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WO2023016527A1 - Classe de composés spiro de benzoxazine et procédé de préparation correspondant - Google Patents

Classe de composés spiro de benzoxazine et procédé de préparation correspondant Download PDF

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Publication number
WO2023016527A1
WO2023016527A1 PCT/CN2022/111883 CN2022111883W WO2023016527A1 WO 2023016527 A1 WO2023016527 A1 WO 2023016527A1 CN 2022111883 W CN2022111883 W CN 2022111883W WO 2023016527 A1 WO2023016527 A1 WO 2023016527A1
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Prior art keywords
compound
reaction solution
alkyl
added
mmol
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English (en)
Chinese (zh)
Inventor
吴凌云
赵乐乐
孙建军
贾海飞
黎健
陈曙辉
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Medshine Discovery Inc
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Medshine Discovery Inc
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/538—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with carbocyclic ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/10—Spiro-condensed systems

Definitions

  • the invention relates to a class of benzoxazine spiro compounds, a preparation method thereof, and the application of the compounds in the preparation of medicines for treating related diseases. It specifically relates to the compound represented by formula (I) and its pharmaceutically acceptable salt.
  • Tumor immunotherapy is a therapeutic area that has attracted much attention in recent years.
  • the main mechanism is to enhance the anti-tumor ability of the immune microenvironment by mobilizing the body's immune system.
  • monoclonal antibody drugs for tumor immunotherapy such as Keytruda and OPDIVO, have been used for the treatment of various cancers such as non-small cell lung cancer and melanoma.
  • RORs Retinoic acid-related orphan receptors
  • RORs Retinoic acid-related orphan receptors
  • RORs belong to the nuclear receptor superfamily and are a member of intracellular transcription factors, which can regulate a variety of physiological processes, including reproductive development, metabolism, and immune system regulation.
  • ROR has three family members: ROR- ⁇ , - ⁇ and - ⁇ , which are encoded by RORA, RORB and RORC genes, respectively.
  • ROR ⁇ includes two subtypes, ROR ⁇ 1 and ROR ⁇ t (ROR ⁇ 2).
  • ROR ⁇ 1 is expressed in various tissues and organs such as thymus, muscle, pancreas, prostate, and liver, while the short-chain subtype ROR ⁇ t of ROR ⁇ is mainly distributed in the thymus and promotes the differentiation of initial T cells into Th17 and Tc17 cells.
  • Th17 and Tc17 cells promote inflammatory and autoimmune responses by secreting IL-17, IL-22, GM-CSF and other cytokines and inflammatory factors.
  • IL-17 can promote the recruitment and infiltration of CTLs and NK cells in the tumor microenvironment, and enhance the anti-tumor effect of effector T cells.
  • ROR ⁇ agonists currently have no drugs approved for marketing, and Lycera Corp’s
  • ROR ⁇ agonist LYC-55716 monotherapy for the treatment of advanced solid tumors is in phase II clinical research, and it is combined with PD-1 monoclonal antibody pembrolizumab in the treatment of advanced non-small cell lung cancer The treatment is in a phase 1b clinical study.
  • this field still needs candidate compounds with better activity and better pharmacokinetic parameters to advance to clinical trials to meet the therapeutic needs.
  • the present invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof,
  • R 11 , R 12 , R 13 , R 14 and R 15 are independently selected from H, F, Cl, Br, I, -OH, -NH 2 , -CN, C 1-3 alkyl, C 1-3 Alkoxy and C 1-3 alkylamino, wherein said C 1-3 alkyl, C 1-3 alkoxy and C 1-3 alkylamino are independently optionally substituted by 1, 2 or 3 R a ;
  • R 2 is selected from C 1-6 alkyl and -C 1-3 alkyl-C 3-4 cycloalkyl, said C 1-6 alkyl and -C 1-3 alkyl-C 3-4 cycloalkane
  • the groups are independently optionally substituted by 1, 2 or 3 R b ;
  • L is selected from a single bond, -C 2-4 alkenyl- and -4-5 membered heterocycloalkyl-, and the -C 2-4 alkenyl- and -4-5 membered heterocycloalkyl- are independently optionally substituted by 1, 2 or 3 R c ;
  • R a is independently selected from F, Cl, Br, I, -OH, -NH 2 and C 1-3 alkyl, wherein the C 1-3 alkyl is optionally substituted by 1, 2 or 3 R;
  • R b are independently selected from F, Cl, Br, I, -OH, -NH 2 , -CN, -COOH and C 1-3 alkyl;
  • R c are independently selected from F, Cl, Br, I, -OH, -NH 2 , -CN, -COOH and C 1-3 alkyl;
  • R is independently selected from F, Cl, Br, I, -OH and -NH 2 ;
  • Hetero in the -4-5 membered heterocycloalkyl- means 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from -O-, -NH-, -S- and N, respectively.
  • R a is selected from F, Cl, Br, I, -OH, -NH 2 and -CH 3 , and other variables are as defined in the present invention.
  • R a is selected from F, and other variables are as defined in the present invention.
  • R b is selected from F, Cl, Br, I, -OH, -NH 2 , -CN, -COOH and -CH 3 , and other variables are as defined in the present invention.
  • R b is selected from -COOH, and other variables are as defined in the present invention.
  • R b is selected from -CH 3 , and other variables are as defined in the present invention.
  • R c is selected from F, Cl, Br, I, -OH, -NH 2 , -CN, -COOH and -CH 3 , and other variables are as defined in the present invention.
  • R c is selected from -CH 3 , and other variables are as defined in the present invention.
  • R 11 , R 12 , R 13 , R 14 and R 15 are independently selected from H, F, Cl, Br, I, -OH, -NH 2 , -CN, -CH 3 , -O-CH 3 and -NH-CH 3 , wherein said -CH 3 , -O-CH 3 and -NH-CH 3 are independently optionally substituted by 1, 2 or 3 R a , R a and Other variables are as defined herein.
  • R 11 , R 12 , R 13 , R 14 and R 15 are selected from H, F, Cl, Br, I, -OH, -NH 2 , -CN, -CH 3 , -CF 3 , -O-CH 3 , -O-CH 2 F, -O-CHF 2 , -O-CF 3 and Other variables are as defined herein.
  • R 11 is selected from H, Cl and -O-CH 3 , and other variables are as defined in the present invention.
  • R 12 is selected from H and F, and other variables are as defined in the present invention.
  • R 13 is selected from H, and other variables are as defined in the present invention.
  • R 14 is selected from H and -O-CH 3 , wherein the -O-CH 3 is optionally substituted by 1, 2 or 3 R a , and R a and other variables are as described in the present invention definition.
  • R 14 is selected from H and -O-CHF 2 , and other variables are as defined in the present invention.
  • the above-mentioned R 15 is selected from H, F and -CH 3 , wherein the -CH 3 is optionally substituted by 1, 2 or 3 R a , and R a and other variables are as defined in the present invention.
  • R 15 is selected from H, F and -CF 3 , and other variables are as defined in the present invention.
  • R 2 is selected from C 1-4 alkyl and -C 1-3 alkyl-cyclopropyl, wherein the C 1-4 alkyl and -C 1-3 alkyl-cyclopropyl
  • the propyl groups are each independently optionally substituted by 1, 2 or 3 R b , and R b and other variables are as defined in the present invention.
  • R 2 is selected from -CH 3 , -CH 2 -CH 3 , -CH 2 -CH 2 -CH 3 , Wherein -CH 3 , -CH 2 -CH 3 , -CH 2 -CH 2 -CH 3 , are independently and optionally substituted by 1, 2 or 3 R b , and R b and other variables are as defined in the present invention.
  • the above-mentioned L is selected from single bonds, -C 2-3 alkenyl- and -azetidinyl-, wherein the -C 2-3 alkenyl- and -azetidinyl-are independently optionally Substituted by 1, 2 or 3 Rc , Rc and other variables are as defined herein.
  • the present invention also provides the following compounds or pharmaceutically acceptable salts thereof,
  • the compound of the present invention As a class of benzoxazine spirocyclic compounds with ROR ⁇ agonistic activity, the compound of the present invention has significant in vitro activity and good pharmacokinetic properties, and can be combined with PD-1 alone in the MC38 mouse colon cancer xenograft model. Combination of antibiotics has excellent anti-tumor effect.
  • pharmaceutically acceptable refers to those compounds, materials, compositions and/or dosage forms, which are suitable for use in contact with human and animal tissues within the scope of sound medical judgment , without undue toxicity, irritation, allergic reaction or other problems or complications, commensurate with a reasonable benefit/risk ratio.
  • pharmaceutically acceptable salt refers to a salt of a compound of the present invention, which is prepared from a compound having a specific substituent found in the present invention and a relatively non-toxic acid or base.
  • base addition salts can be obtained by contacting such compounds with a sufficient amount of base, either neat solution or in a suitable inert solvent.
  • Pharmaceutically acceptable base addition salts include sodium, potassium, calcium, ammonium, organic amine or magnesium salts or similar salts.
  • acid addition salts can be obtained by contacting such compounds with a sufficient amount of the acid, either neat solution or in a suitable inert solvent.
  • Examples of pharmaceutically acceptable acid addition salts include salts of inorganic acids including, for example, hydrochloric acid, hydrobromic acid, nitric acid, carbonic acid, bicarbonate, phosphoric acid, monohydrogenphosphate, dihydrogenphosphate, sulfuric acid, Hydrogen sulfate, hydriodic acid, phosphorous acid, etc.; and organic acid salts, such as acetic acid, propionic acid, isobutyric acid, maleic acid, malonic acid, benzoic acid, succinic acid, suberic acid, Fumaric acid, lactic acid, mandelic acid, phthalic acid, benzenesulfonic acid, p-toluenesulfonic acid, citric acid, tartaric acid and methanesulfonic acid and similar acids; also salts of amino acids (such as arginine, etc.) , and salts of organic acids such as glucuronic acid.
  • Certain specific compounds of the present invention contain basic and acidic functional groups and can
  • the pharmaceutically acceptable salts of the present invention can be synthesized from the parent compound containing acid groups or bases by conventional chemical methods.
  • such salts are prepared by reacting the free acid or base form of these compounds with a stoichiometric amount of the appropriate base or acid in water or an organic solvent or a mixture of both.
  • the compounds of the invention may exist in particular geometric or stereoisomeric forms.
  • the present invention contemplates all such compounds, including cis and trans isomers, (-)- and (+)-enantiomers, (R)- and (S)-enantiomers, diastereomers isomers, (D)-isomers, (L)-isomers, and their racemic and other mixtures, such as enantiomerically or diastereomerically enriched mixtures, all of which are subject to the present within the scope of the invention.
  • Additional asymmetric carbon atoms may be present in substituents such as alkyl groups. All such isomers, as well as mixtures thereof, are included within the scope of the present invention.
  • enantiomer or “optical isomer” refer to stereoisomers that are mirror images of each other.
  • cis-trans isomers or “geometric isomers” arise from the inability to rotate freely due to the double bond or the single bond of the carbon atoms forming the ring.
  • diastereoisomer refers to stereoisomers whose molecules have two or more chiral centers and which are not mirror images of the molecules.
  • keys with wedge-shaped solid lines and dotted wedge keys Indicates the absolute configuration of a stereocenter, with a straight solid-line bond and straight dashed keys Indicates the relative configuration of the stereocenter, with a wavy line Indicates wedge-shaped solid-line bond or dotted wedge key or with tilde Indicates a straight solid line key and straight dashed keys
  • tautomer or “tautomeric form” means that isomers with different functional groups are in dynamic equilibrium at room temperature and are rapidly interconvertible. If tautomerism is possible (eg, in solution), then chemical equilibrium of the tautomers can be achieved.
  • proton tautomers also called prototropic tautomers
  • prototropic tautomers include interconversions via migration of a proton, such as keto-enol isomerization and imine-ene Amine isomerization.
  • Valence isomers (valence tautomers) involve interconversions by recombination of some bonding electrons.
  • keto-enol tautomerization is the interconversion between two tautomers of pentane-2,4-dione and 4-hydroxypent-3-en-2-one.
  • the terms “enriched in an isomer”, “enriched in an isomer”, “enriched in an enantiomer” or “enantiomerically enriched” refer to one of the isomers or enantiomers
  • the content of the enantiomer is less than 100%, and the content of the isomer or enantiomer is greater than or equal to 60%, or greater than or equal to 70%, or greater than or equal to 80%, or greater than or equal to 90%, or greater than or equal to 95%, or Greater than or equal to 96%, or greater than or equal to 97%, or greater than or equal to 98%, or greater than or equal to 99%, or greater than or equal to 99.5%, or greater than or equal to 99.6%, or greater than or equal to 99.7%, or greater than or equal to 99.8%, or greater than or equal to 99.9%.
  • the terms “isomer excess” or “enantiomeric excess” refer to the difference between the relative percentages of two isomers or two enantiomers. For example, if the content of one isomer or enantiomer is 90% and the other isomer or enantiomer is 10%, then the isomer or enantiomeric excess (ee value) is 80% .
  • Optically active (R)- and (S)-isomers as well as D and L-isomers can be prepared by chiral synthesis or chiral reagents or other conventional techniques. If one enantiomer of a compound of the invention is desired, it can be prepared by asymmetric synthesis or derivatization with chiral auxiliary agents, wherein the resulting diastereomeric mixture is separated and the auxiliary group is cleaved to provide pure desired enantiomer.
  • a diastereoisomeric salt is formed with an appropriate optically active acid or base, and then a diastereomeric salt is formed by a conventional method known in the art. Diastereomeric resolution is performed and the pure enantiomers are recovered. Furthermore, the separation of enantiomers and diastereomers is usually accomplished by the use of chromatography using chiral stationary phases, optionally in combination with chemical derivatization methods (e.g. from amines to amino groups formate).
  • the compounds of the present invention may contain unnatural proportions of atomic isotopes at one or more of the atoms that constitute the compounds.
  • compounds may be labeled with radioactive isotopes such as tritium ( 3 H), iodine-125 ( 125 I) or C-14 ( 14 C).
  • radioactive isotopes such as tritium ( 3 H), iodine-125 ( 125 I) or C-14 ( 14 C).
  • heavy hydrogen can be used to replace hydrogen to form deuterated drugs.
  • the bond formed by deuterium and carbon is stronger than the bond formed by ordinary hydrogen and carbon.
  • deuterated drugs can reduce toxic side effects and increase drug stability. , enhance the efficacy, prolong the biological half-life of drugs and other advantages. All changes in isotopic composition of the compounds of the invention, whether radioactive or not, are included within the scope of the invention.
  • substituted means that any one or more hydrogen atoms on a specified atom are replaced by a substituent, which may include deuterium and hydrogen variants, as long as the valence of the specified atom is normal and the substituted compound is stable.
  • any variable eg, R
  • its definition is independent at each occurrence.
  • said group may optionally be substituted with up to two R, with independent options for each occurrence of R.
  • substituents and/or variations thereof are permissible only if such combinations result in stable compounds.
  • linking group When the number of a linking group is 0, such as -(CRR) 0 -, it means that the linking group is a single bond.
  • substituent When a substituent is vacant, it means that the substituent does not exist. For example, when X in A-X is vacant, it means that the structure is actually A. When the enumerated substituent does not indicate which atom it is connected to the substituted group, this substituent can be bonded through any atom, for example, pyridyl as a substituent can be connected to any atom on the pyridine ring. The carbon atom is attached to the group being substituted.
  • linking group listed does not indicate its linking direction
  • its linking direction is arbitrary, for example,
  • the connecting group L in the middle is -MW-, at this time -MW- can connect ring A and ring B in the same direction as the reading order from left to right to form It can also be formed by connecting loop A and loop B in the opposite direction to the reading order from left to right
  • any one or more sites of the group can be linked to other groups through chemical bonds.
  • connection method of the chemical bond is not positioned, and there is an H atom at the connectable site, when the chemical bond is connected, the number of H atoms at the site will decrease correspondingly with the number of chemical bonds connected to become the corresponding valence group.
  • the chemical bonds that the site connects with other groups can use straight solid line bonds Straight dotted key or tilde express.
  • the straight-shaped solid-line bond in -OCH3 indicates that it is connected to other groups through the oxygen atom in the group;
  • the straight dotted line bond indicates that the two ends of the nitrogen atom in the group are connected to other groups;
  • the wavy lines in indicate that the 1 and 2 carbon atoms in the phenyl group are connected to other groups;
  • the number of atoms in a ring is generally defined as the number of ring members, eg, "5-7 membered ring” means a “ring” with 5-7 atoms arranged around it.
  • C 1-3 alkyl is used to denote a straight or branched chain saturated hydrocarbon group consisting of 1 to 3 carbon atoms.
  • the C 1-3 alkyl group includes C 1-2 and C 2-3 alkyl groups, etc.; it can be monovalent (such as methyl), divalent (such as methylene) or multivalent (such as methine) .
  • Examples of C 1-3 alkyl include, but are not limited to, methyl (Me), ethyl (Et), propyl (including n - propyl and isopropyl), and the like.
  • C 1-4 alkyl is used to denote a straight or branched chain saturated hydrocarbon group consisting of 1 to 4 carbon atoms.
  • the C 1-4 alkyl group includes C 1-2 , C 1-3 and C 2-3 alkyl groups, etc.; it may be monovalent (such as methyl), divalent (such as methylene) or multivalent (such as methine).
  • Examples of C 1-4 alkyl groups include, but are not limited to, methyl (Me), ethyl (Et), propyl (including n-propyl and isopropyl), butyl (including n-butyl, isobutyl , s-butyl and t-butyl) and so on.
  • C 1-6 alkyl is used to denote a straight or branched chain saturated hydrocarbon group consisting of 1 to 6 carbon atoms.
  • the C 1-6 alkyl group includes C 1-5 , C 1-4 , C 1-3 , C 1-2 , C 2-6 , C 2-4 , C 6 and C 5 alkyl, etc.; it can be Is monovalent (such as methyl), divalent (such as methylene) or multivalent (such as methine).
  • C 1-6 alkyl groups include, but are not limited to, methyl (Me), ethyl (Et), propyl (including n-propyl and isopropyl), butyl (including n-butyl, isobutyl , s-butyl and t-butyl), pentyl (including n-pentyl, isopentyl and neopentyl), hexyl, etc.
  • C2-4alkenyl is used to denote a straight or branched chain hydrocarbon group consisting of 2 to 4 carbon atoms containing at least one carbon-carbon double bond, a carbon-carbon double bond can be located anywhere in the group.
  • the C 2-4 alkenyl includes C 2-3 , C 4 , C 3 and C 2 alkenyl, etc.; the C 2-4 alkenyl can be monovalent, divalent or multivalent. Examples of C alkenyl include, but are not limited to, ethenyl, propenyl, butenyl, butadienyl, and the like.
  • C2-3 alkenyl is used to denote a straight or branched chain hydrocarbon group consisting of 2 to 3 carbon atoms containing at least one carbon-carbon double bond, a carbon-carbon double bond It can be located at any position of the group, and the C 2-3 alkenyl includes C 3 and C 2 alkenyl; the C 2-3 alkenyl can be monovalent, divalent or multivalent. Examples of C 2-3 alkenyl include, but are not limited to, ethenyl, propenyl, and the like.
  • C 1-3 alkoxy denotes those alkyl groups containing 1 to 3 carbon atoms attached to the rest of the molecule through an oxygen atom.
  • the C 1-3 alkoxy group includes C 1-2 , C 2-3 , C 3 and C 2 alkoxy groups and the like.
  • Examples of C 1-3 alkoxy include, but are not limited to, methoxy, ethoxy, propoxy (including n-propoxy and isopropoxy), and the like.
  • C 1-3 alkylamino denotes those alkyl groups containing 1 to 3 carbon atoms attached to the rest of the molecule through an amino group.
  • the C 1-3 alkylamino group includes C 1-2 , C 3 and C 2 alkylamino groups and the like.
  • Examples of C 1-3 alkylamino include, but are not limited to, -NHCH 3 , -N(CH 3 ) 2 , -NHCH 2 CH 3 , -N(CH 3 )CH 2 CH 3 , -NHCH 2 CH 2 CH 3 , -NHCH 2 CH 2 CH 3 , -NHCH 2 (CH 3 ) 2 etc.
  • C 3-4 cycloalkyl means a saturated cyclic hydrocarbon group composed of 3 to 4 carbon atoms, which is a monocyclic ring system; it may be monovalent, divalent or multivalent.
  • Examples of C 3-4 cycloalkyl include, but are not limited to, cyclopropyl, cyclobutyl and the like.
  • a heteroatom may occupy the attachment position of the heterocycloalkyl to the rest of the molecule.
  • the 4-5 membered heterocycloalkyl group includes 4-membered and 5-membered heterocycloalkyl groups.
  • Examples of 4-5 membered heterocycloalkyl groups include, but are not limited to, azetidinyl, oxetanyl, thietanyl, pyrrolidinyl, pyrazolidinyl, imidazolidinyl, tetrahydrothiophenyl (including tetrahydrothiophen-2-yl and tetrahydrothiophen-3-yl, etc.) or tetrahydrofuranyl (including tetrahydrofuran-2-yl, etc.) and the like.
  • C n-n+m or C n -C n+m includes any specific instance of n to n+m carbons, for example C 1-12 includes C 1 , C 2 , C 3 , C 4 , C 5 , C 6 , C 7 , C 8 , C 9 , C 10 , C 11 , and C 12 , also including any range from n to n+m, for example, C 1-12 includes C 1- 3 , C 1-6 , C 1-9 , C 3-6 , C 3-9 , C 3-12 , C 6-9 , C 6-12 , and C 9-12 etc.; similarly, n to n +m means that the number of atoms on the ring is n to n+m, for example, a 3-12-membered ring includes a 3-membered ring, a 4-membered ring, a 5-membered ring, a 6-membered ring, a 7-membered ring, an 8-membere
  • leaving group refers to a functional group or atom that can be replaced by another functional group or atom through a substitution reaction (eg, a nucleophilic substitution reaction).
  • a substitution reaction eg, a nucleophilic substitution reaction
  • representative leaving groups include triflate; chlorine, bromine, iodine; sulfonate groups such as mesylate, tosylate, brosylate, tosylate esters, etc.; acyloxy groups such as acetoxy, trifluoroacetoxy, and the like.
  • protecting group includes, but is not limited to, "amino protecting group", “hydroxyl protecting group” or “mercapto protecting group”.
  • amino protecting group refers to a protecting group suitable for preventing side reactions at the amino nitrogen position.
  • Representative amino protecting groups include, but are not limited to: formyl; acyl, such as alkanoyl (such as acetyl, trichloroacetyl or trifluoroacetyl); alkoxycarbonyl, such as tert-butoxycarbonyl (Boc) ; arylmethoxycarbonyl, such as benzyloxycarbonyl (Cbz) and 9-fluorenylmethyloxycarbonyl (Fmoc); arylmethyl, such as benzyl (Bn), trityl (Tr), 1,1-di -(4'-methoxyphenyl)methyl; silyl groups such as trimethylsilyl (TMS) and tert-butyldimethylsilyl (TBS) and the like.
  • acyl such as alkanoyl (such as acetyl, trichloroacetyl or trifluoroacetyl); alkoxycarbonyl, such as
  • hydroxyl protecting group refers to a protecting group suitable for preventing side reactions of the hydroxy group.
  • Representative hydroxy protecting groups include, but are not limited to: alkyl groups such as methyl, ethyl, and tert-butyl; acyl groups such as alkanoyl (such as acetyl); arylmethyl groups such as benzyl (Bn), p-formyl Oxybenzyl (PMB), 9-fluorenylmethyl (Fm) and diphenylmethyl (diphenylmethyl, DPM); silyl groups such as trimethylsilyl (TMS) and tert-butyl Dimethylsilyl (TBS) and the like.
  • alkyl groups such as methyl, ethyl, and tert-butyl
  • acyl groups such as alkanoyl (such as acetyl)
  • arylmethyl groups such as benzyl (Bn), p-formyl Oxybenzyl (P
  • the compounds of the present invention can be prepared by a variety of synthetic methods well known to those skilled in the art, including the specific embodiments listed below, the embodiments formed by combining them with other chemical synthesis methods, and the methods well known to those skilled in the art Equivalent alternatives, preferred embodiments include but are not limited to the examples of the present invention.
  • the structure of the compounds of the present invention can be confirmed by conventional methods known to those skilled in the art. If the present invention involves the absolute configuration of the compound, the absolute configuration can be confirmed by conventional technical means in the art. For example, in single crystal X-ray diffraction (SXRD), the cultured single crystal is collected with a Bruker D8 venture diffractometer to collect diffraction intensity data, the light source is CuK ⁇ radiation, and the scanning method is: After scanning and collecting relevant data, the absolute configuration can be confirmed by further analyzing the crystal structure by direct method (Shelxs97).
  • SXRD single crystal X-ray diffraction
  • aq stands for water
  • HATU O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphonic acid Salt
  • EDC stands for N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride
  • m-CPBA stands for 3-chloroperoxybenzoic acid
  • eq stands for equivalent, equivalent
  • CDI DCM stands for dichloromethane
  • PE stands for petroleum ether
  • DIAD diisopropyl azodicarboxylate
  • DMF stands for N,N-dimethylformamide
  • DMSO stands for dimethylsulfoxide
  • EtOAc stands for acetic acid EtOH stands for ethanol
  • MeOH stands for methanol
  • CBz stands for benzyloxycarbonyl, an amine protecting group
  • compound 1-1 (2.20g, 10.6mmol) was dissolved in anhydrous methanol (20mL), potassium carbonate (2.92g, 21.1mmol) and 1-2 (2.43g, 12.7mmol) were added, and the reaction solution After stirring at 25°C for 12 hours, water (40 mL) was added to the reaction solution, and extracted with ethyl acetate (50 mL x 1). The organic phase was washed with saturated brine (50mL x 1), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the residue was separated and purified by silica gel column chromatography (50:1 petroleum ether/ethyl acetate) to obtain compound 1-3 .
  • 1 H NMR 400 MHz, CDCl 3
  • ⁇ 7.56-7.51 (m, 2H), 7.33-7.29 (m, 1H), 3.64 (s, 1H).
  • compound 1-3 (1.38g, 6.75mmol) was dissolved in anhydrous methanol (15mL), then 1-4 (2.57g, 10.1mmol), copper powder (42.9mg, 0.675mmol) and potassium carbonate were added (1.86g, 13.5mmol), the reaction solution was stirred at 25°C for 12 hours, the reaction solution was spin-dried, added ethyl acetate (50mL), filtered, the filter cake was washed with ethyl acetate (10mL), and the filtrate was concentrated under reduced pressure , the residue was separated and purified by silica gel column chromatography (20:1 petroleum ether/ethyl acetate) to obtain compound 1-5.
  • diboronic acid pinacol ester (819mg, 3.23mmol) was added into anhydrous tetrahydrofuran (10mL), then cuprous chloride (29.0mg, 0.293mmol) and 4,5-bis(diphenylphosphine) were added -9,9-Dimethylxanthene (170mg, 0.293mmol), the reaction solution was stirred at 25°C for 5 minutes, then sodium tert-butoxide (310mg, 3.23mmol) was added, and the reaction solution was stirred at 25°C for 5 minutes , then added compound 1-3 (600mg, 2.93mmol) and iodomethane (1.67g, 11.7mmol), the reaction solution was stirred at 25°C for 710 minutes, water (20mL) was added to the reaction solution, and ethyl acetate (20mL x 1) extraction, the organic phase was washed with saturated brine (20mLx 1), dried over anhydrous sodium sulf
  • Zinc dust (1.81 g, 27.7 mmol) and 1,2-dibromoethane (307 mg, 1.63 mmol) were added to N,N-dimethylformamide (20 mL).
  • the reaction solution was stirred and reacted at 70° C. for 10 minutes.
  • the reaction solution was then cooled to 20°C.
  • Chlorotrimethylsilane (177mg, 1.63mmol) was added dropwise to the reaction solution, and then the reaction solution was stirred at 20°C for 50 minutes.
  • reaction solution was filtered through diatomaceous earth, the filter residue was washed with ethyl acetate (30mL), the filtrate was washed with saturated ammonium chloride aqueous solution (30mL ⁇ 1), and the organic phase was sequentially washed with water (30mL ⁇ 3) and saturated brine (30mL ⁇ 1). After washing, drying with anhydrous sodium sulfate, filtration, the filtrate was concentrated under reduced pressure, and the residue was separated and purified by silica gel column chromatography (4/1 petroleum ether/ethyl acetate) to obtain compound 15-3.
  • ROR ⁇ ligand-binding domain LBD
  • TR-FRET time-resolved fluorescence energy transfer
  • the compound to be tested was diluted in DMSO and further diluted in assay buffer (50mM Tris pH 7.0, 50mM KCl, 1mM Na-EDTA, 0.1mM DTT, 0.01% BSA) (4-fold dilution, 10 concentrations, highest concentration 5000 nM), the final DMSO concentration was 1%.
  • the hROR ⁇ -LBD protein was diluted in assay buffer to give a final hROR ⁇ -LBD concentration of 15 nM in 384-well plates.
  • a stock solution of biotin-SRC1 polypeptide Biotin-SPSSHSSSLTERHKILHRLLQEGSP was prepared in assay buffer and added to each well (final concentration 200 nM). Solutions of SA-eu (1 nM final concentration) and SA-APC (50 nM final concentration) were also added to each well.
  • the final assay mixture was incubated overnight at 4°C, equilibrated at room temperature for 1 hour, and centrifuged at 1000 rpm for 1 minute. Fluorescence readings were detected on the Envision microplate detector, and the logarithmic curve of the ratio of the fluorescence signal at emission wavelength 665nM/615nM to the compound concentration was drawn by GraphPad Prism software, and the 50% effective concentration (EC 50 ) of the compound was calculated. The maximum response (E max ) was the upper peak peak of the signal determined by GraphPad Prism fit.
  • Mouse CD4+T cell isolation kit (Mouse CD4+T cell isolation kit) (Stemcell)
  • Non-essential amino acids (Gibco)
  • the CD3 antibody was diluted to 5 ⁇ g/mL in DPBS, added to a 96-well U-bottom plate, 50 ⁇ L of liquid per well, and coated overnight at 4°C.
  • C57BL/6 mouse spleen in culture medium RPMI 1640 + 10% fetal bovine serum + 1% penicillin + 1% non-essential amino acid + 0.05mM ⁇ -mercaptoethanol
  • RPMI 1640 + 10% fetal bovine serum + 1% penicillin + 1% non-essential amino acid + 0.05mM ⁇ -mercaptoethanol pass through a 70 ⁇ m filter to prepare a single cell suspension , centrifuge at 300g for 3min. Add erythrocyte lysate to lyse at room temperature for 3 min.
  • CD4 + cells were isolated using the mouse CD4 + T cell isolation kit.
  • CD4 + cells obtained above at a density of 5*10 5 /mL into the coated wells , 200 ⁇ L cell suspension per well; then add CD28 antibody (3 ⁇ g/mL), TGF ⁇ (3ng/mL), IL-6 (30ng/mL), IL-23 (10ng/mL), IL-1 ⁇ (10ng/mL ), IFN ⁇ antibody (10 ⁇ g/mL) and IL-4 antibody (10 ⁇ g/mL); then the compound of the present invention was added to the well, and cultured at 37° C. under 5% CO 2 for 3 days.
  • the U-bottom plate was centrifuged at 300 g for 3 min, the supernatant was discarded, and washed twice with staining buffer.
  • the IL-17A antibody was diluted 1:200 in permeabilization buffer, 50 ⁇ L of dye solution was added to each well, stained at room temperature for 30 min, and then washed twice with staining buffer. Finally, the cells were resuspended with 150 ⁇ L staining buffer, and the proportion of Th17 cells was detected by flow cytometry.
  • Compound test concentration 1 ⁇ M.
  • the compounds of the present invention can obviously promote the differentiation of CD4 + cells into Th17 cells.
  • the pharmacokinetic characteristics of the compounds were tested in rodents after intravenous injection and oral administration according to the standard protocol.
  • the mice were given a single intravenous injection (IV) and oral administration (PO).
  • the solvent for intravenous injection is a mixed solvent made up of 5% dimethyl sulfoxide, 30% PEG400, and 65% 10% hydroxypropyl ⁇ -cyclodextrin.
  • the oral vehicle is a mixed vehicle made of 0.5% hypromellose and 0.2% Tween.
  • the project used four female Balb/c mice, two mice were administered intravenously, the dose was 0.5mg/kg, and the collection 0h (before administration) and after administration were 0.0833, 0.25, 0.5, 1, Plasma samples at 2, 4, 8, and 24 hours were administered orally to the other two mice at a dose of 1 mg/kg, collected at 0 h (before administration) and at 0.25, 0.5, 1, 2, and 4 hours after administration , 8, 24h plasma samples, collect whole blood samples within 24 hours, centrifuge at 3000g for 15 minutes, separate supernatant to obtain plasma samples, add 4 times volume of acetonitrile solution containing internal standard to precipitate protein, centrifuge to take supernatant and add equal volume The water was then centrifuged to take the supernatant sample, and the blood drug concentration was quantitatively analyzed by LC-MS/MS analysis method, and the pharmacokinetic parameters were calculated, such as peak concentration (C max ), clearance rate (CL), half-life (T 1 / 2 ), tissue distribution (V
  • the compounds of this invention have good pharmacokinetic properties, including good oral bioavailability, oral exposure, half-life and clearance rate.
  • the purpose of this experiment is to study the evaluation of the compound of the present invention on the MC38 mouse colon cancer xenograft tumor model in vivo.
  • the culture medium is 1640 medium containing 10% fetal bovine serum, and the culture condition is 37°C, 5% carbon dioxide.
  • the subculture ratio was 1:2 ⁇ 1:3, and subcultured 2 ⁇ 3 times a week.
  • 0.1 mL (2 ⁇ 10 5 ) cells were inoculated subcutaneously on the right back of each mouse. On the same day, animals were randomized into groups based on body weight.
  • the experimental vehicle was 5% DMSO/95% (20% hydroxypropyl beta cyclodextrin).
  • the test substance was dissolved in a solvent, prepared into a uniform solution with a certain concentration, and stored at 4°C.
  • the experimental index is to investigate whether tumor growth is inhibited, delayed or cured.
  • Tumor diameters were measured twice a week with vernier calipers.
  • T/C Relative tumor proliferation rate
  • RTV relative tumor volume
  • PD-1 monoclonal antibody BioXcell. PD-1 monoclonal antibody was administered on the 7th day after grouping, and compound 1 was administered on the day of grouping.
  • the combination of the compound of the present invention and PD-1 monoclonal antibody has an excellent tumor-inhibiting effect on the transplanted tumor model of MC38 mouse colon cancer.

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Abstract

L'invention concerne une classe de composés spiro de benzoxazine et un procédé de préparation correspondant, et l'utilisation de cette classe de composés dans la préparation d'un médicament pour le traitement de maladies associées. De façon spécifique, l'invention concerne un composé représenté par la formule (I) et un sel pharmaceutiquement acceptable de celui-ci.
PCT/CN2022/111883 2021-08-13 2022-08-11 Classe de composés spiro de benzoxazine et procédé de préparation correspondant Ceased WO2023016527A1 (fr)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023232870A1 (fr) 2022-05-31 2023-12-07 Immunic Ag Modulateurs de rorg/rorgt pour le traitement d'infections virales de type covid-19

Citations (4)

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Publication number Priority date Publication date Assignee Title
WO2015171610A2 (fr) * 2014-05-05 2015-11-12 Lycera Corporation Sulfonamide de tétrahydroquinoline et composés apparentés destinés à servir d'agonistes de rory et pour le traitement de maladies
WO2016179343A1 (fr) * 2015-05-05 2016-11-10 Lycera Corporation Sulfonamides de dihydro-2h-benzo[b][1,4]oxazine et composés apparentés destinés à être utilisés comme agonistes de rorγ et pour le traitement de maladies
CN106132422A (zh) * 2014-02-27 2016-11-16 莱斯拉公司 使用视黄酸受体相关孤儿受体γ的激动剂的过继细胞疗法＆相关治疗方法
CN109568321A (zh) * 2019-01-14 2019-04-05 山东轩竹医药科技有限公司 RORγ调节剂

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106132422A (zh) * 2014-02-27 2016-11-16 莱斯拉公司 使用视黄酸受体相关孤儿受体γ的激动剂的过继细胞疗法＆相关治疗方法
WO2015171610A2 (fr) * 2014-05-05 2015-11-12 Lycera Corporation Sulfonamide de tétrahydroquinoline et composés apparentés destinés à servir d'agonistes de rory et pour le traitement de maladies
WO2016179343A1 (fr) * 2015-05-05 2016-11-10 Lycera Corporation Sulfonamides de dihydro-2h-benzo[b][1,4]oxazine et composés apparentés destinés à être utilisés comme agonistes de rorγ et pour le traitement de maladies
CN109568321A (zh) * 2019-01-14 2019-04-05 山东轩竹医药科技有限公司 RORγ调节剂

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023232870A1 (fr) 2022-05-31 2023-12-07 Immunic Ag Modulateurs de rorg/rorgt pour le traitement d'infections virales de type covid-19

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