Hz, 2 H); 7.34-7.19 (m, 6 H); 7.08 (d, J = 8.2 Hz, 1 H); 7.02 (s, 1 H); 6.96-6.84 (m, 3 H); 6.51 (d, J = 9.9 Hz, 1 H); 5.81 (d, J = 9.2 Hz, 1 H); 5.17-5.08 (m, 3 H); 4.57 (s, 1 H); 4.42- 4.37 (m, 2 H); 3.70 (t, J = 4.6 Hz, 2 H); 3.46 (s, 2 H); 3.10 (m, 2 H); 2.79 (d, J = 6.3 Hz, 2 H); 2.75- 2.63 (m, 8 H); 1.84 (d, J = 44.6 Hz, 2 H); 1.53 (s, 5 H). diformate 80C A (DMSO-d6): δ 8.32 (s, 1 H); 8.25-8.12 (m, 2 H); 7.98 (d, J = 8.1 Hz, 2 H); 7.57 (d, J = 8.1 Hz, 2 H); 7.38-7.15 (m, 11 H); 7.09-6.98 (m, 2 H); 6.94-6.84 (m, 3 H); 6.50 (d, J = 9.9 Hz, 1 H); 5.81 (d, J = 9.4 Hz, 1 H); 5.32 (s, 2 H); 5.18 (s, 2 H); 5.03 (dd, J = 7.9, 4.6 Hz, 1 H); 4.55 (s, 1 H); 3.04 (m, 1 H); 2.83- 2.65 (m, 10 H); 1.94-1.83 (m, 1 H); 1.77 (s, 1 H); 1.56 (d, J = 11.1 Hz, 1 H); 1.45 (s, 1 H); 1.30 (s, 1 H) formate 81C C (CD3OD): δ 8.55 (s, 1 H); 8.33 (d, J = 9.9 Hz, 1 H); 7.95 (d, J = 8.1 Hz, 2 H); 7.46 (d, J = 8.0 Hz, 2 H); 7.35-7.18 (m, 8 H); 7.02-6.88 (m, 4 H); 6.64 (d, J = 9.8 Hz, 1 H); 5.88 (s, 1 H); 5.32 (dd, J = 9.0, 4.3 Hz, 1 H); 5.14 (s, 2 H); 4.80 (m, 1 H); 4.53-4.49 (m, 2 H); 3.91-3.86 (m, 2 H); 3.86-3.80 (m, 2 H); 3.22- 3.08 (m, 6 H); 3.01 (s, 3 H); 2.16 (d, J = 44.3 Hz, 2 H); 1.97-1.63 (m, 3 H). formate (continued) 206 82C C (DMSO-d6): δ 8.28 (s, 1 H); 8.23 (d, J = 9.8 Hz, 1 H); 8.17 (d, J = 9.9 Hz, 1 H); 7.81 (d, J = 8.0 Hz, 1 H); 7.62 (s, 1 H); 7.48 (d, J = 8.1 Hz, 1 H); 7.32-7.19 (m, 6 H); 7.09 (d, J = 8.2 Hz, 1 H); 7.03 (s, 1 H); 6.96-6.84 (m, 3 H); 6.51 (d, J = 9.9 Hz, 1 H); 5.82 (d, J = 9.2 Hz, 1 H); 5.18-5.06 (m, 3 H); 4.57 (s, 1 H); 4.29 (t, J = 6.3 Hz, 2 H); 3.10 (s, 2 H); 2.79 (d, J = 6.5 Hz, 2 H); 2.73 (t, J = 7.9 Hz, 4 H); 1.90 (s, 1 H); 1.76 (t, J = 10.9 Hz, 3 H); 1.66-1.57 (m, 4 H); 1.47 (s, 2 H); 1.33 (s, 1 H). formate 83C C (CD3OD): δ 8.55 (s, 2 H); 8.37 (d, J = 9.9 Hz, 1 H); 7.93 (t, J = 7.7 Hz, 1 H); 7.36-7.22 (m, 9 H); 7.03 (d, J = 8.2 Hz, 1 H); 6.95-6.86 (m, 3 H); 6.68 (d, J = 9.8 Hz, 1 H); 5.89 (s, 1 H); 5.40-5.34 (m, 1 H); 5.16 (s, 2 H); 4.95-4.79 (m, 1 H under solvent peak); 4.42 (s, 2 H); 3.56-3.42 (m, 1 H); 3.27- 3.01 (m, 9 H); 2.24 (s, 1 H); 2.12 (s, 1 H); 1.94 (s, 7 H). diformate Legend * NMR s = singlet; d = doublet; t = triplet; q = quartet; dd = doublet of doublets; m = multiplet; br = broad.
Biological characterization Example 83 M3 Receptor radioligand binding assay Human M3 receptor membranes (15ug/well) from Perkin Elmer were incubated with 0.52nM Scopolamine Methyl Chloride, [N-methyl-3H] with or without test compounds, or a saturating concentration of Atropine (5 µM) for the determination of non-specific binding. The assay was carried out in 96-well polypropylene plates in a volume of 250ul. The assay buffer used was 50mM Tris-HCl, 154mM NaCl (pH 7.4). The final assay concentration of DMSO was 0.5% (v/v). The plates were sealed and incubated for 2h at room temperature on an orbital shaker (slow speed). Membranes were harvested onto 96-well unifilter GF/C filter plates pre-treated with 0.5% polyethyleneimine (v/v), using a filter manifold, washed four times with 200ul of assay buffer. The plates were dried before addition of 50µl of microscint-0, 207 sealed then read in a Trilux Microbeta scintillation counter. IC50 values are determined from competition curves using a non-linear curve fitting program.
Ki values were calculated from IC50 values by the Cheng and Prusoff equation.
The Ki values of the tested compounds are less than 10 nM.
Example 84 β2 adrenoceptor radioligand binding assay Human β2 adrenoceptor membranes (7.5 ug/well) from Perkin Elmer were incubated with 0.3 nM 125-I Cyanopindolol with or without test compounds, or a saturating concentration of s-propranolol (2 µM) for the determination of non-specific binding. The assay was carried out in 96-well polypropylene plates in a volume of 200 ul. The assay buffer used was 25 mM HEPES, 0.5% BSA (w/v), 1 mM EDTA, 0.02% ascorbic acid (v/v), (pH 7.4).
The final assay concentration of DMSO was 0.5% (v/v). The plates were sealed and incubated for 1h at room temperature on an orbital shaker (slow speed). Membranes were harvested onto 96-well unifilter GF/C filter plates pre-treated with 0.5% polyethyleneimine (v/v), using a filter manifold, washed six times with 200 ul of wash buffer containing 10 mM HEPES and 500 mM NaCl. The plates were dried before addition of 50 µl of microscint-0, sealed then read in a Trilux Microbeta scintillation counter. IC50 values are determined from competition curves using a non-linear curve fitting program.
Ki values were calculated from IC50 values by the Cheng and Prusoff equation.
The Ki values of the tested compounds are less than 5 nM.
The term “comprising” as used in this specification and claims means “consisting at least in part of”. When interpreting statements in this specification, and claims which include the term “comprising”, it is to be understood that other features that are additional to the features prefaced by 208 this term in each statement or claim may also be present. Related terms such as “comprise” and “comprised” are to be interpreted in similar manner.
In this specification where reference has been made to patent specifications, other external documents, or other sources of information, this is generally for the purpose of providing a context for discussing the features of the invention. Unless specifically stated otherwise, reference to such external documents is not to be construed as an admission that such documents, or such sources of information, in any jurisdiction, are prior art, or form part of the common general knowledge in the art.
In the description in this specification reference may be made to subject matter that is not within the scope of the claims of the current application.
That subject matter should be readily identifiable by a person skilled in the art and may assist in putting into practice the invention as defined in the claims of this application.

Claims (25)

1. A compound of general formula I 5 wherein Q is a group of formula Q1, Q2, Q3, Q4, Q5 or Q6 10 Z is H or OH; Y is selected from Y’ and Y1 which are divalent groups of formula 15 Y or Y1 wherein 210 A1 and A2 are independently absent or are selected from the group consisting of (C1-C12)alkylene, (C3-C8)cycloalkylene and (C3-C8)heterocycloalkylene optionally substituted by one or more substituents selected from the group consisting of (C1-C6)alkyl, (C1-C6)arylalkyl and (C1-C6)heteroarylalkyl; 5 B is absent or is selected from the group consisting of (C3-C8)cycloalkylene, (C3-C8)heterocycloalkylene, arylene, heteroarylene or is a group of formula B1 optionally substituted by one or more groups selected from halogens, nitrile, 10 (C1-C6)alkyl, (C1-C6)alkoxy and (C1-C6)arylalkyl; C is absent or is selected from the group consisting of -O-, -CO-, -OC(O)-, -C(OO)-, -S-, -S(O)-, -S(O)2-, -N(R7)-, –N(CO)R7-, –N(CO)NHR7-, -N(SO2)R7- or is one of the following groups C1-C18 15 211 wherein R7 is H or is selected from the group consisting of linear or branched (C1-C8)alkyl, (C3-C8)cycloalkyl, (C3-C8)heterocycloalkyl, aryl, (C1-C6)arylalkyl, (C1-C6)alkoxy(C1-C6)alkyl and heteroaryl and R8 is 5 (C1-C8)alkoxycarbonyl; D is absent or is selected from the group consisting of (C1-C12)alkylene, -C(CH3)2-, arylene, (C2-C12)alkenylene, heteroarylene, (C3-C8)heterocycloalkylene and (C2-C6)alkynylene; n is 0 or an integer from 1 to 3; 10 E is absent or is selected from -O-, -NR7-, -OC(O)- and -S-; G is arylene or heteroarylene, optionally substituted by one or more substituents selected from the group consisting of halogen atoms, -OH, oxo (=O), -SH, -NO2, -CN, -CON(R6)2, -NH2, -NHCOR6, -CO2R6, (C1-C10)alkylsulfanyl, (C1-C10)alkylsulfinyl, (C1-C10)alkylsulfonyl, 15 (C1-C10)alkyl, aryl, haloaryl, heteroaryl and (C1-C10)alkoxy; R1 and R2 are independently H or selected from the group consisting of (C1-C8)alkyl, (C3-C8)cycloalkyl, (C3-C8)heterocycloalkyl, aryl, heteroaryl, aryl(C1-C6)alkyl, heteroaryl(C1-C6)alkyl and (C3-C8)cycloalkyl(C1-C6)alkyl, optionally substituted by one or more halogen atoms or (C1-C8)alkyl groups 20 or, taken together with the carbon atom to which they are bounded, R1 and R2 212 may form a (C3-C8)cycloalkyl, wherein R1 and R2 are not simultaneously H; M is -O- or -N(R3)-; R3 is H or is selected from the group consisting of (C1-C8)alkyl, (C3-C8)cycloalkyl, aryl and heteroaryl; 5 R4 is a group of formula J1, J2, J3, J4 or J5 R5 is a group of formula K 10 wherein p is 0 or an integer from 1 to 4; q is 0 or an integer from 1 to 4; P is absent or is selected from the divalent group consisting of O, S, SO, SO2, CO, NR6 CH=CH, N(R6)SO2, N(R6)COO, N(R6)C(O), SO2N(R6), CO(O)N(R6) and C(O)N(R6); 15 W is selected from the group consisting of H, (C1-C6)alkyl, (C3-C8)cycloalkyl, aryl and heteroaryl, optionally substituted by one or more substituents selected from the group consisting of halogen atoms, -OH, oxo (=O), -SH, -NO2, -CN, -CON(R6)2, -NH2, -NHCOR6, -CO2R6, (C1-C10)alkylsulfanyl, (C1-C10)alkylsulfinyl, (C1-C10)alkylsulfonyl, (C1-C10)alkyl and (C1-C10)alkoxy; X - 20 is a physiological acceptable anion; R6 is H or is selected from the group consisting of (C1-C10)alkyl, (C1-C6)haloalkyl, (C2-C6)alkynyl, (C2-C6)alkenyl, (C3-C8)cycloalkyl, (C3-C8)cycloalkyl(C1-C6)alkyl, heteroaryl and aryl optionally substituted by 213 one or more substituents selected from the group consisting of halogen atoms, -OH, oxo (=O), -SH, -NO2, -CN, -CONH2, -COOH, (C1-C10)alkoxycarbonyl, (C1-C10)alkylsulfanyl, (C1-C10)alkylsulfinyl, (C1-C10)alkylsulfonyl, (C1-C10)alkyl and (C1-C10)alkoxy; 5 and pharmaceutically acceptable salts or solvates thereof.
2. A compound according to claim 1, wherein B is absent or is selected from the group consisting of (C3-C8)cycloalkylene, (C3-C8)heterocycloalkylene, arylene and heteroarylene; C is absent or is selected from the group consisting of -O-, -CO-, -OC(O)-, -C(OO)-, -S-, 10 -S(O)-, -S(O)2-, and -N(R7)-, wherein R7 is H or is selected from the group consisting of (C1-C8)alkyl, (C3-C8)cycloalkyl, (C3-C8)heterocycloalkyl, aryl and heteroaryl; G is arylene or heteroarylene, optionally substituted by one or more substituents selected from the group consisting of halogen atoms, -OH, oxo (=O), -SH, -NO2, -CN, -CON(R6)2, -NH2, -NHCOR6, -CO2R6, 15 (C1-C10)alkylsulfanyl, (C1-C10)alkylsulfinyl, (C1-C10)alkylsulfonyl, (C1-C10)alkyl and (C1-C10)alkoxy and wherein Q, Z, A1, A2, D, E, G, R1, R2 M, R4 and R6 are as defined in claim 1.
3. A compound according to claim 2, wherein Q is Q1 20 Z is -OH, A1 is absent or is selected from the group consisting of (C3-C8)heterocycloalkylene and (C1-C12)alkylene, A2 is absent or (C1-C6)alkylene, B is absent or arylene, C is absent, D is absent or is selected from the group consisting of (C1-C12)alkylene, heteroarylene and arylene, E is 25 absent or is -O-, G is arylene optionally substituted by one or more halogen 214 atoms.
4. A compound according to claim 1, wherein A1 is absent or is selected from the group consisting of methylene, ethylene, propylene, butylene, pentylene, hexylene, heptylene, octylene and nonylene, A2 is absent or is 5 selected from the group consisting of methylene and oxadiazolene, B is selected from the group consisting of phenylene and cyclohexylene or is absent, C is absent, D is absent or is selected from methylene, ethylene, propylene, butylene, pentylene, hexylene, heptylene, octylene, nonylene, phenylene and oxadiazolene; G is selected from the group consisting of 10 fluoro-biphenylene and phenylene.
5. A compound according to claim 4, wherein A1 is selected from the group consisting of ethylene, pentylene, hexylene, heptylene, octylene and nonylene, D is absent, R1 is H, R2 is selected from the group consisting of phenyl, biphenyl, naphthyl, pyridinyl, difluorophenyl, methylphenyl, 15 fluorophenyl and thiophenyl, M is -N(H)-, R4 is a group of formula J1 or J3 20 or J4 215 or J5 wherein R5 is a group of formula K, wherein p is 0 or 1, P is absent or is CO, 5 q is absent or is 1 and W is H or is selected from the group consisting of (C1-C6)alkyl and aryl.
6. A compound according to claim 2, wherein Q is Q3 Z is H, A1 is absent or is (C1-C12)alkylene, A2 is absent, B is absent, C is 10 absent, D is absent or (C1-C12)alkylene, E is -O-, G is arylene.
7. A compound according to claim 6, wherein A1 is absent or is selected from the group consisting of methylene, ethylene, propylene, butylene, pentylene, hexylene, heptylene, octylene and nonylene, A2 is absent, B is absent, C is absent, D is absent or is selected from methylene, ethylene, 15 propylene, butylene, pentylene, hexylene, heptylene, octylene and nonylene; G is phenylene.
8. A compound according to claim 1, wherein R1 and R2 are independently H or selected from the group consisting of (C1-C8)alkyl, (C3-C8)cycloalkyl, (C3-C8)heterocycloalkyl, aryl, heteroaryl, aryl(C1-C6)alkyl, heteroaryl(C1- 216 C6)alkyl and (C3-C8)cycloalkyl(C1-C6)alkyl, optionally substituted by one or more halogen atoms or (C1-C8)alkyl groups or, taken together with the carbon atom they are linked to, R1 and R2 may form a (C3-C8)cycloalkyl group, wherein R1 and R2 are not simultaneously H; M is -O- or -N(R3)-; R3 is H or 5 is selected from the group consisting of (C1-C8)alkyl, (C3-C8)cycloalkyl, aryl and heteroaryl; R4 is a group of formula J1, J2, J3, J4 or J5 R5 is a group of formula K 10 wherein p is 0 or an integer from 1 to 4; q is 0 or an integer from 1 to 4; P is absent or is selected from the group consisting of -O-, -S-, -S(O)-, -S(O2)-, -C(O)-, -N(R6)-, -CH=CH-, -N(R6)S(O2)-, -N(R6)CO(O)-, -N(R6)C(O)-, -SO2N(R6)-, -CO(O)N(R6)- and -C(O)N(R6)-; W is selected from the group 15 consisting of (C1-C6)alkyl, (C3-C8)cycloalkyl, aryl and heteroaryl, optionally substituted by one or more substituents selected from the group consisting of halogen atoms, -OH, oxo (=O), -SH, -NO2, -CN, -CON(R6)2, -NH2, -NHCOR6, -CO2R6, (C1-C10)alkylsulfanyl, (C1-C10)alkylsulfinyl, (C1-C10)alkylsulfonyl, (C1-C10)alkyl and (C1-C10)alkoxy; R6 is selected from the group consisting of 20 H, (C1-C10)alkyl, (C1-C6)haloalkyl, (C3-C8)cycloalkyl, heteroaryl and aryl; G, Y, Z and Q are as defined in claim 1.
9. A compound according to claim 8, wherein R1 and R2 are independently H or selected from the group consisting of (C1-C8)alkyl, 217 (C3-C8)cycloalkyl, aryl and heteroaryl, optionally substituted by one or more halogen atoms or (C1-C8)alkyl groups or, taken together with the carbon atom to which they are bounded, R1 and R2 may form a (C3-C8)cycloalkyl group, wherein R1 and R2 are not simultaneously H; M is -N(R3)-; R3 is H; R4 is a 5 group of formula J1 or J3 or J4 10 wherein R5 is a group of formula K, wherein p is 0, P is absent, q is 1 and W is selected from the group consisting of (C1-C6)alkyl and aryl.
10. A compound according to claim 9, wherein W is H or phenyl; R1 is H, R2 is selected from the group consisting of phenyl, biphenyl, naphthyl, 15 thiophenyl, pyridinyl, difluorophenyl, methylphenyl and fluorophenyl; M is -N(H)-; R4 is selected from the group consisting of quinuclidinyl, benzylpiperidinyl, methylpiperidinyl, benzylazabicyclo[3.2.1]octanyl and azoniabicyclo[2.2.2]octanyl. 218
11. A compound according to claim 1, wherein Q is a group of formula Q1, Q2, Q3, Q4, Q5 or Q6, Z is H or OH; Y1 is a group of formula 5 Y1 wherein A1 is (C1-C12)alkylene; C is absent or is selected from the group consisting of -O-, -CO-, -OC(O)- or is a group of formula C1-C18 wherein R7 is H or is selected from the group consisting of linear or branched (C1-C8)alkyl, (C3-C8)cycloalkyl, (C3-C8)heterocycloalkyl, aryl, (C1-C6)arylalkyl, (C1-C6)alkoxy(C1-C6)alkyl and heteroaryl and R8 10 is (C1-C8)alkoxycarbonyl; B is absent or is selected from the group consisting of (C3-C8)cycloalkylene and arylene; D is absent or is selected from the group consisting of (C1-C12)alkylene, -C(CH3)2-, heteroarylene and arylene; n is 0 or an integer from 1 to 2; E is -O-; G is arylene or heteroarylene, optionally 15 substituted by one or more substituents selected from the group consisting of halogen atoms, -OH, oxo (=O), -SH, -NO2, -CN, -CON(R6)2, -NH2, -NHCOR6, -CO2R6, (C1-C10)alkylsulfanyl, (C1-C10)alkylsulfinyl, (C1-C10)alkylsulfonyl, (C1-C10)alkyl, aryl, haloaryl, heteroaryl and (C1-C10)alkoxy; R1, R2, M and R4 are as defined in claim 1. 20
12. A compound according to claim 11, wherein A1 is selected from the group consisting of methylene, ethylene, propylene, butylene, pentylene and hexylene; C is absent or is selected from the group consisting of -O-, -CO-, -OC(O)-, C11, C13, C14, C16, C17, C18 wherein R7 is H or is selected from the group consisting of methyl, ethyl and isopropyl and C15 wherein n is 0 or 1 and R8 25 is ethoxycarbonyl; B is absent or is selected from phenylene, cyclopropylene, cyclohexylene, optionally substituted by one or more halogens; D is absent or is selected from methylene, -C(CH3)2-, phenylene and oxadiazolylene; n is 0 or an integer from 1 to 2; E is -O-; G is selected from 219 phenylene and biphenylene, optionally substituted by one or more substituents selected from the group consisting of fluorine, phenyl and 2-thiophenyl.
13. A compound according to claim 1, which is (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(phenyl)methylcarbamate; 5 (R)-quinuclidinyl (3-(8-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)octyloxy)phenyl)(phenyl)methylcarbamate; (R)-quinuclidinyl(3-(7-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)heptyloxy)phenyl)(phenyl)methylcarbamate; (R)-quinuclidinyl (3-(6-((R)hydroxy(8-hydroxyoxo-1,2- 10 dihydroquinolinyl)ethylamino)hexyloxy)phenyl)(phenyl)methylcarbamate; (R)-quinuclidinyl (3-(5-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)pentyloxy)phenyl)(phenyl)methylcarbamate; 1-benzylpiperidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(phenyl)methylcarbamate; 15 1-methylpiperidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(phenyl)methylcarbamate; 8-benzylazabicyclo[3.2.1]octanyl (3-(9-((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolin yl)ethylamino)nonyloxy)phenyl)(phenyl)methylcarbamate; 20 (R)-quinuclidinyl (4-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(phenyl)methylcarbamate; (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(thiophen yl)methylcarbamate; 25 (R)-quinuclidinyl biphenylyl(3-(9-((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethylamino)nonyloxy)phenyl)methylcarbamate; (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- 220 dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(naphthalen yl)methylcarbamate; (R)-quinuclidinyl biphenylyl(3-(9-((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethylamino)nonyloxy)phenyl)methylcarbamate; (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- 5 dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(pyridin yl)methylcarbamate; (R)-quinuclidinyl (3,5-difluorophenyl)(3-(9-((R)hydroxy(8-hydroxy2-oxo-1,2-dihydroquinolin yl)ethylamino)nonyloxy)phenyl)methylcarbamate; 10 (R)-quinuclidinyl (3,4,5-difluorophenyl)(3-(9-((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)nonyloxy)phenyl)methylcarbamate (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(o-tolyl)methylcarbamate; 15 (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(m-tolyl)methylcarbamate; (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(p-tolyl)methylcarbamate; (R)-quinuclidinyl (4-difluorophenyl)(3-(9-((R)hydroxy(8-hydroxy 20 oxo-1,2-dihydroquinolinyl)ethylamino)nonyloxy)phenyl)methylcarbamate; (R)-quinuclidinyl (3-fluorophenyl)(3-(9-((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethylamino)nonyloxy)phenyl)methylcarbamate; (R)-quinuclidinyl (3-chlorophenyl)(3-(9-((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethylamino)nonyloxy)phenyl)methylcarbamate; 25 (R)-quinuclidinyl (cyclohexyl(3-((9-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)methyl)carbamate; (R)-quinuclidinyl ((3-((6-(((R)hydroxy(8-hydroxyoxo-1,2- 221 dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(thiophen yl)methyl)carbamate; (R)-quinuclidinyl ((3-((6-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)(thiophen yl)methyl)carbamate 5 (R)-quinuclidinyl (3-(9-(2-(4-hydroxyoxo-2,3-dihydrobenzo[d]thiazol yl)ethylamino)nonyloxy)phenyl)(phenyl)methylcarbamate; (R)-quinuclidinyl (3-(4-(2-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin yl)ethylamino)ethyl)benzyloxy)phenyl)(phenyl)methylcarbamate; 10 (R)-quinuclidinyl (3-(2-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)ethyl)phenyl)(phenyl)methylcarbamate; (3R)((3-(6-((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyloxy)phenyl)(phenyl)methylcarbamoyloxy)(2-oxo phenylethyl)azoniabicyclo[2.2.2]octane; 15 (R)-quinuclidinyl (3-(3-(2-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin yl)ethylamino)ethyl)benzyloxy)phenyl)(phenyl)methylcarbamate formate; (3R)((((3-((4-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin5-yl)ethyl)amino)ethyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy) 20 (2-oxophenylethyl)quinuclidinium; (3R)((((3-chlorophenyl)(3-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)methyl)carbamoyl)oxy)- 1-(2-oxophenylethyl)quinuclidinium; (3R)((((3-bromo((9-(((R)hydroxy(8-hydroxyoxo-1,2- 25 dihydroquinolin yl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)(2-oxo phenylethyl)quinuclidinium; 222 (R)-quinuclidinyl (2-chloro(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)phenyl)(phenyl)methylcarbamate; (R)-quinuclidinyl ((2,6-difluoro((9-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolin yl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)carbamate; 5 (R)-quinuclidinyl ((2-bromo((9-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolin yl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)carbamate; (3R)((((2-chloro((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin 10 yl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)(2-oxo phenylethyl)quinuclidinium; (3R)((((2,6-difluoro((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin yl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)(2-oxo 15 phenylethyl)quinuclidinium; (3R)((((2-bromo((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin yl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)(2-oxo phenylethyl)quinuclidinium; 20 (3R)((((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)nonyl)oxy)methylphenyl)(phenyl)methyl)carbamoyl)oxy)- 1-(2-oxophenylethyl)quinuclidinium; (R)-quinuclidinyl ((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy) 25 methoxyphenyl)(phenyl)methyl)carbamate; (R)-quinuclidinyl ((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy) 223 methoxyphenyl)(phenyl)methyl)carbamate; (3R)((((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)nonyl)oxy)methoxyphenyl)(phenyl)methyl)carbamoyl)oxy)- 1-(2-oxophenylethyl)quinuclidinium; (3R)((((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 5 yl)ethyl)amino)nonyl)oxy)methoxyphenyl)(phenyl)methyl)carbamoyl)oxy)- 1-(2-oxophenylethyl)quinuclidinium; (3R)((((5-((9-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)nonyl)oxy)-[1,1'-biphenyl] yl)(phenyl)methyl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium; 10 (R)-quinuclidinyl (3-(9-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)nonyloxy)(thiophen yl)phenyl)(phenyl)methylcarbamate; (3R)((((3-((3-(4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin5-yl)ethyl)amino)butoxy)benzyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)- 15 1-(2-oxophenylethyl)quinuclidinium; (3R)((((3-((3-(4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin5-yl)ethyl)amino)butoxy)benzyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)- 1-(2-phenoxyethyl)quinuclidinium; (3R)((((3-((3-((5-(((R)hydroxy(8-hydroxyoxo-1,2- 20 dihydroquinolin yl)ethyl)amino)pentyl)oxy)benzyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)- 1-(2-oxophenylethyl)quinuclidinium; (3R)((((3-((3-((5-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin 25 yl)ethyl)amino)pentyl)oxy)benzyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)- 1-(2-phenoxyethyl)quinuclidinium; (R)-quinuclidinyl (3-fluorophenyl)(3-(6-((R)hydroxy(8-hydroxy 224 oxo-1,2-dihydroquinolinyl)ethylamino)hexyloxy)phenyl)methylcarbamate; (3R)((((3-((5-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)(4- phenylbutyl)quinuclidinium; (R)-Quinuclidinyl (3-fluorophenyl)(3-(3-(2-((R)hydroxy(8-hydroxy5 2-oxo-1,2-dihydroquinolin yl)ethylamino)ethyl)benzyloxy)phenyl)methylcarbamate; (3R)((((3-fluorophenyl)(3-((3-(2-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin yl)ethyl)amino)ethyl)benzyl)oxy)phenyl)methyl)carbamoyl)oxy)(2-oxo 10 phenylethyl)quinuclidinium; (3R)((((3-((4-((((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)methyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy) (2-oxophenylethyl)quinuclidinium; (R)-Quinuclidinyl (3-((4'-(2-((R)hydroxy(8-hydroxyoxo-1,2- 15 dihydroquinolinyl)ethylamino)ethyl)biphenyl yl)methoxy)phenyl)(phenyl)methylcarbamate; (R)-quinuclidinyl ((3-((4-((4-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin yl)ethyl)amino)butyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate; 20 (R)-quinuclidinyl (3-(4-(3-((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin yl)ethylamino)propylcarbamoyl)benzyloxy)phenyl)(phenyl)methylcarbamate; (3R)((((3-((4-((3-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin 25 yl)ethyl)amino)propyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamo yl)oxy)(2-oxophenylethyl)quinuclidinium; 4-(((R)Hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 225 yl)ethyl)amino)butyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 5-((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)pentyl 4-((3-(phenyl(((R)-quinuclidin yloxy)carbonylamino)methyl)phenoxy)methyl)benzoate; 5 6-((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyl 4-((3-(phenyl(((R)-quinuclidin yloxy)carbonylamino)methyl)phenoxy)methyl)benzoate; 7-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)heptyl 4-((3-(phenyl((((R)-quinuclidin 10 yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 4-((((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)methyl)benzyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 4-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 15 yl)ethyl)amino)ethyl)phenyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 4-((((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)methyl)phenyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate 20 4-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethyl)benzyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; (3R)((((3-((4-(1-((4-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin 25 yl)ethyl)amino)butoxy)carbonyl)cyclopropyl)benzyl)oxy)phenyl)(phenyl)meth yl)carbamoyl)oxy)(2-oxophenylethyl)quinuclidinium; (R)-quinuclidinyl (3-(2-(3'-(((R)hydroxy(8-hydroxyoxo-1,2- 226 dihydroquinolinyl)ethylamino)methyl)biphenyl yl)ethoxy)phenyl)(phenyl)methylcarbamate; (R)-quinuclidinyl (3-(2-(3'-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethylamino)methyl)biphenyl yl)ethoxy)phenyl)(phenyl)methylcarbamate; 5 6-((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethylamino)hexyl 2-(3-(phenyl(((R)-quinuclidin yloxy)carbonylamino)methyl)phenoxy)acetate; (R)-quinuclidinyl ((3-((6-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin 10 yl)ethyl)amino)hexyl)oxy)phenyl)(phenyl)methyl)carbamate; (R)-quinuclidinyl ((3-((6-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin yl)ethyl)amino)hexyl)oxy)phenyl)(phenyl)methyl)carbamate; (3R)((((3-((6-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 15 yl)ethyl)amino)hexyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)(2-oxo phenylethyl)quinuclidinium; (3R)((((3-((6-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)hexyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)(2-oxo phenylethyl)quinuclidinium; 20 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-((3-(phenyl((((R)-quinuclidin 25 yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 5-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl 2-(3-(phenyl((((R)-quinuclidin 227 yloxy)carbonyl)amino)methyl)phenoxy)acetate; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)acetate; 5-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 5 yl)ethyl)amino)pentyl 2-methyl(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)propanoate; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-methyl(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)propanoate; 10 5-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl 2,2-dimethyl(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)propanoate; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 1-(2-(3-(phenyl((((R)-quinuclidin 15 yloxy)carbonyl)amino)methyl)phenoxy)acetyl)piperidinecarboxylate; 4-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethyl)benzyl 2-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)acetate; (R)-quinuclidinyl ((3-((9-(((R)hydroxy(8-hydroxyoxo-1,2- 20 dihydroquinolinyl)ethyl)amino)nonyl)oxy) methylphenyl)(phenyl)methyl)carbamate; (R)-Quinuclidinyl ((3-bromo((9-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolin yl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)carbamate; 25 (R)-quinuclidinyl ((5-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)-[1,1'-biphenyl] yl)(phenyl)methyl)carbamate; 228 (R)-quinuclidinyl ((2-bromo((9-(((R)hydroxy(8-hydroxyoxo1,2-dihydroquinolin yl)ethyl)amino)nonyl)oxy)phenyl)(phenyl)methyl)carbamate; (R)-quinuclidinyl ((3'-fluoro((9-(((R)hydroxy(8-hydroxyoxo5 1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)-[1,1'-biphenyl] yl)(phenyl)methyl)carbamate; (R)-quinuclidinyl ((3-((3-(4-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin yl)ethyl)amino)butoxy)benzyl)oxy)phenyl)(phenyl)methyl)carbamate; 10 (R)-quinuclidinyl ((3-((3-((5-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin yl)ethyl)amino)pentyl)oxy)benzyl)oxy)phenyl)(phenyl)methyl)carbamate; (3R)(((cyclohexyl(3-((9-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)nonyl)oxy)phenyl)methyl)carbamoyl)oxy)- 15 1-(2-oxophenylethyl)quinuclidinium; (3R)((((3-((6-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)hexyl)oxy)phenyl)(thiophenyl)methyl)carbamoyl)oxy) (2-oxophenylethyl)quinuclidinium; (3R)((((3-fluorophenyl)(3-((6-(((R)hydroxy(8-hydroxyoxo-1,2- 20 dihydroquinolinyl)ethyl)amino)hexyl)oxy)phenyl)methyl)carbamoyl)oxy)- 1-(2-oxophenylethyl)quinuclidinium; (3R)((((3-((6-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)hexyl)oxy)phenyl)(thiophenyl)methyl)carbamoyl)oxy) (2-oxophenylethyl)quinuclidinium; 25 (3R)((((3-((4-((4-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin yl)ethyl)amino)butyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamoy l)oxy)(2-oxophenylethyl)quinuclidinium; 229 (3R)((((3-((7-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)heptyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)(2-oxo2-phenylethyl)quinuclidinium; (3R)((((3-((7-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 5 yl)ethyl)amino)heptyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)(3- phenylpropyl)quinuclidinium; (3R)((((3-((5-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl)oxy)phenyl)(phenyl)methyl)carbamoyl)oxy)(2-oxo2-phenylethyl)quinuclidinium; 10 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 1-(4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)phenyl)cyclopentanecarboxylate; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 1-(4-((3-(phenyl((((R)-quinuclidin 15 yloxy)carbonyl)amino)methyl)phenoxy)methyl)phenyl)cyclohexanecarboxylate; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-methyl(4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)phenyl)propanoate; 8-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 20 yl)ethyl)amino)octyl 3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzoate; 9-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)nonyl 3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzoate; 25 7-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)heptyl 3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzoate; 6-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 230 yl)ethyl)amino)hexyl 3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzoate; 5-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl 3-(phenyl((((R)-quinuclidin 5 yloxy)carbonyl)amino)methyl)benzoate; 4-((4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl)carbamoyl)benzyl 3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzoate; 4-(N-(4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 10 yl)ethyl)amino)butyl)sulfamoyl)benzyl 3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzoate; 4-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethyl)benzyl 3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzoate; 15 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)benzamido)methyl)benzoate; (2S)(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 3-phenyl(4-((3-(phenyl((((R)-quinuclidin 20 yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzamido)propanoate; (R)-quinuclidinyl ((3-((3-(4-(2-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolinyl)ethyl)amino)ethyl)phenyl)-1,2,4-oxadiazol yl)methoxy)phenyl)(phenyl)methyl)carbamate; (R)-quinuclidinyl ((5-((9-(((R)hydroxy(8-hydroxyoxo-1,2- 25 dihydroquinolinyl)ethyl)amino)nonyl)oxy)pyridin yl)(phenyl)methyl)carbamate; (R)-quinuclidinyl ((3-fluorophenyl)(5-((9-(((R)hydroxy(8-hydroxy oxo-1,2-dihydroquinolinyl)ethyl)amino)nonyl)oxy)pyridin 231 yl)methyl)carbamate; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-chloro((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 5 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-fluoro((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 6-((3-(phenyl((((R)-quinuclidin 10 yloxy)carbonyl)amino)methyl)phenoxy)methyl)nicotinate; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 5-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)furancarboxylate 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 15 yl)ethyl)amino)butyl 2-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)oxazolecarboxylate 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 3-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 20 5-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl 2-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)acetate; 5-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl 2-(3-(phenyl((((R)-quinuclidin 25 yloxy)carbonyl)amino)methyl)phenoxy)acetate; 5-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)hexyl 2-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)acetate; 232 5-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)hexyl 2-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)acetate; (R)-quinuclidinyl ((3-((4-((3-(((R)hydroxy(8-hydroxyoxo-1,2- 5 dihydroquinolin yl)ethyl)amino)propyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate; (R)-quinuclidinyl ((3-((4-((3-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin yl)ethyl)amino)ethyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate; 10 (R)-quinuclidinyl ((3-((4-(ethyl(3-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin yl)ethyl)amino)propyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl)carbamate; (R)-quinuclidinyl ((3-((4-((3-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin 15 yl)ethyl)amino)propyl)(methyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)methyl) carbamate; (R)-quinuclidinyl ((3-((4-((3-(((R)hydroxy(8-hydroxyoxo-1,2- dihydroquinolin yl)ethyl)amino)propyl)(isopropyl)carbamoyl)benzyl)oxy)phenyl)(phenyl)meth 20 yl)carbamate; (1R,4R)(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-((4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzamido)methyl)cyclohexan ecarboxylate; 25 (2S)-methyl 4-((2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin5-yl)ethyl)amino)ethyl)(methyl)amino)oxo(4-((3-(phenyl((((R)- quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzamido)butanoate; 233 ((1R,4R)((((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)methyl)cyclohexyl)methyl 4-((3-(phenyl(((quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 2-((4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 5 yl)ethyl)amino)butyl)amino)oxoethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 2-((3-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)propyl)amino)oxoethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 10 2-(4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butoxy)oxoethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 2-((5-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl)oxy)oxoethyl 4-((3-(phenyl((((R)-quinuclidin 15 yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 2-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethoxy)ethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 2-(4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 20 yl)ethyl)amino)butoxy)ethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 2-((5-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)pentyl)oxy)oxoethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 25 2-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethoxy)ethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 2-(4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 234 yl)ethyl)amino)butoxy)ethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 3-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethyl)benzyl 4-((3-(phenyl((((R)-quinuclidin 5 yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 3-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)propyl 4-(2-(((R)hydroxy(8- hydroxyoxo-1,2-dihydroquinolinyl)ethyl)amino)ethyl)benzoate; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 10 yl)ethyl)amino)butyl 4-(2-(3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)ethyl)benzoate; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-(5-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)-1,2,4-oxadiazol 15 yl)benzoate; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 4-((4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)piperidin yl)methyl)benzoate; 20 2-(4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butoxy)ethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 4-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethyl)benzyl 4-((3-(phenyl((((R)-quinuclidin 25 yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 2-(2-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)ethoxy)ethyl 4-((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 235 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin yl)ethyl)amino)butyl 2-chloro((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate; 4-(((R)hydroxy(8-hydroxyoxo-1,2-dihydroquinolin 5 yl)ethyl)amino)butyl 2-fluoro((3-(phenyl((((R)-quinuclidin yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate.
14. A pharmaceutical composition comprising a compound of formula I as defined in any one of the claims 1-13, with one or more pharmaceutically acceptable carriers and/or excipients. 10
15. Use of a compound of any one of claims 1-13 in the manufacture of a medicament.
16. Use of a compound of formula I according to any one of claims 1-13 for the manufacture of a medicament for the prevention and/or treatment of broncho-obstructive or inflammatory diseases. 15
17. A use as claimed in claim 16 for treating asthma, chronic bronchitis or chronic obstructive pulmonary disease (COPD).
18. A combination of a compound of formula I as defined in any one of the claims 1-13 with one or more active ingredients selected from the classes consisting of corticosteroids, P38 MAP kinase inhibitors, IKK2 inhibitors, 20 HNE inhibitors, PDE4 inhibitors, leukotriene modulators, NSAIDs and mucus regulators.
19. A pharmaceutical composition according to claim 14 to be administered by inhalation, such as inhalable powders, propellant-containing metering aerosols or propellant-free inhalable formulations. 25
20. A device comprising the pharmaceutical composition according to claim 19, which may be a single- or multi-dose dry powder inhaler, a metered dose inhaler and a soft mist nebulizer. 236
21. A compound of general formula I as claimed in claim 1, substantially as herein described with reference to any example thereof.
22. A pharmaceutical composition as claimed in claim 14, substantially as herein described with reference to any example thereof. 5
23. A use as claimed in claims 15 or 16, substantially as herein described with reference to any example thereof.
24. A combination as claimed in claim 18, substantially as herein described with reference to any example thereof.
25. A device as claimed in claim 20, substantially as herein described with 10 reference to any example thereof.
NZ618727A 2011-06-10 2012-06-07 Compounds having muscarinic receptor antagonist and beta2 adrenergic receptor agonist activity NZ618727B2 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
EP11169537.5 2011-06-10
EP11169537 2011-06-10
EP12165283 2012-04-24
EP12165283.8 2012-04-24
PCT/EP2012/060795 WO2012168359A1 (en) 2011-06-10 2012-06-07 Compounds having muscarinic receptor antagonist and beta2 adrenergic receptor agonist activity

Publications (2)

Publication Number Publication Date
NZ618727A NZ618727A (en) 2016-01-29
NZ618727B2 true NZ618727B2 (en) 2016-05-03

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