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NZ713458B2 - 6,7-DIHYDROPYRAZOLO[1,5-a]PYRAZIN-4(5H)-ONE COMPOUNDS AND THEIR USE AS NEGATIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS - Google Patents

6,7-DIHYDROPYRAZOLO[1,5-a]PYRAZIN-4(5H)-ONE COMPOUNDS AND THEIR USE AS NEGATIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS Download PDF

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Publication number
NZ713458B2
NZ713458B2 NZ713458A NZ71345814A NZ713458B2 NZ 713458 B2 NZ713458 B2 NZ 713458B2 NZ 713458 A NZ713458 A NZ 713458A NZ 71345814 A NZ71345814 A NZ 71345814A NZ 713458 B2 NZ713458 B2 NZ 713458B2
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New Zealand
Prior art keywords
4alkyl
pyrazin
dihydropyrazolo
compound
disorders
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NZ713458A
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NZ713458A (en
Inventor
De Diego Sergio Alvar Alonso
Gil Jose Ignacio Andres
Nunez Jose Maria Cid
Annelies Marie Antonius Decorte
Gonzalez Oscar Delgado
Molina Aranzazu Garcia
Gregor James Macdonald
Antonius Adrianus Hendrikus Petrus Megens
Suarez Andres Avelino Trabanco
Gool Michiel Luc Maria Van
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Janssen Pharmaceutica Nv
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Priority claimed from PCT/EP2014/061478 external-priority patent/WO2014195311A1/en
Publication of NZ713458A publication Critical patent/NZ713458A/en
Publication of NZ713458B2 publication Critical patent/NZ713458B2/en

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/20—Hypnotics; Sedatives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07—Optical isomers
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems

Abstract

The present invention relates to novel 6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one derivatives of Formula (I) as negative allosteric modulators (NAMs) of the metabotropic glutamate receptor subtype 2 ("mGluR2"). The invention is also directed to pharmaceutical compositions comprising such compounds, to processes for preparing such compounds and compositions, and to the use of such compounds and compositions for the prevention or treatment of disorders in which the mGluR2 subtype of metabotropic receptors is involved, especially CNS disorders. to processes for preparing such compounds and compositions, and to the use of such compounds and compositions for the prevention or treatment of disorders in which the mGluR2 subtype of metabotropic receptors is involved, especially CNS disorders.

Description

,7—DIHYDROPYRAZOLO[1,5-a]PYRAZIN-4(SIfl-ONE NDS AND THEIR USE AS NEGATIVE ALLOSTERIC MODULATORS OF MGLURZ RECEPTORS Field of the Invention The present invention relates to novel 6,7-dihydropyrazolo[l yrazin-4(5H)-one derivatives as negative allosteric modulators (NAMs) of the metabotropic glutamate receptor subtype 2 ("mGluR2"). The invention is also directed to pharmaceutical compositions comprising such compounds, to processes for preparing such compounds and compositions, and to the use of such compounds and compositions for the prevention or treatment of disorders in which the mGluR2 e of metabotropic receptors is ed.
Background of the Invention The glutamatergic system in the CNS is one of the neurotransmitter systems that play a key role in several brain fianctions. Metabotropic glutamate receptors (mGluR) belong to the G-protein-coupled family, and eight different subtypes have been identified to date, which are buted to various brain regions (Ferraguti & Shigemoto, Cell & Tissue Research, 326:483-504, 2006). mGluRs participate in the modulation of ic transmission and neuronal excitability in the CNS by the binding of glutamate.
This tes the receptor to engage intracellular signaling partners, leading to ar events (Niswender & Conn, Annual Review of Pharmacology & Toxicology 50:295- 322, 20 l 0). mGluRs are further d into three subgroups based on their pharmacological and structural properties: group-I (mGluRl and mGluRS), group-ll (mGluR2 and mGluR3) and group-III (mGluR4, mGluR6, mGluR7 and mGluR8). Group-ll ligands, both orthosteric and allosteric modulating, are considered to be potentially useful in the treatment of various neurological disorders, including psychosis, mood ers, Alzheimer e and cognitive or memory deficiencies. This is tent with their primary localisation in brain areas such as the cortex, hippocampus and the striatum (Ferraguti & Shigemoto, Cell & Tissue Research 326:483-504, 2006). Particularly antagonists and negative allosteric tors are reported to hold potential for the treatment of mood disorders and cognitive or memory dysfunction. This is based on findings with ll receptor nists and negative allosteric modulators tested in laboratory animals subjected to a range of experimental conditions deemed relevant to these clinical syndromes (Goeldner et al, Neuropharmacology 64:337-346, 2013). al trials are, for example, underway with mGluR2/3 antagonist RO4995819 (F. Hoffmann-La Roche Ltd.) in adjunctive therapy in patients with Major Depressive Disorder having inadequate response to ongoing antidepressant treatment (ClinicalTrials.gov Identifier NCT01457677, retrieved 19 February 2014).
WO 2013066736 (Merck Sharp & Dohme Corp.) describes quinoline carboxamide and quinoline itrile compounds as mGluR2 NAMs. WO2013174822 n therapeutics) describes 4H-pyrazolo[1,5-a]quinazolinones and 4H-pyrrolo[1,2- a] quinazolin-S -ones and in Vitro mGluR2 NAM actiVity thereof. WO 4028 (F. Hoffman-La Roche AG) discloses a selection of mGlu2/3 ve allosteric modulators and their potential use in the treatment of Autistic Spectrum Disorders (ASD).
The II receptors are mainly d on presynaptic nerve terminals where they exert a ve feedback loop to the release of glutamate into the synapse (Kelmendi et al, Primary Psychiatry 13 :80-86, 2006). Functional inhibition of these receptors by nists or negative allosteric modulators therefore lifts the brake on glutamate release, resulting in enhanced glutamatergic signaling. This effect is believed to underlie the antidepressant-like and procognitive effects observed in preclinical species with inhibitors of the Group-II receptor. In addition, treatment of mice with group-II teric antagonists has been shown to enhance signaling by grth factors such as brain derived neurotrophic factor (BDNF) (Koike et al, Behavioural Brain Research 238:48-52, 2013). Since BDNF and other growth factors have been shown to be critically involved mediating synaptic plasticity, this mechanism is likely to contribute to both antidepressant and procognitive properties of these nds. Inhibition of mGluRs of the group-II receptor family is therefore considered to represent a potential eutic mechanism for neurological ers, including depression and cognitive or memory dysfunction. ption of the Invention The present invention is directed to 6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one derivatives of Formula (I) 0 R2 R\NM 3 4 R R (1) and stereoisomeric forms thereof, WO 95311 2014/061478 wherein R1 is phenyl or 2-pyridinyl, each optionally substituted with one or more substituents each independently selected from the group of halo, C1_4alkyl, mono- or aloC1_4alkyl, -O-C1_4alkyl, -C1_4alkyl-O-C1_4alkyl, mono- or poly-haloC1_4alkyloxy, -C1_4alkyl-OH, C1_4alkylthio, mono- or poly-haloC1_4alkylthio, cyano, cloalkyl optionally substituted with trifluoromethyl, and —SF5; or is "CE? R2 is selected from R6 R5 i and : wherein R5 and R6 are each independently selected from the group of hydrogen, halo, cyano, C1_4alkyl, -C1_4alkyl-OH, C3_7cycloalkyl, mono- or poly-haloC1_4alkyl, -C1_4alkyl-O-C1_4alkyl, -O-C1_4alkyl, mono- or poly-haloC1_4alkyloxy, l-acetylazetidin- 3-yl, and NR’R"; wherein R’ is selected from hydrogen and C1_4alkyl; R" is selected from hydrogen and kyl; or R’ and R" together with the Nitrogen atom to which they are attached form a heterocyclic group selected from the group of l-azetidinyl, l-pyrrolidinyl, l-piperidinyl, razinyl, and 4-morpholinyl; wherein each of the heterocyclic groups may be optionally substituted with a substituent ed from halo, hydroxyl, C1_4alkyl, mono- or poly-haloC1_4alkyl, and —(CO)C1_4alkyl; R3 is selected from hydrogen and C1_4alkyl; R4 is selected from the group of hydrogen, C1_4alkyl, mono- or poly-haloC1_4alkyl, -C1_4alkyl-O-C1_4alkyl, and -C1_4alkyl-OH; and the N—oxides, and the pharmaceutically acceptable salts and the solvates thereof.
The present invention also relates to a pharmaceutical composition comprising a therapeutically effective amount of a compound of Formula (I) and a pharmaceutically acceptable r or excipient.
Additionally, the invention relates to a compound of a (I) for use as a medicament, and to a compound of Formula (I) for use in the treatment or in the prevention of central nervous system conditions or diseases selected from mood disorders; delirium, ia, amnestic and other cognitive disorders; disorders usually first diagnosed in infancy, childhood or adolescence; nce-related disorders; schizophrenia and other psychotic disorders; somatoform disorders; and hypersomnic sleep disorder.
The invention also relates to the use of a compound of Formula (I) in combination with an additional ceutical agent for use in the treatment or prevention of l nervous system conditions or diseases selected from mood disorders; delirium, dementia, amnestic and other cognitive disorders; disorders usually first diagnosed in infancy, childhood or adolescence; substance-related disorders; schizophrenia and other psychotic disorders; somatoform disorders; and hypersomnic sleep disorder.
Furthermore, the invention relates to a process for preparing a pharmaceutical composition according to the invention, terized in that a pharmaceutically acceptable carrier is intimately mixed with a therapeutically effective amount of a compound of Formula (I).
The invention also relates to a method of treating or ting a central s system disorder selected from mood disorders; delirium, dementia, amnestic and other cognitive disorders; ers usually first diagnosed in infancy, childhood or adolescence; substance-related ers; schizophrenia and other psychotic ers; somatoform disorders; and hypersomnic sleep disorder comprising administering to a subject in need thereof, a therapeutically effective amount of a compound of Formula (I) or a therapeutically effective amount of a pharmaceutical composition according to the invention.
The ion also relates to a t comprising a compound of Formula (I) and an additional pharmaceutical agent, as a combined preparation for aneous, separate or sequential use in the treatment or prevention of central nervous system conditions or diseases selected from mood disorders; delirium, dementia, amnestic and other cognitive disorders; disorders usually first diagnosed in infancy, childhood or adolescence; nce-related disorders; phrenia and other tic disorders; somatoform disorders; and hypersomnic sleep disorder.
Description of the figures Figure 1 shows the frequency distributions for distance travelled obtained in ical series of t-pretreated control rats. In figure 1, — corresponds to scopolamine + JNJ 42153605; - - - corresponds to amine alone; and — — — corresponds to no challenge.
Figure 2 shows the effect of Co. No. 1 (mg/kg p.0., 4 h prior to test) on ation times of the new vs. the familiar arm by rats in the e or presence of PCP (0 (= veh) or 0.75 mg/kg s.c., 0.5 h prior to test) in the V-maze. Data are reported as Mean :: SEM, n = lZ/group; ANOVA with LSD-post hoc, p vs. familiar arm: *** p<0.001, *<0.05.
Figure 3 shows the interaction of Co. No. l with reserpine in rats.
Shown are the s on pupil diameter before reserpine challenge (Fig. 3a) and the reversal of the reserpine-induced ptosis (Fig. 3b), miosis (Fig. 3c) and sedation (Fig. 3d) measured 1 h after so. (left panel), 1 h after p.o. (middle panel) and 4 h after p.o. (right panel) administration of Co. No. 1.
Figure 4 rates the placement of the hippocampus brain slice in a well of a MBA biochip, with 60 X 3D-tip electrodes (black dots). Traces show the recorded potential at each electrode (Fig. 4a), and the captured fEPSP traces of paired pulses separated by 30 ms (Fig. 4b). The preparation was ed with artificial cerebrospinal fluid (ACSF). (3D = three-dimensional; fEPSP = field excitatory postsynaptic potentials; MEA = micro-electrode array; ms = milliseconds).
Figure 5 shows how Co. No. l restores fEPSP depressed by 1 uM LY-354740 in the dentate gyrus of rat hippocampal brain slices.
Figure 5a: fEPSP ude (% of baseline) is shown after the application of LY-354740 (1 uM), followed by the application of Co. No. l (10 uM), and then by the application of the mGlu2 antagonist LY-34l495, and finally by a washout. At the end of experiments, the AMPA antagonist CNQX (6-cyanonitroquinoxaline-2,3-dione, 50 uM) and kynurenic acid (1 mM) were added as controls to block glutamate-mediated fEPSP.
Figure 5b: The same experiments as shown in Figure 5a, but presenting the PPR results. The error bars represent the SEM of 17 independent slices from 4 SD rats.
(ACSF = artificial cerebrospinal fluid; fEPSP = field excitatory postsynaptic potential; PPR = paired-pulse ratio; SEM = standard error of the mean).
Figure 6 shows how Co. No. l facilitates long-term potentiation in the dentate gyrus of rat hippocampal brain slices.
Monitoring of the post-synaptic response for 80 min shows induction of LTP after weak theta stimulation (at 30 min).
Figure 6a: fEPSP in response to the weak theta stimulus under control conditions (vehicle: open s) and following the application of 10 uM Co. No. 1 (solid circles).
Figure 6b: FTP and LTP under control conditions and after application of 10 uM Co.
No. l. The error bars represent the SEM of 22 independent slices from 4 SD rats.
LTP = long-term potentiation; NAM = negative allosteric modulator; PTP = heta potentiation; SEM = standard error of the mean. ed description of the invention The present ion s in particular to compounds of Formula (I) as defined hereinabove, and stereoisomeric forms thereof, wherein R1 is phenyl or 2-pyridinyl, each optionally substituted with one or more substituents each independently selected from the group of halo, C1_4alkyl, mono- or poly-haloC1_4alkyl, -O-C1_4alkyl, -C1_4alkyl-O-C1_4alkyl, mono- or poly-haloC1_4alkyloxy, -C1_4alkyl-OH, mono- or poly-haloC1_4alkylthio, cyano, and —SF5;oris __I_CEO] R2 is selected from R5 N\ R6 R5 U \ N i and : wherein R5 and R6 are each ndently selected from the group of hydrogen, halo, cyano, C1_4alkyl, -C1_4alkyl-OH, cloalkyl, mono- or poly-haloC1_4alkyl, -C1_4alkyl-O-C1_4alkyl, -O-C1_4alkyl, mono- or poly-haloC1_4alkyloxy, and NR’R"; wherein R’ is selected from hydrogen and C1_4alkyl; R" is selected from hydrogen and C1_4alkyl; or R’ and R" together with the Nitrogen atom to which they are attached form a heterocyclic group selected from the group of idinyl, l-pyrrolidinyl, and l-piperidinyl; wherein each of the heterocyclic groups may be optionally tuted with a halo substituent; R3 is selected from hydrogen and C1_4alkyl; R4 is selected from the group of hydrogen, kyl, mono- or poly-haloC1_4alkyl, -C1_4alkyl-O-C1_4alkyl, and -C1_4alkyl-OH; and the N—oxides, and the pharmaceutically acceptable salts and the solvates thereof.
In an additional embodiment, the present invention relates to compounds of Formula (I) as defined hereinabove, and stereoisomeric forms f, wherein R1 is phenyl ally substituted with one, two or three substituents each independently selected from the group of halo, C1_4alkyl, mono- or poly-haloC1_4alkyl, -O-C1_4alkyl, -C1_4alkyl-O-C1_4alkyl, mono- or aloC1_4alkyloxy, mono- or polyhaloC1 _4alkylthio, cyano, and —SF5; or 2-pyridinyl optionally tuted with one or two substituents each independently selected from the group of halo, C1_4alkyl, mono- or poly-haloC1_4alkyl, and -O-C1_4alkyl; R2 is wherein R5 and R6 are each independently selected from the group of hydrogen, halo, cyano, kyl, C3_7cycloalkyl, mono- or poly-haloC1_4alkyl, -O-C1_4alkyl, mono- or poly-haloC1_4alkyloxy, and NR’R"; wherein R’ is selected from hydrogen and C1_4alkyl; R" is ed from hydrogen and C1_4alkyl; or R’ and R" together with the Nitrogen atom to which they are attached form a heterocyclic group ed from the group of l-azetidinyl, 1-pyrrolidinyl, and l-piperidinyl; wherein each of the heterocyclic groups may be optionally substituted with a halo substituent; R3 is selected from hydrogen and C1_4alkyl; R4 is selected from the group of C1_4alkyl, mono- or poly-haloC1_4alkyl, and -C1_4alkyl-O-C1_4alkyl; in particular >CR3R4 is selected from the group of >CH(CH3), >CH(CH2CH3), 2F), and >CH(CH20CH3); and the es, and the pharmaceutically acceptable salts and the solvates thereof.
In an additional embodiment, the present invention relates to compounds of Formula (I) as defined hereinabove, and stereoisomeric forms thereof, wherein R1 is phenyl optionally substituted with one, two or three tuents each independently selected from the group of halo, C1_4alkyl, poly-haloC1_4alkyl, -O-C1_4alkyl, -C1_4alkyl-O-C1_4alkyl, poly-haloC1_4alkyloxy, poly-haloC1_4alkylthio, cyano, and —SF5; or 2-pyridinyl optionally substituted with one or two substituents each independently ed from the group of halo, C1_4alkyl, mono- or poly-haloC1_4alkyl, and 4alkyl; R2 is wherein R5 and R6 are each independently selected from the group of hydrogen, cyano, C1_4alkyl, poly-haloC1_4alkyl, -O-C1_4alkyl, and NR’R"; wherein R’ is selected from hydrogen and C1_4alkyl; R" is C1_4alkyl; or R’ and R" together with the Nitrogen atom to which they are ed form a l -azetidinyl; R3 is selected from hydrogen and C1_4alkyl; R4 is ed from the group of C1_4alkyl, mono- or poly-haloC1_4alkyl, and -C1_4alkyl-O-C1_4alkyl; in particular >CR3R4 is selected from the group of >CH(CH3), >CH(CH2CH3), >CH(CH2F), and >CH(CH20CH3); and the N—oxides, and the pharmaceutically acceptable salts and the es thereof.
In an additional embodiment, the present invention relates to compounds of Formula (I) as defined hereinabove, and stereoisomeric forms thereof, wherein R1 is selected from (a) a substituted phenyl selected from the group of F3C\© F3CO\© C|\© F CI F5S\© Fgci i F30, i CN \0 F30 F30, i F30, i 9 ‘ o Q oJ' F3C Q Q I g9. ~ ; or (b) a substituted 2-pyridinyl ed from the group of /\o /\o F3C \ N | F3C\© c | \ | 9 / \\ ;and / \\ R2 is selected from the group of I \N / I \N 9 / ; x / .
CFs \O \NH \N \N \N I | | / / , / . m <9 \ \ I /N I /N \N 9 9 x" / .
CN \NH R3 is selected from hydrogen and C1_4alkyl; R4 is selected from the group of C1_4alkyl, mono- or poly-haloC1_4alkyl, and -C1_4alkyl-O-C1_4alkyl; in particular >CR3R4 is selected from the group of >CH(CH3), >CH(CH2CH3), 2F), and >CH(CH20CH3); and the es, and the pharmaceutically acceptable salts and the solvates thereof.
In an additional embodiment, the present invention relates to compounds selected from the group of (7S)Methyl(2-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo [l ,5 -a]pyrazin-4(5H)-one; (7S)[3-Ethoxy(trifluoromethyl)phenyl]methyl-3 -(2-methylpyridinyl)-6,7- dihydropyrazolo [l ,5 -a]pyrazin-4(5H)-one; _ 10 _ (7S)(4-Ch10r0pheny1)—7-methy1-3 -(2-rnethy1pyridiny1)-6,7-dihydr0pyrazolo [1 ,5 - a]pyrazin-4(5H)-one; (7S)-5 -[3 -Meth0xy(trifluor0rnethy1)pheny1]rnethy1-3 -(2-rnethy1pyridiny1)- 6 5 -a]pyrazin-4(5H)-one; , 7-dihydr0pyraz010 [1 , (7S)Methy1pyridiny1-5 -[4-(trifluoromethy1)pheny1]-6,7-dihydr0pyraz010[1 ,5 - zin-4(5H)-one; (7S)Methy1-3 -(2-rnethy1pyridiny1)-5 - [5 -(trifluor0rnethy1)pyridiny1] -6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 ,4-Dich10r0pheny1)—7-methy1-3 -(2-methy1pyridiny1)-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -[6-Eth0xy-5 -(trifluor0rnethy1)pyridiny1] rnethy1-3 -(2-rnethy1pyridiny1)- 6 5 -a]pyrazin-4(5H)-one; , dr0pyraz010 [1 , (7S)Methy1-3 -(2-rnethy1pyridiny1)-5 - [4-(pentafluoro-k6-su1fany1)pheny1]-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methy1-3 -(2-rnethy1pyridiny1)-5 - [3 -rnethy1(trifluoromethy1)pheny1]-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-3 -(2,6-Dirnethy1pyridiny1)rnethy1-5 rifluoromethy1)pheny1]-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -[3 -Ch10ro(trifluor0rnethy1)pheny1]rnethy1-3 -(2-methy1pyridiny1)—6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -[3 -F1u0ro(triflu0romethy1)pheny1]rnethy1-3 -(2-rnethy1pyridiny1)-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -[4-Ch10r0-3 -(trifluorornethy1)pheny1]rnethy1-3 -(2-methy1pyridiny1)—6,7- opyrazolo [1 ,5 -a]pyrazin-4(5H)-one; - [(7S)Methy1-3 -(2-rnethy1pyridiny1)0X0-6,7-dihydr0pyraz010[1,5 -a]pyrazin- (4H)-y1] (trifluoromethy1)benzonitrile; (7S)-3 -(2-Methoxypyridiny1)—7-methy1-5 - [4-(triflu0romethy1)pheny1]-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-3 -(2-Ethy1pyridiny1)rnethy1-5 -[4-(trifluoromethy1)pheny1]-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -[3 -Ch10r0(triflu0rornethy1)pheny1]-3 -(2 ,6-dirnethy1pyridiny1)rnethy1- 6 5 -a]pyrazin-4(5H)-one; , 7-dihydr0pyraz010 [1 , (7S)-5 -(3 ,4-Dich10r0pheny1)—3 -(2,6-dimethy1pyridiny1)rnethy1-6,7- opyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-3 thy1arnino)pyridiny1]rnethy1-5 -[4-(trifluoromethy1)pheny1]-6 ,7- opyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methy1-3 -(2-rnethy1pyridiny1)-5 - [4-(triflu0r0methoxy)pheny1]-6,7- _ 11 _ dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)[2-(Dimethylamino)pyridinyl]methyl[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)(5-Chloroethoxypyridinyl)—7-methyl(2-methylpyridinyl)-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl[2-(methylamino)pyridinyl][4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)(3,4-Dichlorophenyl)(2-methoxypyridinyl)methyl-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(2-methylpyridinyl)-5 - {4-[(trifluoromethyl)sulfanyl]phenyl} -6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; 4- {(7S)Methyloxo[4-(trifluoromethyl)phenyl]-4,5 ,6,7- tetrahydropyrazolo [1 ,5 -a]pyrazin-3 -yl}pyridinecarbonitrile; (7S)[3-Chloro(trifluoromethyl)phenyl](2-methoxypyridinyl)—7-methyl-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)[3-Chloro(trifluoromethyl)phenyl]methyl[2-(methylamino)pyridin yl]-6,7-dihydropyrazolo[1 ,5-a]pyrazin-4(5H)—one; (7S)-3 -(2-Azetidinylpyridinyl)—7-methyl-5 - [4-(trifluoromethyl)phenyl] -6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl[4-(trifluoromethyl)phenyl][2-(trifluoromethyl)pyridinyl]-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; 4- {(7S)-5 - [3 -Chloro(trifluoromethyl)phenyl] methyloxo-4,5 ,6,7- tetrahydropyrazolo [1 ,5 -a]pyrazin-3 -yl} (methylamino)pyridinecarbonitrile; (7S)(2-Methoxypyridinyl)—5-[3-methoxy(trifluoromethyl)phenyl]methyl- hydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)[3-Fluoro(trifluoromethyl)phenyl]methyl[2-(methylamino)pyridin yl]-6,7-dihydropyrazolo[1 ,5-a]pyrazin-4(5H)—one; and -Methyl(2-methylpyridinyl)[5 -(trifluoromethyl)pyridinyl]-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; and the N—oxides, and the pharmaceutically acceptable salts and the solvates thereof.
In an additional embodiment, the present invention relates to nds selected from the group of -Methyl(2-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[l,5-a]pyrazin-4(5H)-one, or a hloride salt, or a sulfate salt, or a methanesulfonate salt, or a maleate salt thereof; -[3-Ethoxy(trifluoromethyl)phenyl]methyl-3 -(2-methylpyridinyl)-6,7- _ 12 _ opyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)(4-Chlorophenyl)—7-rnethyl(2-rnethylpyridinyl)-6,7-dihydropyrazolo [1 ,5 - a]pyrazin-4(5H)-one or a hloride salt thereof; (7S)[3-Methoxy(trifluorornethyl)phenyl]rnethyl(2-rnethylpyridinyl)-6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-one or a hydrochloride salt thereof; -Methylpyridinyl-5 -[4-(trifluorornethyl)phenyl]-6,7-dihydropyrazolo[ 1 ,5 - a]pyrazin-4(5H)-one; (7S)Methyl(2-rnethylpyridinyl)[5 -(trifluorornethyl)pyridinyl]-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)(3,4-Dichlorophenyl)—7-rnethyl(2-rnethylpyridinyl)-6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-one or a hydrochloride salt thereof; (7S)[6-Ethoxy(trifluorornethyl)pyridinyl]rnethyl(2-rnethylpyridinyl)— 6,7-dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(2-rnethylpyridinyl)[4-(pentafluoro- k6-sulfanyl)phenyl]-6,7- dihydropyrazolo [1 ,5 azin-4(5H)-one; (7S)Methyl(2-rnethylpyridinyl)[3 -rnethyl(trifluorornethyl)phenyl]-6,7- opyrazolo[1,5-a]pyrazin-4(5H)-one or a hydrochloride salt thereof; (7S)(2,6-Dirnethylpyridinyl)methyl[4-(trifluorornethyl)phenyl]-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)[3-Chloro(trifluorornethyl)phenyl]rnethyl(2-rnethylpyridinyl)—6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)[3-Fluoro(trifluorornethyl)phenyl]rnethyl(2-rnethylpyridinyl)-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)[4-Chloro(trifluorornethyl)phenyl]rnethyl(2-rnethylpyridinyl)—6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; - [(7S)Methyl-3 -(2-rnethylpyridinyl)oxo-6,7-dihydropyrazolo[1,5 -a]pyrazin- (4H)—yl](trifluorornethyl)benzonitrile; (7S)(2-Methoxypyridinyl)—7-methyl[4-(trifluorornethyl)phenyl]-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)(2-Ethylpyridinyl)rnethyl[4-(trifluorornethyl)phenyl]-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)[3-Chloro(trifluorornethyl)phenyl](2,6-dirnethylpyridinyl)rnethyl- 6,7-dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)(3,4-Dichlorophenyl)—3-(2,6-dirnethylpyridinyl)rnethyl-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)[2-(Ethylarnino)pyridinyl]rnethyl[4-(trifluorornethyl)phenyl]-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; 2014/061478 _ 13 _ (7S)Methyl(2-methylpyridinyl)-5 -[4-(trifluoromethoxy)phenyl] -6,7- opyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)[2-(Dimethylamino)pyridinyl]methyl[4-(trifluoromethyl)phenyl] -6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)(5-Chloroethoxypyridinyl)methyl(2-methylpyridinyl)-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl-3 -[2-(methylamino)pyridinyl] -5 -[4-(trifluoromethyl)phenyl] -6,7- dihydropyrazolo [1 ,5 azin-4(5H)-one; (7S)(3 ,4-Dichlorophenyl)(2-methoxypyridinyl)methyl-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(2-methylpyridinyl)-5 - {4-[(trifluoromethyl)sulfanyl]phenyl} -6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one or a hydrochloride salt thereof; 4- {(7S)Methyloxo[4-(trifluoromethyl)phenyl]-4,5 ,6,7-tetrahydropyrazolo[1 ,5- a]pyrazin-3 -yl}pyridinecarbonitrile; (7S)-5 -[3 -Chloro(trifluoromethyl)phenyl] -3 -(2-methoxypyridinyl)methyl-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -[3 -Chloro(trifluoromethyl)phenyl]methyl-3 -[2-(methylamino)pyridin yl]-6,7-dihydropyrazolo[1 ,5-a]pyrazin-4(5H)—one; (7S)-3 -(2-Azetidinylpyridinyl)methyl-5 - [4-(trifluoromethyl)phenyl] -6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl-5 -[4-(trifluoromethyl)phenyl] -3 rifluoromethyl)pyridinyl] -6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; 4- 5-[3 -Chloro(trifluoromethyl)phenyl]methyloxo-4,5 ,6,7- tetrahydropyrazolo [1 ,5 -a]pyrazin-3 -yl} (methylamino)pyridinecarbonitrile; (7S)(2-Methoxypyridinyl)—5 thoxy(trifluoromethyl)phenyl]methyl- 6,7-dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -[3 -Fluoro(trifluoromethyl)phenyl]methyl-3 -[2-(methylamino)pyridin yl]-6,7-dihydropyrazolo[1 ,5-a]pyrazin-4(5H)—one; and (7S)Methyl(2-methylpyridinyl)-5 - [5 -(trifluoromethyl)pyridinyl] -6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one.
In an additional embodiment, the t invention relates to compounds of Formula (I) as defined hereinabove, and stereoisomeric forms thereof, wherein R1 is phenyl, optionally substituted with one, two or three substituents each independently ed from the group of halo, C1_4alkyl, poly-haloC1_4alkyl, -O-C1_4alkyl, -C1_4alkyl-OH and cyano; or 2-pyridinyl, substituted with one or two substituents each independently selected from the group of halo, poly-haloC1_4alkyl, and -O-C1_4alkyl; R2 is wherein R5&1 is selected from hydrogen and C1_4alkyl, and R6&1 is selected from the group of hydrogen, C1_4alkyl, -C1_4alkyl-O-C1_4alkyl, -OC1_4alkyl, and -C1_4alkyl-OH; or wherein one of R5b and R6b is hydrogen, and the other R5b or R6b is C1_4alkyl; R3 is selected from hydrogen and C1_4alkyl; R4 is ed from the group of hydrogen, C1_4alkyl, mono- or poly-haloC1_4alkyl, and -C1_4alkyl-O-C1_4alkyl; in particular >CR3R4 is selected from the group of >CH2, >CH(CH3), >CH(CH2CH3), >CH(CH2F), >CH(CH20CH3) and >C(CH3)2; and the N—oxides, and the pharmaceutically acceptable salts and the solvates thereof.
In an additional embodiment, the present invention relates to nds of a (I) as defined hereinabove, and isomeric forms thereof, wherein R1 is phenyl, optionally substituted with one, two or three tuents each independently selected from the group of fluoro, , methyl, CF3, -O-CH3, -O-CH2CH3, cyano, -CH(CH3)(OH); or 2-pyridinyl, substituted with one or two substituents each independently ed from the group of fluoro, chloro, CF3, and -O-CH2CH3; R2 is R5a N R6a wherein R5&1 is selected from en and methyl, and R6&1 is selected from the group of hydrogen, methyl, -CH2-O-CH3, -O-CH3, and -CH2-OH; or wherein one of R5b and R6b is hydrogen, and the other R5b or R6b is methyl; W0 2014/195311 _ 15 _ R3 is selected from hydrogen and C1_4alkyl; R4 is selected from the group of hydrogen, C1_4alkyl, mono- or poly-haloC1_4alkyl, and -C1_4alkyl-O-C1_4alkyl; in particular >CR3R4 is ed from the group of >CH2, >CH(CH3), >CH(CH2CH3), >CH(CH2F), 20CH3) and >C(CH3)2; and the N—oxides, and the pharmaceutically acceptable salts and the es thereof.
In an additional embodiment, the present invention relates to compounds of Formula (I) as defined hereinabove, and stereoisomeric forms thereof, wherein R1 is (a) a phenyl substituent selected from the group of 9 F/: :'\\ \ "(2 ("U HQ "(3 (j \/O : O K) /0 Cl 0/\ F /0 F3C F ; ; \0 ; \O x ;and (b) a 2-pyridinyl substituent selected from the group of _ l6 _ F C3 CI N F306 \ \ N | l / | / 9 / .\ 9 I / x / and CI ; R2 is R5a N R68 wherein R5&1 is ed from hydrogen and methyl, and R6&1 is selected from the group of hydrogen, methyl, -CH2-O-CH3, -O-CH3, and -CH2-OH; or wherein one of R5b and R6b is hydrogen, and the other R5b or R6b is ; R3 is selected from hydrogen and C1_4alkyl; R4 is selected from the group of hydrogen, C1_4alkyl, mono- or poly-haloC1_4alkyl, and -C1_4alkyl-O-C1_4alkyl; in particular >CR3R4 is selected from the group of >CH2, >CH(CH3), 2CH3), >CH(CH2F), >CH(CH20CH3) and >C(CH3)2; and the N—oxides, and the pharmaceutically acceptable salts and the solvates thereof.
In an additional ment, the present invention relates to compounds selected from the group of (7S)Methyl(2-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo [l ,5 -a]pyrazin-4(5H)-one; (7S)Methylpyridinyl-5 -[4-(trifluoromethyl)phenyl]-6,7-dihydropyrazolo[ l ,5 - a]pyrazin-4(5H)-one; (7S)[2-(Methoxymethyl)pyridinyl]methyl[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo [l ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(5-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- opyrazolo [l ,5 -a]pyrazin-4(5H)-one; (7R)Methyl(2-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- W0 95311 _ 17 _ opyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7R)-5 - [3 -Eth0xy(trifluor0rnethy1)pheny1]methy1-3 -(2-methy1pyridiny1)—6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; - [3 -Ethoxy(trifluor0rnethy1)pheny1]-3 -(2-methy1pyridiny1)-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(4-Methoxy-3 ,5-dimethylpheny1)methy1-3 -(2-methy1pyridiny1)—6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methy1(6-methy1pyridin-3 -y1)-5 - [4-(triflu0romethy1)pheny1]-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 thoxypheny1)rnethy1-3 -(2-methy1pyridiny1)-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; 3 -(2-Methy1pyridiny1)-5 - [4-(triflu0r0rnethy1)pheny1]-6 5 - , 7-dihydropyraz010[1 , a]pyrazin-4(5H)-one; (7S)-5 -(3 eth0xypheny1)rnethy1-3 -(2-rnethy1pyridiny1)—6,7 - dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-3 thoxypyridiny1)—7-rnethy1-5 - [4-(triflu0romethy1)pheny1]-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methy1-5 -(4-rnethy1pheny1)-3 -(2-methy1pyridiny1)-6 ,7-dihydropyraz010[1 ,5 - a]pyrazin-4(5H)-one; (7S)Methy1-5 - [3 -(1-rnethylethoxy)pheny1]-3 -(2-rnethy1pyridiny1)-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; 4- [(7S)Methy1-3 -(2-rnethy1pyridiny1)0X0-6,7-dihydr0pyraz010[1,5 -a]pyrazin- (4H)-y1]benzonitrile; (7S)-5 -(4-Eth0xypheny1)rnethy1-3 -(2-methy1pyridiny1)-6 ,7-dihydropyraz010[1 ,5 - a]pyrazin-4(5H)-one; (7S)-5 -(3 ,5 -Diflu0r0pheny1)rnethy1-3 -(2-rnethy1pyridiny1)-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 -Eth0xypheny1)rnethy1-3 -(2-methy1pyridiny1)-6,7-dihydr0pyraz010[1 ,5 - a]pyrazin-4(5H)-one; (7S)-5 -(3 ,4-Difluor0rnethoxypheny1)—7-methy1-3 -(2-methy1pyridiny1)-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 -F1uor0-5 -rnethoxypheny1)—7-methy1-3 -(2-methy1pyridiny1)—6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methy1-3 ethy1pyridiny1)pheny1-6,7-dihydr0pyraz010[1 ,5 -a]pyrazin- 4(5H)—one; (7S)-5 -[4-(1-Hydr0xyethy1)pheny1]rnethy1-3 ethy1pyridiny1)—6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; _ 18 _ (7R)-5 -(3 ,4-Dich10r0pheny1)(flu0r0rnethy1)-3 -(2-rnethy1pyridiny1)—6,7 - dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-0ne; (7R)-5 -(3 ,4-Dich10r0pheny1)(rnethoxymethy1)-3 -(2-rnethy1pyridiny1)-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-0ne; and (7S)-5 -(3 ,4-Dich10r0pheny1)—3 - [2-(hydr0xymethy1)pyridiny1] rnethy1-6 ,7- dihydropyrazolo [1 ,5 azin-4(5H)-0ne; (7R)Ethy1-3 -(2-rnethy1pyridiny1)-5 -[4-(trifluoromethy1)pheny1]-6 ,7- opyrazolo [1 ,5 -a]pyrazin-4(5H)-0ne; (7S)Methy1-3 - [2-(rnethy1arnin0)pyridiny1] -5 -[4-(trifluoromethy1)pheny1]-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-0ne; (7S)-5 -[3 dr0xyethy1)pheny1]rnethy1-3 -(2-rnethy1pyridiny1)—6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-0ne; (7S)-5 -(4-Ch10r0rneth0xypheny1)rnethy1-3 -(2-rnethy1pyridiny1)-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-0ne; (7S)(2,4-Dich10r0pheny1)—7-rnethy1-3 -(2-methy1pyridiny1)-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-0ne; 7 - [4 -(triflu0r0rnethy1)pheny1]-6,7- , 7-Dirnethy1-3 ethy1pyridiny1)-5 dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-0ne; (7S)-5 -(4-Ch10r0rnethy1pheny1)rnethy1-3 -(2-rnethy1pyridiny1)-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-0ne; (7S)Methy1-3 -(2-rnethy1pyridiny1)-5 - [5 -(trifluorornethy1)pyridiny1] -6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-0ne; (7S)-5 -(5 -Ch10r0pyridiny1)rnethy1-3 -(2-rnethy1pyridiny1)-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-0ne; (7S)Methy1pyridiny1-5 -[5 -(trifluoromethy1)pyridiny1] -6 ,7- opyrazolo [1 ,5 -a]pyrazin-4(5H)-0ne; (7S)-5 -(5 yfluor0pyridiny1)rnethy1-3 -(2-rnethy1pyridiny1)-6 ,7- dihydropyrazolo [1 ,5 azin-4(5H)-0ne; (7S)-3 -(2,6-Dirnethy1pyridiny1)rnethy1-5 -[5 -(trifluoromethy1)pyridiny1]-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-0ne; (7S)-5 -(3 -Ch10r0ethoxypyridiny1)—7-rnethy1-3 -(2-methy1pyridiny1)-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-0ne; and (7S)-5 -[6-Eth0xy-5 -(trifluorornethy1)pyridiny1] rnethy1-3 -(2-rnethy1pyridiny1)- 6 5 -a]pyrazin-4(5H)-one; , dr0pyraz010 [1 , and the N—oxides, and the pharmaceutically acceptable salts and the solvates thereof.
WO 95311 _ 19 _ In an additional embodiment, the present invention relates to compounds selected from the group of (7S)Methyl(2-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[l,5-a]pyrazin-4(5H)-one, or a hydrochloride salt, or a sulfate salt, or a methanesulfonate salt, or a maleate salt thereof; (7S)Methylpyridinyl-5 rifluoromethyl)phenyl]-6,7-dihydropyrazolo[ l ,5 - a]pyrazin-4(5H)-one; (7S)[2-(Methoxymethyl)pyridinyl]methyl[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[l ,5-a]pyrazin-4(5H)-one or a hydrochloride salt thereof; (7S)Methyl(5-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo [l ,5 -a]pyrazin-4(5H)-one; (7R)Methyl(2-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo [l ,5 -a]pyrazin-4(5H)-one; -[3 -Ethoxy(trifluoromethyl)phenyl]methyl(2-methylpyridinyl)—6,7- opyrazolo [l ,5 -a]pyrazin-4(5H)-one; -[3 -Ethoxy(trifluoromethyl)phenyl](2-methylpyridinyl)-6,7- dihydropyrazolo [l ,5 -a]pyrazin-4(5H)-one; -(4-Methoxy-3,5-dimethylphenyl)methyl(2-methylpyridinyl)—6,7- dihydropyrazolo [l ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(6-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo [l ,5 -a]pyrazin-4(5H)-one; (7S)(4-Methoxyphenyl)methyl(2-methylpyridinyl)-6,7- dihydropyrazolo [l ,5 -a]pyrazin-4(5H)-one; 3 -(2-Methylpyridinyl)-5 - [4-(trifluoromethyl)phenyl] -6,7-dihydropyrazolo[ l ,5 - a]pyrazin-4(5H)-one; (7S)(3,4-Dimethoxyphenyl)methyl(2-methylpyridinyl)—6,7- opyrazolo [l ,5 -a]pyrazin-4(5H)-one; (7S)(2-Methoxypyridinyl)—7-methyl[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo [l ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(4-methylphenyl)(2-methylpyridinyl)-6,7-dihydropyrazolo[ l ,5 - a]pyrazin-4(5H)-one; (7S)Methyl-5 - [3 -( l -methylethoxy)phenyl] -3 -(2-methylpyridinyl)-6,7- dihydropyrazolo[l ,5-a]pyrazin-4(5H)-one or a hydrochloride salt thereof; 4- [(7S)Methyl(2-methylpyridinyl)oxo-6,7-dihydropyrazolo[ l ,5 -a]pyrazin- (4H)—yl]benzonitrile; -(4-Ethoxyphenyl)methyl(2-methylpyridinyl)-6,7-dihydropyrazolo[ l ,5 - a]pyrazin-4(5H)-one or a hydrochloride salt thereof; WO 95311 _ 20 _ (7S)-5 -(3 ,5 -Diflu0r0pheny1)rnethy1-3 -(2-rnethy1pyridiny1)-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 -Eth0xypheny1)rnethy1-3 -(2-methy1pyridiny1)-6,7-dihydr0pyraz010[1 ,5 - a]pyrazin-4(5H)-one; (7S)-5 -(3 uor0rnethoxypheny1)—7-methy1-3 -(2-methy1pyridiny1)-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 -F1uor0-5 -rnethoxypheny1)—7-methy1-3 -(2-methy1pyridiny1)—6,7- opyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methy1-3 -(2-rnethy1pyridiny1)pheny1-6,7-dihydr0pyraz010[1 ,5 -a]pyrazin- 4(5H)—one; (7S)-5 -Hydr0xyethy1)pheny1]rnethy1-3 -(2-rnethy1pyridiny1)—6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7R)-5 -(3 ,4-Dich10r0pheny1)(flu0r0rnethy1)-3 -(2-rnethy1pyridiny1)—6,7 - dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7R)-5 -(3 h10r0pheny1)(rnethoxymethy1)—3 -(2-methy1pyridiny1)-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; and (7S)-5 -(3 ,4-Dich10r0pheny1)—3 - [2-(hydr0xymethy1)pyridiny1] rnethy1-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7R)Ethy1-3 -(2-rnethy1pyridiny1)-5 -[4-(trifluoromethy1)pheny1]-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methy1-3 - [2-(rnethy1arnino)pyridiny1] -5 -[4-(trifluoromethy1)pheny1]-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -[3 -(1-Hydr0xyethy1)pheny1]rnethy1-3 ethy1pyridiny1)—6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(4-Ch10r0methoxypheny1)rnethy1-3 -(2-rnethy1pyridiny1)-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(2,4-Dich10r0pheny1)—7-methy1-3 -(2-rnethy1pyridiny1)-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; 7 - [4-(triflu0romethy1)pheny1]-6,7- , 7-Dirnethy1-3 -(2-rnethy1pyridiny1)-5 dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(4-Ch10r0rnethy1pheny1)rnethy1-3 -(2-methy1pyridiny1)-6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methy1-3 ethy1pyridiny1)-5 - [5 -(trifluor0rnethy1)pyridiny1] -6 ,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(5 -Ch10r0pyridiny1)rnethy1-3 -(2-rnethy1pyridiny1)-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methy1pyridiny1-5 -[5 -(trifluoromethy1)pyridiny1] -6 ,7- WO 95311 _ 21 _ dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)(5-Ethoxyfluoropyridinyl)methyl(2-methylpyridinyl)-6,7- dihydropyrazolo [1 ,5 azin-4(5H)-one; (7S)(2,6-Dimethylpyridinyl)methyl[5-(trifluoromethyl)pyridinyl]-6,7- dihydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)(3-Chloroethoxypyridinyl)—7-methyl(2-methylpyridinyl)-6,7- dihydropyrazolo[1 ,5-a]pyrazin-4(5H)-one; and (7S)[6-Ethoxy(trifluoromethyl)pyridinyl]methyl(2-methylpyridinyl)— hydropyrazolo [1 ,5 -a]pyrazin-4(5H)-one; and the pharmaceutically acceptable salts and the solvates thereof.
In an additional embodiment, the present invention relates to compounds selected from the group of (7S)Methyl(2-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[l,5-a]pyrazin-4(5H)-one, or a hydrochloride salt, or a sulfate salt, or a methanesulfonate salt, or a maleate salt thereof; (7S)Methylpyridinyl-5 -[4-(trifluoromethyl)phenyl]-6,7-dihydropyrazolo [1 ,5 - a]pyrazin-4(5H)-one; -[2-(Methoxymethyl)pyridinyl]methyl[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[l,5-a]pyrazin-4(5H)-one or a hydrochloride salt thereof; (7R)—7-Methyl(2-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7R)[3-Ethoxy(trifluoromethyl)phenyl]methyl-3 -(2-methylpyridinyl)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; -[3-Ethoxy(trifluoromethyl)phenyl](2-methylpyridinyl)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)(4-Methoxy-3,5-dimethylphenyl)methyl(2-methylpyridinyl)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(6-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)(4-Methoxyphenyl)methyl(2-methylpyridinyl)—6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; 3 -(2-Methylpyridinyl)-5 -[4-(trifluoromethyl)phenyl]-6,7-dihydropyrazolo [1 ,5 - zin-4(5H)-one; (7S)(3,4-Dimethoxyphenyl)methyl(2-methylpyridinyl)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)(2-Methoxypyridinyl)methyl[4-(trifluoromethyl)phenyl]-6,7- _ 22 _ dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methy1—5-[3-(1 -rnethy1ethoxy)phenyl](2-rnethylpyridiny1)-6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-one or a hydrochloride salt thereof; 4-[(7S)Methy1-3 -(2-rnethy1pyridiny1)oxo-6,7-dihydropyrazolo [1 ,5 - a]pyrazin-5(4H)-y1]benzonitrile; (7S)(4-Ethoxypheny1)rnethy1(2-rnethy1pyridinyl)—6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-one or a hydrochloride salt thereof; (7S)(3,5-Difluoropheny1)—7-rnethy1(2-rnethy1pyridiny1)—6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)(3 -Ethoxypheny1)rnethy1(2-rnethy1pyridiny1)—6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)(3,4-Difluorornethoxyphenyl)rnethy1—3-(2-rnethylpyridiny1)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)(3 -F1uorornethoxypheny1)rnethy1(2-rnethy1pyridiny1)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; -[4-(1-Hydroxyethyl)pheny1]rnethy1—3 -(2-rnethylpyridiny1)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7R)(3,4-Dichloropheny1)—7-(rnethoxyrnethyl)(2-rnethy1pyridinyl)-6,7- dihydropyrazolo[1 ,5-a]pyrazin-4(5H)-one; and (7S)(3,4-Dichloropheny1)[2-(hydroxymethyl)pyridinyl]rnethy1—6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methy1—3-[2-(methylarnino)pyridinyl][4-(trifluorornethy1)phenyl]-6,7- opyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [3 -(1 -Hydroxyethyl)pheny1]rnethy1—3 -(2-rnethylpyridiny1)-6,7- opyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)(4-Chlorornethoxyphenyl)—7-methyl(2-rnethylpyridiny1)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)(2,4-Dichlorophenyl)rnethy1—3-(2-rnethylpyridinyl)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; 7,7-Dirnethyl(2-rnethy1pyridinyl)[4-(trifluorornethyl)phenyl]-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; -(4-Chlorornethy1pheny1)rnethy1—3-(2-rnethylpyridinyl)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(2-rnethylpyridinyl)[5-(trifluorornethyl)pyridiny1]-6,7- dihydropyrazolo[1 ,5 azin-4(5H)-one; (7S)(5-Chloropyridiny1)rnethy1—3-(2-rnethy1pyridinyl)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methylpyridinyl-5 - [5 -(trifluoromethyl)pyridinyl] -6,7- dihydropyrazolo[ l ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(5 -Ethoxyfluoropyridinyl)methyl-3 -(2-methylpyridinyl)-6,7- dihydropyrazolo[ l ,5 -a]pyrazin-4(5H)-one; (7S)-3 -(2 ,6-Dimethylpyridinyl)methyl-5 - [5 uoromethyl)pyridinyl] -6 ,7- dihydropyrazolo[ l ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 -Chloroethoxypyridinyl)methyl-3 -(2-methylpyridinyl)-6 ,7- dihydropyrazolo[ l ,5 -a]pyrazin-4(5H)-one; and (7S)-5 - oxy-5 -(trifluoromethyl)pyridinyl] methyl-3 thylpyridin yl)-6 ,7-dihydropyrazolo[ l ,5 -a]pyrazin-4(5H)-one.
In an onal embodiment, the present invention relates to compounds of Formula (I) as defined hereinabove, and stereoisomeric forms thereof, wherein R1 is phenyl, optionally substituted with one or more substituents each independently selected from the group of halo, C1_4alkyl, mono- or poly-haloC1_4alkyl, -O-C1_4alkyl, mono- or aloC1_4alkyloxy, cyano and —SF5; or is CEO/ R2 is selected from R6 R5 i and : wherein R5 and R6 are each independently selected from the group of hydrogen, C1_4alkyl, mono- or poly-haloC1_4alkyl, -C1_4alkyl-O-C1_4alkyl, -O-C1_4alkyl, and NR’R"; wherein R’ is selected from hydrogen and C1_4alkyl; R" is selected from en and C1_4alkyl; R3 is selected from en and C1_4alkyl; R4 is selected from the group of hydrogen, C1_4alkyl, mono- or poly-haloC1_4alkyl, -C1_4alkyl-O-C1_4alkyl, and -C1_4alkyl-OH; and the pharmaceutically acceptable salts and the solvates f.
In an additional embodiment, the present invention relates to compounds of Formula (I) as defined hereinabove, and stereoisomeric forms thereof, wherein R1 is phenyl, optionally substituted with one or more substituents each independently selected from the group of halo, C1_4alkyl, mono- or poly-haloC1_4alkyl, -O-C1_4alkyl, mono- or poly-haloC1_4alkyloxy, cyano and —SF5; or is @131in particular "(1:1 , ; R2 is selected from R5 R5 : and : wherein R5 and R6 are each independently selected from the group of hydrogen, C1_4alkyl, -C1_4alkyl-O-C1_4alkyl, 4alkyl, and NR’R"; wherein R’ is hydrogen; R" is hydrogen; R3 is selected from hydrogen and C1_4alkyl; R4 is ed from the group of hydrogen and C1_4alkyl; and the pharmaceutically able salts and the solvates thereof.
In an additional embodiment, the present invention relates to compounds of Formula (I) as defined hereinabove, and stereoisomeric forms thereof, wherein R1 is phenyl, optionally substituted with one or more substituents each independently selected from the group of halo, C1_4alkyl, aloC1_4alkyl and —SF5; R2 is selected from 6 5 R N R R |\ P" / / and ' wherein R5 and R6 are each independently selected from the group of hydrogen, C1_4alkyl and 4alkyl; R3 is selected from en and C1_4alkyl; R4 is hydrogen; and the pharmaceutically acceptable salts and the solvates thereof.
In an additional embodiment, the present invention relates to compounds of Formula (I) as defined hereinabove, and stereoisomeric forms thereof, wherein R1 is phenyl, ally substituted with one or more substituents each independently selected from the group of halo, C1_4alkyl, poly-haloC1_4alkyl and —SF5; R2 is selected from 6 5 R N R R |\ P" / / and ' wherein R5 and R6 are each independently selected from the group of hydrogen, C1_4alkyl and -O-C1_4alkyl; R3 is hydrogen; R4 is selected from hydrogen and C1_4alkyl; and the pharmaceutically able salts and the solvates thereof.
In an additional embodiment, the t invention relates to compounds of Formula (I) as defined above, and stereoisomeric forms thereof, wherein R1 is phenyl, substituted with one, two or three substituents each independently selected from the group of halo, and poly-haloC1_4alkyl; R2 is wherein R5 and R6 are each independently selected from the group of hydrogen, C1_4alkyl, -O-C1_4alkyl, and NR’R"; n R’ is hydrogen; R" is C1_4alkyl; R3 is en; R4 is hydrogen or C1_4alkyl; in particular R4 is C1_4alkyl; and the pharmaceutically acceptable salts and the solvates f.
In an additional embodiment, R1 is selected from the group of F CI F3C\© F3C\ i F3C\ i 9 9 WO 95311 flab /\O F3C\© F Sc :5 CI CF3 CI\© Ob C|\ i ; and \- and the rest of variables are as defined in Formula (I) herein.
In an additional embodiment, R1 is selected from the group of F CI FC3 \© F30, i F3C\ i \g ‘~;and and the rest of variables are as defined in a (I) herein; and the pharmaceutically acceptable salts and the solvates thereof.
In a further embodiment, the present invention relates to nds of Formula (I) as defined herein wherein R3 is hydrogen and R4 is a substituent different from hydrogen having a configuration as ed in the Formula (1’) below, wherein the hydropyrazolo[l,5-a]pyrazin-4(5H)—one core, R1 and R2 are in the plane of the drawing and R4 is projected above the plane of the drawing (bond shown with a bold wedge), and the rest of variables are as defined in Formula (I) herein R4 (1’).
In a yet further embodiment, the present invention relates to compounds of Formula (I) as defined herein wherein R4 is hydrogen and R3 is a substituent different from en, for example a C1_4alkyl substituent having a configuration as depicted in the Formula (1") below, wherein the 6,7-dihydropyrazolo[l,5-a]pyrazin-4(5H)-one core, R1 and R2 are in the plane of the drawing and R3 is projected above the plane of the drawing (bond shown with a bold wedge), and the rest of variables are as defined in Formula (I) herein 0 R2 R\N% R (13,)- In an additional ment, the present invention relates to compounds of Formula (I’) as defined hereinabove, and stereoisomeric forms f, wherein R1 is , substituted with one or two substituents each ndently selected from the group of halo, and aloC1_4alkyl; R2 is wherein R5 and R6 are each independently selected from the group of hydrogen, C1_4alkyl, -O-C1_4alkyl, and NR’R"; wherein R’ is hydrogen; R" is C1_4alkyl; R4 is hydrogen or C1_4alkyl; in particular R4 is C1_4alkyl, more in particular methyl; and the pharmaceutically acceptable salts and the solvates thereof.
In an onal embodiment, the present invention relates to compounds of Formula (I’) as defined hereinabove, and isomeric forms thereof, wherein R1 is phenyl, substituted with one or two substituents each independently selected from the group of halo, and poly-haloC1_4alkyl; R2 is wherein one of R5 and R6 is hydrogen or methyl, in ular hydrogen; and the other one of R5 or R6 is selected from the group of C1_4alkyl, -O-C1_4alkyl, and NR’R"; wherein R’ is hydrogen; R" is C1_4alkyl; R4 is hydrogen or C1_4alkyl; in particular R4 is C1_4alkyl, more in particular methyl; and the pharmaceutically acceptable salts and the solvates thereof.
Specific compounds according to the invention include: _ 28 _ (7S)Methyl(2-methy1pyridinyl)-5 -[4-(trifluorornethyl)phenyl] -6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methylpyridiny1—5 - [4-(trifluoromethy1)phenyl] -6 ,7-dihydr0pyrazolo [1 ,5 - a]pyrazin-4(5H)-one; (7S)-5 - [3 -Ch10r0(triflu0r0rnethyl)phenyl] thy1—3 -(2-rnethy1pyridiny1)—6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(2-methy1pyridinyl)-5 -[4-(pentafluoro-}\6-sulfanyl)phenyl] -6,7 - dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(2-methy1pyridinyl)-5 -[3 -rnethy1—4-(trifluorornethyl)phenyl]-6 ,7- opyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 ,4-Dichlor0phenyl)—7-methy1-3 -(2-rnethylpyridinyl)-6 ,7- dihydropyrazolo[1 ,5 azin-4(5H)-one; (7S)-5 -(4-Ch10r0-3 -rnethylphenyl)rnethyl-3 -(2-rnethy1pyridinyl)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [3 -Ethoxy(trifluorornethyl)phenyl] rnethy1—3 -(2-rnethylpyridinyl)-6 ,7- opyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [4-Chloro-3 -(triflu0r0rnethyl)phenyl] rnethy1—3 -(2-rnethy1pyridiny1)—6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [3 -F1u0r0(trifluor0rnethyl)phenyl] rnethy1—3 -(2-rnethy1pyridinyl)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; 7-Methy1-3 -(2-rnethylpyridiny1)-5 -[4-(trifluor0rnethy1)phenyl] -6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [3 -Meth0xy(trifluor0rnethyl)phenyl] rnethy1—3 -(2-rnethylpyridiny1)- hydr0pyrazolo[1 5 -a]pyrazin-4(5H)-one; - [(7S)—7-Methyl-3 -(2-rnethy1pyridinyl)0x0-6,7-dihydr0pyrazolo[1 5 -a]pyrazin- (4H)-y1] (trifluorornethyl)benzonitrile; (7S)-3 -(2,6-Dirnethylpyridiny1)rnethyl-5 -[4-(trifluorornethyl)phenyl] -6 ,7- dihydropyrazolo[1 ,5 azin-4(5H)-one; (7S)-5 -(4-Chlor0phenyl)rnethy1—3 -(2-rnethylpyridinyl)-6 ,7-dihydropyrazolo[1 ,5 - a]pyrazin-4(5H)-one; (7S)-5 -(3 -Ch10r0phenyl)rnethy1—3 -(2-rnethylpyridinyl)-6 ydropyrazolo[1 ,5 - zin-4(5H)-one; (7S)-5 -(3 -Ch10r0eth0xyphenyl)rnethy1—3 -(2-rnethy1pyridinyl)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(4-Ch10r0-3 -ethoxyphenyl)rnethyl-3 -(2-rnethy1pyridinyl)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(4-Ch10r0-3 -rnethoxyphenyl)—7-rnethyl-3 -(2-rnethylpyridiny1)-6,7 - _ 29 _ dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)(3 -Ch10r0methoxypheny1)—7-methy1—3-(2-rnethylpyridiny1)—6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)(4-F1u0ro-3 -rnethylpheny1)rnethy1—3-(2-methylpyridinyl)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)[2-(Meth0xymethyl)pyridinyl]rnethy1[4-(triflu0romethyl)phenyl]-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(2-rnethylpyridinyl)[3-(trifluorornethy1)phenyl]-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(5-rnethylpyridiny1)[4-(trifluorornethy1)phenyl]-6,7- opyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)(3,4-Difluor0phenyl)rnethyl(2-rnethylpyridiny1)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7R)Methy1—3-(2-rnethylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; -[4-(Diflu0r0rnethoxy)phenyl]rnethyl(2-rnethylpyridinyl)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)(4-Fluorophenyl)rnethyl(2-rnethylpyridinyl)-6,7-dihydropyrazolo[1,5- a]pyrazin-4(5H)-one; (7S)(5,6-Dimethylpyridin-3 -y1)rnethyl[4-(trifluor0rnethyl)phenyl]-6,7- opyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)(4-Ch10rofluor0phenyl)rnethyl(2-rnethylpyridinyl)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7R)[3-Eth0xy(trifluoromethyl)phenyl]rnethyl(2-rnethylpyridinyl)-6,7- dihydropyrazolo[ 1 ,5 azin-4(5H)-one; (7S)Methylpyridinyl[4-(trifluor0rnethyl)pheny1]-6,7-dihydropyrazolo[1 ,5- a]pyrazin-4(5H)-one; -[3-Eth0xy(trifluoromethyl)phenyl](2-rnethylpyridinyl)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)(4-Methoxy-3,5-dimethylphenyl)—7-methy1(2-methylpyridiny1)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)(3-F1uor0methoxyphenyl)methyl(2-methy1pyridinyl)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; -Methyl(6-rnethylpyridiny1)[4-(trifluorornethy1)phenyl]-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)(6-Arnin0pyridiny1)rnethyl[4-(trifluor0rnethyl)phenyl]-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(4-Methoxyphenyl)rnethy1-3 -(2-rnethylpyridinyl)-6,7- dihydropyrazolo[1 ,5 azin-4(5H)-one; - [3 -F1u0r0(trifluoromethyl)phenyl] -3 -(2-rnethylpyridinyl)-6 7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; 3 -(2-Methylpyridinyl)-5 -[4-(trifluor0rnethyl)phenyl] -6,7-dihydr0pyrazolo [1 5 - a]pyrazin-4(5H)-one; (7S)-5 -(3 ,4-Dimethoxyphenyl)rnethyl-3 -(2-rnethy1pyridinyl)—6,7 - dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(2 ,3 -Dihydr0-1 ,4-benz0dioxiny1)rnethyl-3 -(2-rnethylpyridiny1)-6 ,7- dihydropyrazolo[1 ,5 azin-4(5H)-one; (7S)-5 - [3 -ch10r0(trifluor0rnethyl)phenyl] -3 -(2,6-dimethylpyridy1)—7-rnethyl-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazinone; (7S)-3 - [2-(ethylarnino)pyridyl] rnethy1—5 - [4-(trifluor0rnethyl)phenyl] -6,7- dihydropyrazolo[ 1 ,5 -a]pyrazinone; (7S)-3 -(2-rnethoxypyridy1)rnethyl-5 - [4-(trifluor0rnethyl)phenyl] -6,7- dihydropyrazolo[ 1 ,5 -a]pyrazinone; (7S)-3 -(2-ethylpyridy1)rnethyl-5 - [4-(trifluor0rnethyl)phenyl] -6 ,7- dihydropyrazolo[ 1 ,5 -a]pyrazinone; (7S)-5 -(3 ,4-dichlorophenyl)-3 -(2,6-dirnethy1—4-pyridy1)rnethy1—6,7- dihydropyrazolo[ 1 ,5 -a]pyrazinone; (7S)-5 - [3 -(2-F1u0r0ethoxy)(trifluor0rnethy1)phenyl] rnethy1-3 -(2-rnethylpyridin- 4-y1)-6,7-dihydr0pyrazolo[1 ,5-a]pyrazin-4(5H)-one; (7S)-3 -(2 ,6-dirnethylpyridy1)-5 -[3 y(trifluorornethyl)phenyl] rnethy1— 6,7-dihydropyrazolo[1 5 -a]pyrazin0ne; (7S)-5 - [3 -ch10r0(trifluor0rnethyl)phenyl] rnethy1—3 -(4-pyridy1)-6 ,7- dihydropyrazolo[ 1 ,5 azinone; (7S)-3 -(2 ,6-dirnethylpyridy1)-5 -[3 -methoxy(triflu0rornethyl)pheny1]rnethy1— 6,7-dihydropyrazolo[1 5 -a]pyrazin0ne; 7-(flu0rornethyl)—3 -(2-rnethy1—4-pyridy1)—5 -[4-(trifluor0rnethyl)phenyl] -6 ,7- dihydropyrazolo[ 1 ,5 -a]pyrazinone; (7S)-3 -(2 ,6-dirnethylpyridyl)rnethyl-5 entafluoro- k6-sulfanyl)phenyl] -6,7- dihydropyrazolo[ 1 ,5 azinone; (7S)-5 - [4-ch10r0-3 -(trifluor0rnethyl)phenyl] -3 -(2,6-dimethylpyridy1)—7-rnethyl-6,7- dihydropyrazolo[ 1 ,5 azinone; (7S)-5 - [3 -ethoxy(triflu0rornethyl)phenyl] rnethy1—3 -(4-pyridy1)-6,7- opyrazolo[ 1 ,5 -a]pyrazinone; (7S)methyl-5 - [4-(pentafluoro-W—sulfany1)phenyl] -3 -(4-pyridy1)-6 ,7- _ 31 _ dihydropyrazolo[ 1 ,5 -a]pyrazinone; (7S)-5 -(3 ,4-dichloropheny1)rnethyl-3 -(4-pyridy1)—6,7-dihydropyrazolo[ 1 ,5 - zinone; (7S)methyl-3 -(2-rnethy1—4-pyridy1)-5 - [3 -(trifluoromethoxy)phenyl] -6,7- dihydropyrazolo[ 1 ,5 -a]pyrazinone; -[(7 S)-3 -(2,6-dimethylpyridy1)—7-rnethyloxo-6,7-dihydr0pyrazolo[1 ,5 - a]pyrazin-5 -y1] (trifluorornethyl)benzonitrile; (7S)-5 - [3 (trifluorornethyl)phenyl] thy1—3 -(4-pyridyl)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazinone; (7S)-3 -(2 ,6-dirnethylpyridy1)-5 -[3 -fluor0(trifluoromethyl)phenyl] rnethyl-6 ,7- dihydropyrazolo[ 1 ,5 -a]pyrazinone; (7S)-5 -(4-Ch10r0-3 -flu0r0pheny1)rnethy1—3 -(2-rnethy1pyridinyl)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 -chloro-5 -fluoro-pheny1)rnethy1—3 -(2-rnethy1—4-pyridyl)-6 ,7- opyrazolo[ 1 ,5 azinone; (7S)-5 - [3 -rneth0xy(triflu0romethyl)phenyl] rnethy1—3 ridyl)-6 ,7- dihydropyrazolo[ 1 ,5 -a]pyrazinone; (7S)-5 -(4-isopr0pylpheny1)rnethyl-3 -(2-rnethy1pyridyl)-6 ,7- dihydropyrazolo[ 1 ,5 -a]pyrazinone; (7S)methyl-3 -(2-rnethy1—4-pyridy1)-5 -(4-pr0pylphenyl)-6 ,7-dihydropyrazolo[1 ,5 - a]pyrazinone; (7S)-5 - [4-F1uoro-3 -(triflu0r0rnethyl)phenyl] rnethy1—3 -(2-rnethy1pyridinyl)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [4-ch10r0-3 -(trifluor0rnethyl)phenyl] rnethy1—3 ridy1)-6 ,7- dihydropyrazolo[ 1 ,5 -a]pyrazinone; (7S)-5 - [3 -(difluorornethoxy)-5 -fluoro-pheny1]rnethy1—3 -(2-rnethy1—4-pyridyl)—6,7 - dihydropyrazolo[ 1 ,5 -a]pyrazinone; 7-ethyl-3 -(2-rnethy1pyridyl)-5 -[4-(trifluor0rnethyl)phenyl] -6,7- dihydropyrazolo[ 1 ,5 -a]pyrazinone; (7S)-3 -(2-Arnin0pyridinyl)rnethy1—5 rifluorornethyl)phenyl] -6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(4-ch10r0pheny1)-3 -(2,6-dimethy1pyridy1)—7-rnethy1—6,7- dihydropyrazolo[ 1 ,5 -a]pyrazinone; (7S)-5 -(4-chlorophenyl)rnethy1—3 -(4-pyridy1)-6,7-dihydropyrazolo[1 ,5 -a]pyrazin- 4-one; - [3 -Eth0xy(trifluorornethyl)phenyl](hydr0xymethyl)-3 -(2-rnethylpyridinyl)- 6,7-dihydr0pyrazolo[1 5 -a]pyrazin-4(5H)-one; 2-F1u0r0[(7S)rnethy1(2-rnethy1pyridiny1)—4-0X0-6,7-dihydr0pyraz010[1,5- a]pyrazin-5 1]benzonitrile; (7S)-5 -(3 -F1uorornethy1pheny1)rnethy1-3 -(2-methy1pyridiny1)-6,7- dihydropyraz010[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [4-(2—fluor0ethoxy)-3 uorornethy1)pheny1]rnethy1-3 -(2-rnethy1 pyridy1)-6,7-dihydropyraz010[1 ,5 -a]pyrazin0ne; (7S)Methy1(4-rnethy1pheny1)-3 -(2-methy1pyridiny1)—6,7- opyraz010[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)Methy1[3-(1 -rnethylethoxy)pheny1](2-rnethy1pyridiny1)—6,7- dihydropyraz010[ 1 ,5 -a]pyrazin-4(5H)-one; 4-[(7S)Methy1-3 -(2-rnethy1pyridiny1)—4-0X0-6,7-dihydropyraz010 [1 ,5 -a]pyrazin- (4H)-y1]benz0nitrile; (7S)(4-Eth0xypheny1)rnethy1-3 -(2-methy1pyridiny1)—6,7- opyraz010[ 1 ,5 azin-4(5H)-one; (7S)(3 ,5-Diflu0r0pheny1)—7-methy1(2-rnethy1pyridiny1)—6,7- dihydropyraz010[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 -Ethoxypheny1)methy1-3 -(2-methy1pyridiny1)—6,7- dihydropyraz010[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 ,4-diflu0r0-5 -rneth0xy-pheny1)rnethy1-3 -(2-rnethy1pyridy1)—6,7- dihydropyraz010[ 1 ,5 -a]pyrazinone; (7S)-5 -(3 -fluoro-5 -rnethoxy-pheny1)rnethy1-3 -(2-rnethy1pyridy1)-6,7- dihydropyraz010[ 1 ,5 -a]pyrazinone; (7S)Methy1(2-rnethy1pyridiny1)pheny1-6,7-dihydr0pyraz010 [1 ,5 -a]pyrazin- 4(5H)-one; roxymethy1)(2-rnethy1pyridy1)[4-(triflu0romethy1)pheny1]-6,7- dihydropyraz010[ 1 ,5 -a]pyrazinone; -[(7 S)-3 -(2-Meth0xypyridiny1)rnethy10X0-6,7-dihydr0pyraz010 [1 ,5 - a]pyrazin-5 (4H)-y1] (trifluoromethy1)benzonitrile; (7S)(4-Ch10r0pheny1)(2-rneth0xypyridiny1)rnethy1-6,7- dihydropyraz010[ 1 ,5 -a]pyrazin-4(5H)-one; -(3 ,4-Dich10r0pheny1)—3 - [2-(dirnethy1arnino)pyridiny1] (flu0rornethy1)-6,7- dihydropyraz010[ 1 yrazin-4(5H)-0ne (7R or 78); -(3 ,4-Dich10r0pheny1)—3 - [2-(dirnethy1arnino)pyridiny1] (flu0rornethy1)-6,7- dihydropyraz010[1,5-a]pyrazin-4(5H)-0ne (78 or 7R); (7S)-5 - [3 -Ch10r0(triflu0rornethy1)pheny1]-3 -[2-(3 -fluor0azetidiny1)pyridin y1] rnethy1-6,7-dihydr0pyraz010 [1 ,5 -a]pyrazin-4(5H)-one; -(3 ,4-Dich10r0pheny1)—7-(fluoromethy1)-3 -[2-(methylarnino)pyridiny1] -6,7- 2014/061478 _ 33 _ dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-3 - [2-(3 -F1u0r0azetidiny1)pyridinyl] rnethy1—5 - [4- (trifluorornethyl)phenyl] -6,7-dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; 4- {(7S)-5 -[3 -Ch10ro(triflu0rornethyl)pheny1]rnethy1—4-ox0-4,5 ,6,7- tetrahydropyrazolo[ 1 ,5 -a]pyrazin-3 -yl} ethylarnino)pyridinecarbonitrile; (7S)-3 -(2-Azetidiny1pyridinyl)-5 - [3 -ch10r0(trifluor0rnethyl)phenyl] methyl-6,7-dihydr0pyrazolo[1 ,5-a]pyrazin-4(5H)—0ne; (7S)-3 -(2-Azetidiny1pyridinyl)-5 -(3 ,4-dichlorophenyl)—7-methy1—6,7 - dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [3 -(F1uorornethyl)(triflu0romethyl)phenyl]rnethyl-3 -(2-rnethy1pyridin-4 - y1)-6 ,7-dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl[4-(triflu0rornethyl)pheny1]-3 - [2-(trifluorornethyl)pyridiny1] -6,7- opyrazolo[1 ,5 -a]pyrazin-4(5H)-one; 4- {(7S)-5 -[3 o(triflu0rornethyl)pheny1]rnethy1—4-ox0-4,5 ,6,7- tetrahydropyrazolo[ 1 ,5 -a]pyrazin-3 -y1}pyridinecarbonitrile; (7S)-3 - [2 -(3 -Hydr0xyazetidiny1)pyridiny1] rnethy1—5 -[4- (trifluorornethyl)phenyl] -6,7-dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)-3 etidiny1pyridinyl)rnethy1—5 -[4-(triflu0romethyl)phenyl] -6 ,7- opyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [3 0(triflu0r0rnethyl)phenyl] rnethy1—3 -[2-(methylarnino)pyridin yl] -6 ,7-dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [3 -Ch10r0(triflu0r0rnethyl)phenyl] -3 -(2-methoxypyridiny1)rnethyl- 6,7-dihydr0pyrazolo[1 5 -a]pyrazin-4(5H)-one; (7S)Methyl-3 -(2-pyrr01idin-1 -y1pyridinyl)-5 -[4-(trifluor0rnethyl)phenyl] -6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-3 - Acetylpiperaziny1)pyridiny1] rnethy1—5 -[4- (trifluorornethyl)phenyl] -6,7-dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl-3 -(2-piperidin-1 -y1pyridinyl)-5 - [4-(trifluoromethyl)phenyl] -6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl-3 -(2-rn0rpholiny1pyridinyl)-5 -[4-(trifluor0rnethyl)phenyl] -6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; 4-[(7 S)-5 -(3 ,4-Dichlor0pheny1)rnethyloxo-4,5 ,6,7-tetrahydropyrazolo[1,5 - a]pyrazin-3 -y1]pyridinecarb0nitrile; (7S)-5 -(3 ,4-Dichlor0phenyl)rnethyl-3 -[2-(methylamino)pyridiny1] -6,7 - dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 ,4-Dichlor0pheny1)-3 -[2-(1-hydr0xyethyl)pyridiny1]rnethy1—6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)[2-(F1u0r0rnethyl)pyridinyl]rnethy1—5-[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(2-rnethy1pyridinyl)-5 -[4-(2,2,2-trifluorornethylethyl)pheny1]— 6,7-dihydr0pyrazolo[1 ,5-a]pyrazin-4(5H)-one; (7S)(3,4-Dichlor0phenyl)[2-(difluorornethyl)pyridiny1]rnethyl-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; -(3,4-Dichlor0pheny1)—7-(fluor0rnethyl)-3 -(2-rnethylpyridinyl)-6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-0ne (78 or 7R); -(3,4-Dichlor0pheny1)—7-(fluor0rnethyl)-3 ethylpyridinyl)-6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-0ne (7R or 78); (7S)(3,4-Dichlor0phenyl)[2-(fluoromethyl)pyridiny1]rnethyl-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; -(3,4-Dichlor0pheny1)—7-(rnethoxymethyl)(2-rnethylpyridinyl)-6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)—0ne (78 or 7R); -(3,4-Dichlor0pheny1)—7-(rnethoxymethyl)(2-rnethylpyridinyl)-6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-0ne (7R or 78); 7-(Meth0xymethyl)(2-rnethylpyridinyl)[4-(trifluor0rnethyl)phenyl]-6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-0ne (7R or 78); 7-(Meth0xymethyl)(2-rnethylpyridinyl)[4-(trifluor0rnethyl)phenyl]-6,7- opyrazolo[1,5-a]pyrazin-4(5H)-0ne (78 or 7R); (7S)(2-Cyclopropylpyridinyl)(3,4-dichloropheny1)rnethyl-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)(2-Eth0xypyridinyl)rnethyl[4-(triflu0rornethyl)phenyl]-6,7- dihydropyrazolo[ 1 ,5 azin-4(5H)-one; (7S)(3,4-Dichlor0phenyl)rnethyl[2-(1-methylethyl)pyridiny1]-6,7- opyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)(3,4-Dichlor0phenyl)[2-(hydroxymethyl)pyridinyl]rnethyl-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl-3 -[2-(1 -rnethylethy1)pyridiny1] -5 -[4-(triflu0r0rnethyl)phenyl] -6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; 4-{(7S)Methyloxo[4-(triflu0r0rnethyl)phenyl]-4,5,6,7- ydropyrazolo[ 1 ,5 -a]pyrazin-3 -y1}pyridinecarbonitrile; (7S)-3 -[2-(1 -Hydr0xyethy1)pyridiny1] rnethy1-5 - [4-(trifluoromethyl)phenyl] -6,7- opyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7R)Ethy1—3-(2-rnethylpyridinyl)[4-(triflu0romethyl)phenyl]-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)Ethy1—3-(2-rnethylpyridinyl)[4-(trifluor0rnethyl)phenyl]-6,7- W0 2014/195311 _ 35 _ opyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-3 - [2-(Diflu0rornethyl)pyridiny1] rnethyl-5 -[4-(trifluor0rnethyl)phenyl] -6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-0ne; (7S)-5 - [3 , 5 -Difluor0(trifluoromethyl)phenyl] rnethy1—3 -(2-rnethylpyridinyl)- 6,7-dihydr0pyrazolo[1 5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 ,4-Dichlor0phenyl)-3 h0xypyridinyl)rnethyl-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 ,4-Dichlor0phenyl)-3 -(2-ethy1pyridiny1)rnethy1—6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-3 - [2-(Hydr0xymethyl)pyridiny1]rnethy1-5 - [4-(trifluoromethyl)phenyl] -6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(2-methy1pyridinyl)-5 - {4- [1 - (trifluoromethyl)cyc10pr0pyl]pheny1} -6,7-dihydr0pyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 hlor0pheny1)rnethy1—3 -[2-(1-methylethoxy)pyridinyl]-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; -Methyl-3 -[2-(1 -rnethylethoxy)pyridinyl] -5 -[4-(trifluor0rnethyl)phenyl] -6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(4-Br0rn0phenyl)rnethyl-3 -(2-rnethylpyridinyl)-6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl-3 -(2-methyloxidopyridiny1)—5 - [4-(triflu0r0rnethy1)phenyl]-6,7 - dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(4-tert-Buty1phenyl)—7-methy1-3 -(2-rnethylpyridinyl)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 ,4-Dichlor0phenyl)-3 ethoxypyridiny1)rnethy1—6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; -(3 hlorophenyl)(methoxymethyl)-3 -(2-rnethy1pyridinyl)-6 7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; 7-(Methoxymethyl)(2-rnethylpyridinyl)-5 - [4-(trifluoromethyl)phenyl] -6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-3 -(2-Meth0xyrnethylpyridinyl)rnethyl-5 -[4-(trifluorornethyl)phenyl] - hydr0pyrazolo[1 5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 ,4-Dichlor0phenyl)-3 -(2-rneth0xymethylpyridiny1)rnethy1—6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl-3 -[2-(methylamino)pyridiny1] -5 - [4-(trifluoromethyl)phenyl] -6,7 - dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [3 -( 1 -Hydr0xyethy1)phenyl] rnethy1—3 -(2-rnethylpyridiny1)-6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; WO 95311 (7S)-5 - [4 -( 1 -Hydr0xyethy1)phenyl] thy1—3 -(2-rnethylpyridiny1)-6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)(6-Methoxypyridin-3 -y1)rnethy1—5 -[4-(trifluor0rnethyl)phenyl] -6,7 - opyrazolo[1 ,5 -a]pyrazin-4(5H)-one; - {(7S)Methy1—4-ox0-5 - [4-(trifluoromethyl)phenyl] -4,5 ,6,7- tetrahydropyrazolo[ 1 ,5 -a]pyrazin-3 -y1}pyridinecarbonitrile; (7S)Methyl(2-rnethy1pyridinyl)-5 -[4-(trifluorornethoxy)phenyl] -6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl-5 -[3 -methy1(trifluorornethyl)pheny1]-3 -pyridinyl-6,7 - dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl-5 -[3 -(1 -rnethylethoxy)(trifluoromethyl)phenyl] -3 -(2-rnethylpyridin- 6,7-dihydr0pyrazolo[1 yrazin-4(5H)-one; -[(7 S)Methy10X0-3 -pyridinyl-6,7-dihydr0pyrazolo[1,5 -a]pyrazin-5 (4H)-y1] - 2-(trifluor0rnethyl)benzonitrile; (7S)-5 -(4-Cyclopropylphenyl)rnethy1—3 ethy1pyridinyl)-6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-3 -(2 ,6-Dimethylpyridiny1)rnethyl-5 - [3 -rnethy1—4-(triflu0r0rnethyl)phenyl] - 6,7-dihydr0pyrazolo[1 5 -a]pyrazin-4(5H)-one; (7S)-5 - [3 -(Methoxymethyl)(trifluoromethyl)phenyl] rnethy1—3 -(2-rnethy1pyridin- 4-y1)-6,7-dihydr0pyrazolo[1 ,5-a]pyrazin-4(5H)-one; (7S)-5 -(3 ,5 -Dichlor0phenyl)rnethyl-3 -(2-methylpyridinyl)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(2-rnethy1pyridinyl)-5 -[4-(2,2,2-triflu0r0ethoxy)phenyl] -6 ,7- opyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(4-Ch10r0rneth0xyphenyl)—7-methyl-3 -(2-rnethylpyridinyl)-6,7 - dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [4-(Difluorornethyl)phenyl] rnethy1—3 -(2-rnethylpyridinyl)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [4-Ch10r0-3 -(difluor0methoxy)phenyl] rnethy1—3 -(2-rnethylpyridinyl)- hydr0pyrazolo[1 5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 ,4-Dichlor0pheny1)-3 -(2-fluoropyridinyl)rnethyl-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methy1—3-(2-rnethy1pyridinyl)-5 -[4-(2,2,2-trifluoro methylethoxy)phenyl] -6 ,7-dihydr0pyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)-3 - [2-(Dirnethylarnino)pyridiny1] rnethy1-5 - [4-(trifluoromethyl)phenyl] -6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(2,4-Dichlor0phenyl)rnethyl-3 -(2-methylpyridinyl)-6,7- W0 2014/195311 dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [3 -Ch10r0(diflu0r0rnethoxy)phenyl]rnethy1—3 -(2-methylpyridiny1)- 6,7-dihydr0pyrazolo[1 ,5-a]pyrazin-4(5H)-one; (7S)-5 - [4-Ch10r0-3 uoromethoxy)phenyl] rnethy1—3 -(2-methylpyridinyl)- 6,7-dihydr0pyrazolo[1 ,5-a]pyrazin-4(5H)-one; (7S)-5 -(3 ,4-Dichlorophenyl)rnethy1—3 -(2-rnethy1oxidopyridiny1)—6,7- dihydropyrazolo[1 ,5 azin-4(5H)-one; 7,7-Dimethyl(2-rnethylpyridinyl)[4-(trifluoromethyl)phenyl] -6,7- opyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(4-Ch10r0rnethy1phenyl)rnethyl-3 -(2-methylpyridinyl)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)(2-Cyclopropylpyridinyl)methyl-5 -[4-(trifluoromethyl)phenyl] -6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [3 -Ch10ro(diflu0romethyl)phenyl] rnethy1—3 -(2-methylpyridinyl)-6,7- opyrazolo[1 ,5 -a]pyrazin-4(5H)-one; -Methyl(2-piperaziny1pyridinyl)—5 - [4-(trifluoromethyl)phenyl] -6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(6-piperazinylpyridin-3 -y1)-5 - [4-(trifluoromethyl)phenyl] -6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [3 -Ch10r0(triflu0r0rnethyl)phenyl] -3 -[2-(2-fluoroethoxy)pyridiny1] methyl-6,7-dihydr0pyrazolo[1 ,5-a]pyrazin-4(5H)—0ne; (7S)(4-Chlor0phenyl)rnethy1—3 -[2-(rnethy1arnino)pyridinyl]-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; -[(7 S)Methy1-3 - [2-(rnethylarnino)pyridiny1] -6,7-dihydropyrazolo [1 ,5 - a]pyrazin-5 (4H)-y1] (trifluorornethyl)benzonitrile; (7S)(2-Methoxypyridinyl)-5 - [3 -rneth0xy(triflu0rornethyl)pheny1]rnethy1— 6,7-dihydr0pyrazolo[1 ,5-a]pyrazin-4(5H)-one; 7-(Diflu0r0rnethyl)—3 -(2-rnethylpyridinyl)-5 -[4-(triflu0r0rnethyl)phenyl] -6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [3 -F1u0r0(triflu0romethyl)phenyl]methy1—3 ethylarnino)pyridin 7-dihydropyrazolo[1 ,5-a]pyrazin-4(5H)-one; (7S)-5 - [3 -Methoxy(triflu0romethyl)phenyl] rnethy1—3 -[2-(rnethy1arnino)pyridin- 4-y1]-6,7-dihydr0pyrazolo[1,5-a]pyrazin-4(5H)-one; -(3 ,4-Dichlor0phenyl)—7-(fluorornethyl)-3 -[2-(methylarnino)pyridinyl] -6,7- dihydropyrazolo[1 ,5-a]pyrazin-4(5H)-0ne (7R or 78); -(3 ,4-Dichlor0phenyl)—7-(fluorornethyl)-3 -[2-(methylarnino)pyridinyl] -6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-0ne (78 or 7R); (7S)Methyl(2-rnethy1pyridinyl)-5 -[5 -(trifluorornethyl)pyridiny1]-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(5 -Chlor0pyridinyl)rnethyl-3 -(2-methylpyridinyl)-6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [6-Ch10r0-5 uor0rnethyl)pyridinyl] rnethy1-3 -(2-rnethylpyridiny1)- 6,7-dihydr0pyrazolo[1 5 -a]pyrazin-4(5H)-one; (7S)-5 - [4-Ethoxy-5 -(trifluorornethyl)pyridiny1]rnethy1—3 -(2-methy1pyridin y1)-6 ,7-dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methylpyridiny1—5 - [5 -(trifluoromethy1)pyridiny1] -6,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(5 -Ethoxyfluoropyridiny1)rnethy1—3 -(2-rnethy1pyridinyl)-6,7- opyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(2-rnethy1pyridinyl)-5 -[6-methyl-5 -(trifluoromethyl)pyridin yl] -6 ,7-dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl(2-rnethy1pyridinyl)-5 -[4-methyl-5 -(trifluoromethyl)pyridin yl] -6 ,7-dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-3 -(2 ,6-Dimethylpyridiny1)rnethyl-5 - [5 -(trifluoromethyl)pyridiny1] -6 ,7- dihydropyrazolo[1 ,5 azin-4(5H)-one; (7S)-5 -(3 -Chlor0eth0xypyridiny1)rnethyl-3 -(2-rnethylpyridinyl)-6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(5 -Chlor0rnethylpyridinyl)rnethyl-3 -(2-rnethylpyridinyl)-6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-3 -(2-Fluoropyridiny1)rnethyl-5 - [5 -(trifluor0rnethyl)pyridinyl] -6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(4-Ch10r0-5 ylpyridin-Z-yl)rnethyl-3 -(2-rnethylpyridinyl)-6 ,7- dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [6-Ethoxy-3 -(trifluorornethyl)pyridiny1]rnethy1—3 -(2-methy1pyridin y1)-6 ,7-dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [6-Ethoxy-5 -(trifluorornethyl)pyridiny1]rnethy1—3 -(2-methy1pyridin y1)-6 ,7-dihydropyrazolo[1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(5 -Chlor0eth0xypyridiny1)rnethyl-3 -(2-rnethylpyridinyl)-6 ,7- dihydropyrazolo[1 ,5 azin-4(5H)-one; (7S)-5 -(5 ,6-Dichlor0pyridinyl)rnethy1—3 ethy1pyridinyl)-6 ,7- dihydropyrazolo[1 ,5 azin-4(5H)-one; (7S)-5 -(4 ,5 -Dichloropyridin-Z-yl)rnethyl-3 -(2-rnethy1pyridinyl)-6 ,7- dihydropyrazolo[1 ,5 azin-4(5H)-one; (7S)-5 - [4-Ch10r0-5 -(trifluor0rnethyl)pyridinyl] rnethy1-3 -(2-rnethylpyridiny1)- 6,7-dihydr0pyrazolo[1 ,5-a]pyrazin-4(5H)-one; (7S)-3 -(2,6-Dimethylpyridinyl)-5 - [6-ethoxy-5 -(trifluoromethyl)pyridiny1] methyl-6,7-dihydr0pyrazolo[1 ,5-a]pyrazin-4(5H)—0ne; (7S)-5 -(5 -Chlor0rnethoxypyridiny1)rnethyl-3 -(2-rnethylpyridinyl)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [6-Meth0xy-5 -(trifluorornethyl)pyridinyl]rnethy1—3 -(2-rnethylpyridin yl)-6,7-dihydropyrazolo[1 ,5-a]pyrazin-4(5H)-one; (7S)-5 - [6-Ethoxy-5 -(trifluorornethyl)pyridiny1]rnethy1—3 -pyridinyl-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)-3 etidin-1 -y1pyridinyl)-5 -[6-methoxy-5 -(trifluorornethyl)pyridiny1] - 7-rnethyl-6,7-dihydr0pyrazolo [1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl[2-(methylarnino)pyridiny1] -5 - [5 -(trifluor0methyl)pyridiny1]- 6,7-dihydr0pyrazolo[1 ,5-a]pyrazin-4(5H)-one; 3 -(2-Methylpyridinyl)-5 -[5 -(trifluoromethyl)pyridiny1]-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 - [4-Iodo-5 -(trifluoromethyl)pyridin-Z-yl]rnethy1—3 -(2-methylpyridinyl)- hydr0pyrazolo[1 ,5-a]pyrazin-4(5H)-one; (7S)(4-Ch10r0i0dopyridiny1)rnethyl-3 -(2-rnethylpyridinyl)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)Methyl[2-(rnethylarnino)oxid0pyridiny1]—5 -[4- (trifluorornethyl)phenyl]-6,7-dihydr0pyrazolo[ 1 ,5 azin-4(5H)-one; (7S)(2-Ch10r0pyridinyl)methyl[4-(trifluoromethyl)phenyl] -6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; 7-(1 -Hydroxyethyl)-3 -(2-rnethylpyridinyl)-5 - [4-(trifluoromethyl)phenyl] -6,7- opyrazolo[ 1 ,5 -a]pyrazin-4(5H)-0ne (1R or 1 S); 7-(1 -Hydroxyethyl)-3 -(2-rnethylpyridinyl)-5 - [4-(trifluoromethyl)phenyl] -6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-0ne (1 S or IR); (7S)-3 -(2-Chloropyridinyl)-5 -(3 ,4-dich10r0phenyl)—7-methy1-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; -(3 ,4-Dichlor0pheny1)—7-(hydr0xymethyl)—3 thylpyridiny1)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(4,5 -Dich10roi0d0pheny1)—7-rnethy1—3 -(2-methylpyridiny1)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)-5 -(3 ,4-Dichloroi0dophenyl)—7-methyl-3 -(2-methylpyridiny1)-6,7- dihydropyrazolo[ 1 ,5 azin-4(5H)-one; -(3 ,4-Dichlor0phenyl)—7-(fluorornethyl)-3 ethylpyridinyl)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; _ 40 _ (7S)(2-Br0rn0pyridinyl)methyl[4-(trifluorornethyl)phenyl]-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; -(3 ,4-Dichlor0phenyl)—3-(2-fluor0pyridiny1)(hydr0xymethyl)—6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)(2-Iodopyridinyl)rnethy1—5-[4-(trifluorornethyl)phenyl]-6,7- opyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; -(3 ,4-Dichlor0phenyl)—3-(2-fluor0pyridiny1)(hydr0xymethyl)—6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-0ne (78 or 7R); -(3 ,4-Dichlor0phenyl)—3-(2-fluor0pyridiny1)(hydr0xymethyl)—6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-0ne (7R or 78); (7S)[3 -Ch10r0(triflu0romethyl)phenyl](2-flu0ropyridinyl)rnethyl-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)[3 -Brorn0(trifluorornethyl)phenyl]rnethy1—3 -(2-rnethylpyridinyl)-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; -(4-Iodophenyl)rnethy1—3-(2-rnethylpyridinyl)-6,7-dihydr0pyrazolo[1,5- a]pyrazin-4(5H)-one; -(3 ,4-Dichloropheny1)—3-[2-(dirnethylamino)pyridinyl](hydr0xymethyl)—6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-0ne (78 or 7R); -(3 ,4-Dichloropheny1)—3-[2-(dirnethylamino)pyridinyl](hydr0xymethyl)—6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-0ne (7R or 78); -(3 hlorophenyl)(hydr0xymethyl)—3-[2-(rnethylarnino)pyridiny1]-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)(2-Ch10r0rnethoxypyridiny1)rnethy1[4-(trifluoromethyl)phenyl]- 6,7-dihydr0pyrazolo[1 yrazin-4(5H)-one; (7S)[6-(1-Acetylazetidiny1)pyridiny1]rnethy1—5-[4- (trifluorornethyl)phenyl]-6,7-dihydr0pyrazolo[ 1 ,5-a]pyrazin-4(5H)-one (7S)Methyl(2-rnethylpyridinyl){4-[(trifluorornethyl)sulfany1]phenyl}-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)[6-Methoxy(trifluoromethyl)pyridinyl]rnethyl[2- (methylamino)pyridiny1]-6,7-dihydr0pyrazolo[1 ,5-a]pyrazin-4(5H)-one; ethy1pyridinyl)(trifluor0rnethyl)[4-(triflu0r0rnethyl)phenyl]-6,7- dihydropyrazolo[ 1 ,5 -a]pyrazin-4(5H)-one; (7S)[3 -(hydr0Xymethyl)—4-(trifluor0rnethyl)phenyl]rnethy1—3-(2-rnethy1 pyridyl)—6,7-dihydr0pyrazolo[ 1 ,5 -a]pyrazin0ne; (7S)(2-rnethoxypyridyl)[6-rnethoxy-5 -(triflu0rornethyl)pyridyl]rnethy1- 6,7-dihydr0pyrazolo[1 ,5 -a]pyrazin0ne; (7S)methyl[2-rnethy1—6-(methylarnino)pyridyl][4- _ 41 _ (trifluoromethy1)pheny1]-6,7-dihydropyraz010[ 1 ,5 -a]pyrazin0ne; (7S)-3 - [2-rneth0xy(rnethy1arnino)pyridy1] rnethy1-5 -[4- (trifluoromethy1)pheny1]-6,7-dihydropyraz010[ 1 ,5 -a]pyrazin0ne; (7S)-3 - [2-fluoro(methy1amino)pyridy1] thy1-5 - [4-(triflu0r0methy1)pheny1]— hydropyraz010[1 5 -a]pyrazin0ne; -(2,4-dich10r0pheny1)—3 ethy1pyridy1)-6,7-dihydr0pyraz010 [1 5 azin one; (7S)-3 - [2-(dirnethy1amino)—4-pyridy1]-5 - [3 -(hydroxymethy1)-4 - (trifluoromethy1)pheny1]rnethy1-6 ,7-dihydropyraz010 [1 ,5 azinone; (7S)-3 irnethy1amino)—4-pyridy1]-5 - [3 -(flu0r0rnethy1)—4- (trifluoromethy1)pheny1]rnethy1-6 ,7-dihydropyraz010 [1 ,5 -a]pyrazinone; (7S)-3 -(2-flu0r0pyridy1)rnethy1-5 -[4-(trifluoromethy1)pheny1]-6 ,7- dihydropyraz010[ 1 ,5 -a]pyrazinone; (7S)-5 -(3 ,4-dich10r0pheny1)-3 -[2-(dirnethy1arnino)pyridy1] rnethy1-6 ,7- dihydropyraz010[ 1 ,5 -a]pyrazinone; (7S)-3 -[2-(dirnethy1amino)—4-pyridy1]-5 - [3 -(2-flu0roethoxy) (trifluoromethy1)pheny1]rnethy1-6 ,7-dihydropyraz010 [1 ,5 -a]pyrazinone; (7S)-3 - [2-(dirnethy1amino)—4-pyridy1]-5 - [6-rneth0xy-5 -(triflu0r0rnethy1)pyridy1] methyl-6,7-dihydr0pyraz010[1 ,5 -a]pyrazinone; (7S)methy1-3 - [2-(rnethy1amino)—4-pyridy1]-5 -[3 -rnethy1 (trifluoromethy1)pheny1]-6,7-dihydropyraz010[ 1 ,5 -a]pyrazin0ne; (7S)-5 - [3 -ch10r0(triflu0romethy1)pheny1]rnethy1-3 -(2-methyl0Xid0-pyridin iurn—4-y1)-6,7-dihydr0pyrazolo [1 5 -a]pyrazinone; (7S)-3 - [2 -[ethy1(rnethy1)amino] pyridy1] rnethy1-5 -[4-(trifluoromethy1)pheny1] - 6,7-dihydropyraz010[1 5 -a]pyrazin0ne; (7S)-5 - [3 -ch10r0(trifluorornethy1)pheny1]-3 -[2- [ethy1(rnethy1)amino] pyridy1] methyl-6,7-dihydr0pyraz010[1 ,5 -a]pyrazinone; (7S)-5 - [3 -ch10r0(trifluorornethy1)pheny1]-3 -[2-(ethy1arnino)pyridy1] thy1- 6,7-dihydropyraz010[1 5 -a]pyrazin0ne; (7S)-3 - [2-(ethy1arnino)—4-pyridy1]rnethy1-5 - [3 -rnethy1(trifluor0rnethy1)pheny1]- 6,7-dihydropyraz010[1 5 -a]pyrazin0ne; (7S)-5 -(3 ,4-dich10r0pheny1)-3 thy1arnino)pyridy1] rnethy1-6,7- dihydropyraz010[ 1 ,5 -a]pyrazinone; (7S)methy1-5 - [3 -rnethy1(triflu0rornethy1)pheny1]-3 -[2-(pr0py1arnino)—4- pyridy1]-6 ,7-dihydropyraz010[1 ,5 -a]pyrazin0ne; (7S)methy1-3 - [2-(propy1arnin0)pyridy1] -5 - [4-(triflu0r0rnethy1)pheny1]-6 ,7- dihydropyraz010[ 1 ,5 -a]pyrazinone; _ 42 _ (7S)-3 - [2-(azetidin- l -yl)pyridyl] methyl-5 -[3 -methyl oromethyl)phenyl] -6,7-dihydropyrazolo[ l ,5 -a]pyrazinone; (7S)-3 - [2-(isopropylamino)pyridyl] methyl-5 - [3 -methyl (trifluoromethyl)phenyl] -6,7-dihydropyrazolo[ l ,5 -a]pyrazinone; (7S)-3 - [2-(isopropylamino)pyridyl] methyl-5 - ifluoromethyl)phenyl] -6,7 - dihydropyrazolo[ l ,5 -a]pyrazinone; (7S)-5 - [3 -chloro(trifluoromethyl)phenyl] -3 -[2-(fluoromethyl)pyridyl] methyl- hydropyrazolo[ l 5 -a]pyrazinone; (7S)-5 - [3 -chloro(trifluoromethyl)phenyl] methyl-3 - [2-(propylamino)pyridyl] - 6,7-dihydropyrazolo[ l 5 -a]pyrazinone; (7S)-5 -(3 ,4-dichlorophenyl)methyl-3 ropylamino)pyridyl] -6,7- dihydropyrazolo[ l ,5 -a]pyrazinone; (7S)-5 - [3 -chloro(trifluoromethyl)phenyl] -3 -[2-(isopropylamino)pyridyl] -7 - methyl-6,7-dihydropyrazolo[ l ,5 -a]pyrazinone; (7S)-5 -(3 ,4-dichlorophenyl)-3 -[2-(isopropylamino)pyridyl]methyl-6,7 - dihydropyrazolo[ l ,5 -a]pyrazinone; and the pharmaceutically acceptable salts and solvates of such compounds.
In another embodiment, specific compounds ing to the invention include: (7S)\/lethyl(2-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- opyrazolo[ l ,5-a]pyrazin-4(5H)-one hydrochloride salt; -\/lethyl(2-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one sulfate salt; (7S)\/lethyl(2-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[l,5-a]pyrazin-4(5H)-one methane sulfonate salt; (7S)\/lethyl(2-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- opyrazolo[ l ,5-a]pyrazin-4(5H)-one maleate salt; (7S)\/lethyl(2-methylpyridinyl)[3-methyl(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one hydrochloride salt; (7S)(3,4-Dichlorophenyl)methyl(2-methylpyridinyl)-6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one hydrochloride salt; (7S)[3 -Methoxy(trifluoromethyl)phenyl]methyl(2-methylpyridinyl)- 6,7-dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one hydrochloride salt; (7S)(4-Chlorophenyl)methyl-3 -(2-methylpyridinyl)-6,7-dihydropyrazolo[ l ,5 - a]pyrazin-4(5H)-one hydrochloride salt; (7S)(3 -Chloroethoxyphenyl)methyl(2-methylpyridinyl)-6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one hydrochloride salt; _ 43 _ -(3 -Chlorornethoxyphenyl)—7-rnethyl(2-rnethylpyridinyl)—6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one hydrochloride salt; (7S)[2-(Methoxyrnethyl)pyridinyl]rnethyl[4-(trifluorornethyl)phenyl]-6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one hydrochloride salt; (7S)(3,4-Difluorophenyl)rnethyl(2-rnethylpyridinyl)-6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one hloride salt; (7S)-5 uorophenyl)—7-rnethyl-3 -(2-rnethylpyridinyl)-6,7-dihydropyrazolo [l ,5 - a]pyrazin-4(5H)-one hloride salt; (7S)(3 -Fluorornethoxyphenyl)rnethyl(2-rnethylpyridinyl)-6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one hloride salt; (7S)(4-Methoxyphenyl)rnethyl(2-rnethylpyridinyl)—6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one hydrochloride salt; (7S)rnethyl(2-rnethylpyridyl)[3 -(trifluorornethoxy)phenyl]-6,7- dihydropyrazolo[ l ,5-a]pyrazinone hydrochloride salt; (7S)(3-chloro-5 -fluoro-phenyl)rnethyl-3 -(2-rnethylpyridyl)-6,7- dihydropyrazolo[ l ,5-a]pyrazinone hloride salt; (7S)(4-isopropylphenyl)rnethyl(2-rnethylpyridyl)-6,7- dihydropyrazolo[ l yrazinone hydrochloride salt; (7S)rnethyl-3 -(2-rnethylpyridyl)-5 opylphenyl)-6,7-dihydropyrazolo[ l ,5 - a]pyrazinone hydrochloride salt; (7S)[3 -(difluorornethoxy)fluoro-phenyl]rnethyl(2-methylpyridyl)—6,7- dihydropyrazolo[ l ,5-a]pyrazinone hydrochloride salt; (7S)Methyl[3-(l -rnethylethoxy)phenyl](2-rnethylpyridinyl)—6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one hydrochloride salt; (7S)(4-Ethoxyphenyl)rnethyl(2-rnethylpyridinyl)—6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one hydrochloride salt; (7S)Methyl(2-piperidin- l -ylpyridinyl)-5 - [4-(trifluorornethyl)phenyl] -6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)—one hydrochloride salt; (7S)(2-Cyclopropylpyridinyl)—5-(3,4-dichlorophenyl)rnethyl-6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one hydrochloride salt; (7S)(3,4-Dichlorophenyl)-3 -(2-ethoxypyridinyl)rnethyl-6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one hydrochloride salt; (7S)(3,4-Dichlorophenyl)rnethyl[2-(l-rnethylethoxy)pyridinyl]-6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one hydrochloride salt; (7S)Methyl-3 -[2-(l -rnethylethoxy)pyridinyl] -5 -[4-(trifluorornethyl)phenyl] -6,7- dihydropyrazolo[ l ,5-a]pyrazin-4(5H)-one hydrochloride salt; (7S)(2-Cyclopropylpyridinyl)—7-rnethyl[4-(trifluorornethyl)phenyl]-6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-one hydrochloride salt; (7S)Methyl(2-piperazinylpyridinyl)-5 - [4-(trifluoromethyl)phenyl] -6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-one hydrochloride salt, and (7S)Methyl(2-methylpyridinyl)-5 - {4- [(trifiuoromethyl)sulfanyl]phenyl} -6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-one hydrochloride salt.
The names of the compounds of the present invention were generated according to the nomenclature rules agreed upon by the Chemical Abstracts Service (C.A.S.) using Advanced Chemical Development, Inc., software (ACD/Name product version .01 .0.14105, October 2006). In case of tautomeric forms, the name of the depicted tautomeric form of the ure was generated. However it should be clear that the other non-depicted tautomeric form is also included within the scope of the present ion.
Definitions The notation "C1_4alkyl" as used herein alone or as part of another group, defines a saturated, straight or ed, hydrocarbon l having, unless otherwise stated, from 1 to 4 carbon atoms, such as methyl, ethyl, yl, 1-methylethyl, butyl, 1-methyl-propyl, 2-methylpropyl, 1,1 -dimethylethyl and the like. The notation "-C1_4alkyl-OH" as used herein alone or as part of another group, refers to C1_4alkyl as defined before, tuted with one OH group at any ble carbon atom.
The notation "halogen" or "halo" as used herein alone or as part of another group, refers to fluoro, chloro, bromo or iodo, with fluoro or chloro being preferred.
The notation "mono- and polyhaloC1_4alkyl" as used herein alone or as part of another group, refers to C1_4alkyl as defined before, substituted with 1, 2, 3 or where possible with more halo atoms as defined .
The notation "C3_7cycloalkyl" as used herein refers to a saturated, cyclic hydrocarbon radical having from 3 to 7 carbon atoms, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl. A particular C3_7cycloalkyl group is cyclopropyl.
The N—oxide forms of the compounds according to Formula (I) are meant to comprise those compounds of Formula (I) wherein one or several nitrogen atoms are oxidized to the so called N—oxide, particularly those N—oxides n a en atom in a pyridinyl radical is oxidized. N-oxides can be formed following procedures known to the d person. The N—oxidation on may generally be carried out by reacting the starting material of Formula (I) with an appropriate organic or inorganic peroxide. Appropriate inorganic peroxides comprise, for example, en peroxide, WO 95311 alkali metal or alkaline metal peroxides, e.g. sodium peroxide, potassium peroxide/ appropriate organic peroxides may comprise peroxy acids such as, for example, benzenecarboperoxoic acid or halo substituted benzenecarboperoxoic acid, e. g. 3-chloroperoxybenzoic acid (or 3-chloroperbenzoic acid), peroxoalkanoic acids, e. g. acetic acid, ydroperoxides, e.g. tert-butyl hydroperoxide. Suitable solvents, e. g are for example, water, lower alkanols, e. g. ethanol and the like, hydrocarbons, e.g. toluene, ketones, e.g. 2-butanone, halogenated hydrocarbons, e.g. dichloromethane, and mixtures of such solvents.
In a particular embodiment, the invention relates to a nd of Formula (I) wherein R5 K16) R6 R2 is and the rest of variables are as defined herein.
Whenever the term "substituted" is used in the present invention, it is meant, unless otherwise is indicated or is clear from the t, to indicate that one or more hydrogens, preferably from 1 to 3 hydrogens, more preferably from 1 to 2 hydrogens, more preferably 1 hydrogen, on the atom or radical indicated in the sion using "substituted" are replaced with a selection from the indicated group, provided that the normal valency is not exceeded, and that the substitution results in a chemically stable compound, i.e. a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into a therapeutic agent.
The term "subj ect" as used herein, refers to an animal, preferably a mammal, most preferably a human, who is or has been the object of treatment, observation or experiment.
The term peutically effective amount" as used herein, means that amount of active compound or pharmaceutical agent that elicits the biological or medicinal se in a tissue system, animal or human that is being sought by a researcher, veterinarian, medical doctor or other clinician, which includes alleviation of the symptoms of the disease or disorder being treated.
As used herein, the term "composition" is intended to encompass a product sing the specified ingredients in the specified amounts, as well as any product which results, directly or indirectly, from combinations of the specified ients in the specified amounts.
It will be appreciated that some of the compounds of Formula (I) and their pharmaceutically acceptable on salts and es thereofmay contain one or more centres of chirality and exist as stereoisomeric forms.
The term "compounds of the invention" as used herein, is meant to include the compounds of Formula (I), and the salts and solvates thereof.
As used herein, any chemical a with bonds shown only as solid lines and not as solid wedged or hashed wedged bonds, or otherwise ted as having a particular configuration (e. g. R, S) around one or more atoms, contemplates each possible stereoisomer, or mixture of two or more isomers.
Hereinbefore and hereinafter, the term "compound of a (1)" is meant to include the stereoisomers thereof and the tautomeric forms thereof.
The terms "stereoisomers", "stereoisomeric forms" or "stereochemically isomeric forms" hereinbefore or after are used interchangeably.
The invention includes all stereoisomers of the compounds of the invention either as a pure stereoisomer or as a mixture of two or more stereoisomers.
Enantiomers are stereoisomers that are non-superimposable mirror images of each other. A 1:1 mixture of a pair of enantiomers is a te or racemic mixture.
Diastereomers (or diastereoisomers) are stereoisomers that are not enantiomers, i.e. they are not related as mirror images. If a compound contains a double bond, the substituents may be in the E or the Z configuration. tuents on bivalent cyclic (partially) saturated radicals may have either the cis- or trans-configuration; for example if a compound contains a disubstituted cycloalkyl group, the substituents may be in the cis or trans configuration.
Therefore, the invention includes omers, diastereomers, racemates, E isomers, Z isomers, cis isomers, trans isomers and mixtures thereof, whenever ally possible.
The meaning of all those terms, i.e. enantiomers, diastereomers, racemates, E isomers, Z isomers, cis isomers, trans isomers and mixtures f are known to the skilled person.
The absolute configuration is specified according to the Cahn-Ingold-Prelog system. The configuration at an asymmetric atom is specified by either R or S.
Resolved stereoisomers whose absolute ration is not known can be designated by (+) or (-) depending on the direction in which they rotate plane polarized light. For instance, resolved enantiomers whose absolute configuration is not known can be designated by (+) or (-) depending on the direction in which they rotate plane polarized light.
When a specific isomer is fied, this means that said stereoisomer is substantially free, i.e. associated with less than 50%, ably less than 20%, more preferably less than 10%, even more preferably less than 5%, in particular less than 2% and most preferably less than 1%, of the other isomers. Thus, when a compound of 2014/061478 Formula (I) is for instance specified as (R), this means that the compound is substantially free of the (S) isomer; when a compound of Formula (I) is for instance specified as E, this means that the compound is substantially free of the Z isomer; when a compound of Formula (I) is for ce specified as cis, this means that the compound is substantially free of the trans isomer.
Some of the compounds according to a (I) may also exist in their tautomeric form. Such forms in so far as they may exist, although not explicitly indicated in the above formula are intended to be included within the scope of the present invention.
It follows that a single compound may exist in both stereisomeric and eric forms.
For therapeutic use, salts of the compounds of Formula (I) are those wherein the counterion is pharmaceutically acceptable. However, salts of acids and bases which are non-pharmaceutically acceptable may also find use, for e, in the preparation or purification of a pharmaceutically acceptable compound. All salts, whether pharmaceutically acceptable or not, are included within the ambit of the present invention.
The pharmaceutically acceptable acid and base addition salts as mentioned hereinabove or hereinafter are meant to se the therapeutically active non-toxic acid and base on salt forms which the compounds of Formula (I) are able to form.
The pharmaceutically acceptable acid addition salts can conveniently be obtained by ng the base form with such appropriate acid. Appropriate acids comprise, for example, inorganic acids such as hydrohalic acids, e. g. hydrochloric or hydrobromic acid, SlllfilI'lC, nitric, phosphoric and the like acids; or organic acids such as, for example, acetic, propanoic, hydroxyacetic, lactic, pyruvic, oxalic (i.e. ethanedioic), malonic, succinic (i.e. butanedioic acid), maleic, filmaric, malic, tartaric, citric, methanesulfonic, ethanesulfonic, benzenesulfonic, enesulfonic, ic, salicylic, p-aminosalicylic, pamoic and the like acids. Conversely said salt forms can be ted by treatment with an appropriate base into the fiee base form.
The compounds of Formula (1) containing an acidic proton may also be converted into their non-toxic metal or amine addition salt forms by treatment with appropriate organic and inorganic bases. Appropriate base salt forms comprise, for example, the ammonium salts, the alkali and earth alkaline metal salts, e. g. the lithium, , potassium, magnesium, m salts and the like, salts with organic bases, e. g. primary, secondary and tertiary aliphatic and aromatic amines such as methylamine, ethylamine, propylamine, isopropylamine, the four mine isomers, dimethylamine, diethylamine, diethanolamine, dipropylamine, diisopropylamine, di-n-butylamine, pyrrolidine, piperidine, morpholine, trimethylamine, triethylamine, tripropylamine, quinuclidine, pyridine, quinoline and isoquinoline; the benzathine, N-methyl-D-glucamine, hydrabamine salts, and salts with amino acids such as, for example, arginine, lysine and the like. Conversely the salt form can be converted by treatment with acid into the free acid form.
The term solvate comprises the solvent on forms as well as the salts f, which the compounds of Formula (I) are able to form. Examples of such solvent addition forms are e. g. hydrates, alcoholates and the like.
In the framework of this application, an element, in particular when mentioned in relation to a compound according to Formula (1), comprises all isotopes and isotopic mixtures of this element, either naturally occurring or synthetically ed, either with natural abundance or in an ically enriched form, for example 2H.
Radiolabelled compounds of a (I) may comprise a radioactive isotope selected from the group of 3H, 11C, 14C, 18F, 122I, 123I, 125I, 1311, 75Br, 76Br, 77Br and 82Br.
Preferably, the radioactive isotope is selected from the group of 3H, 11C and 18F.
Preparation The compounds according to the ion can generally be prepared by a succession of steps, each of which is known to the skilled . In particular, the compounds can be prepared according to the following synthesis methods.
The general preparation of some l examples of the compounds of Formula (I) is described hereunder and in the c examples, and are lly prepared from starting materials which are either commercially available or prepared by standard synthetic processes commonly used by those skilled in the art. The following schemes are only meant to represent examples of the invention and are in no way meant to be a limit of the ion.
Alternatively, compounds of the present invention may also be prepared by analogous reaction protocols as described in the general schemes below, combined with standard synthetic processes commonly used by those skilled in the art of organic chemistry.
The compounds of Formula (I) may be synthesized in the form of c mixtures of enantiomers which can be separated from one another following art-known resolution procedures. The racemic compounds of Formula (I) may be ted into the corresponding reomeric salt forms by reaction with a suitable chiral acid. Said diastereomeric salt forms are subsequently separated, for example, by selective or fractional crystallization and the omers are liberated therefrom by alkali. An alternative manner of separating the enantiomeric forms of the compounds of Formula (1) involves liquid tography using a chiral stationary phase or chiral supercritical fluid chromatography (SFC). Said pure stereochemically isomeric forms may also be derived from the corresponding pure stereochemically isomeric forms of the appropriate starting materials, provided that the reaction occurs stereospecif1cally.
The absolute ration of compounds of the invention reported herein was determined by analysis of the racemic mixture by supercritical fluid chromatography (SFC) ed by SFC comparison of the separate enantiomer(s) which were obtained by asymmetric synthesis or by chiral separation of mixtures, followed by vibrational circular dichroism (VCD) analysis of the particular omer(s).
A. Preparation of the final compounds Experimental procedure 1 Final compounds according to Formula (I) can be prepared by a Goldberg coupling reaction of a compound of Formula (II) with an appropriate aryl halide of Formula (111) where X is halo, in particular bromo or iodo, according to conditions known to the skilled person. Such conditions include for e using a suitable (I) catalyst such as copper(I) , in the presence of a ligand, such as N,N- dimethylethylenediamine, in the presence of a base, such as inorganic carbonates, for example sodium carbonate 3) or potassium carbonate (K2C03), in a suitable solvent, such as toluene or a mixture of toluene and N,N—dimethylformamide (DMF), under suitable reaction conditions, such as at a convenient temperature, typically g between 100 0C and 140 0C, in particular 110 CC, for a period of time to ensure the tion of the reaction. A nd of Formula (111) can be obtained commercially or made according to procedures known in the art. In Reaction Scheme 1, all variables are defined as in Formula (1).
Reaction Scheme 1 0 R2 0 R2 1 R1\ HN / R X N / RN‘N/ —> / (Ill) RN‘N R3 R4 R3 R4 (H) (I) Experimental procedure 2 Alternatively, final compounds according to Formula (I) can be prepared by a Suzuki type coupling reaction of a compound of Formula (IVa) with a suitable boron s or a compound of Formula (IVb), wherein R781 and R8a may be each independently ed from H, C1_4alkyl or R7&1 and R8&1 are taken together to form for example a bivalent radical of formula —CH2CH2—, -CH2CH2CH2— or — 2C(CH3)2—, with a suitable heteroaryl halide or aryl halide tive in the ce of a palladium catalyst, according to reaction conditions known to the skilled person. Such reaction conditions include the use of a palladium catalyst, such as tetrakis(triphenylphosphine)palladium(0) or an alternative catalyst system prepared in situ from Pd(OAc)2 and PPhg, a suitable base, such as N32C03, K2C03, NaOAc, NaHC03 or K3PO4, and in a suitable solvent, such as l,4-dioxane, or a mixture of dimethoxyethane (DME) and water. Degassing the reaction mixture with an inert gas, such as N2 or argon, and heating the reaction e to high temperatures, such as reflux temperature under classical heating or microwave irradiation, in particular 80 CC, may enhance the reaction outcome. In Reaction Schemes 2a and 2b, all variables are defined as in Formula (1).
Reaction Scheme 2a 0 | O R2 RLNJng RLNM N\N/ _’ N\N/ R3 R4 R3 R4 (IVa) (I) Reaction Scheme 2b OR7aO\B’ORBa O R2 "ng —> RLNM N \ N/ N \ N/ R3 R4 R3 R4 (IVb) (I) The suitable boron species may be selected for e from a boronic acid or a te ester, which may be conveniently ented as a compound of Formula R2\ ORBa 6R7a (IIIa) (Illa) wherein R2 is as defined in Formula (1) herein and R7&1 and R8&1 may be each independently selected from H, C1_4alkyl or R781 and R8a are taken together to form for example a bivalent radical of formula —CH2CH2—, -CH2CH2CH2— or —C(CH3)2C(CH3)2—. A skilled person can envisage that the reaction under Reaction Scheme 2a can also be performed under similar conditions, when the compound of Formula (IVa) bears a bromo group in place of an iodo group. Such a on can be represented as in Reaction Scheme 2c, wherein the compound of Formula (IV), wherein R2&1 is halo, in ular bromo or iodo and all other variables are as defined in Formula (I), undergoes a Suzuki type coupling as described hereinbefore.
Reaction Scheme 2c 0 R28 0 R2 Rwlyg1 1 / —> RWlYg/ N\N N\N R3 R4 R3 R4 Ex erimental rocedure 3 Alternatively, final compounds according to Formula (I), wherein R2 is an optionally substituted 4-pyridinyl or 3-pyridinyl, hereby referred to as compounds of Formula (Ia) or Formula (Ib), respectively, can be prepared by a reaction of deprotection of a compound of Formula (Ia-1) or a compound of Formula (Ia-2) following art known procedures. A compound of Formula (Ia) or a nd Formula (1b) can be obtained by removal of the protecting group such as for example a Boc protecting group in the nd of Formula (Ia-l) or compound of Formula (Ia-2), in the presence of acidic media, such as trifluoroacetic acid, in an inert t such as dichloromethane (DCM), under suitable reaction conditions, such as at a ient temperature, typically rt, for a period of time to ensure the completion of the on.
In on Schemes 3a and 3b, all variables are defined as in Formula (I) and Rsa’ and R6a, include the residues indicated in the scope as R5 and R6 as well as their protected forms.
Reaction Scheme 3a Reaction Scheme 3b (la-2) (lb) Ex erimental rocedure 4 Alternatively, final compounds according to Formula (Ia) and Formula (1b) can be prepared by manipulation of a suitable precursor of Formula (Ib-l) and of Formula (lb-2) respectively, bearing one or more fianctional groups which can be converted to the residues R5 and R6 by means of simple ons known to the person skilled in the art, such as for example introduction of an l or an amine in presence of a base and a suitable solvent or acylation with an acyl chloride in the presence of a base and a suitable solvent or reduction for example by using a suitable reducing agent such as sodium borohydride, in a suitable solvent or by means of cross coupling reactions known to the person d in the art, such as for example the Suzuki reaction with a suitable boron species or the Stille on with a suitable tin species. In on Schemes 4a and 4b, all les are defined as in Formula (I) and R5b and R6b include the residues indicated in the scope as R5 and R6 as well as their possible precursors. The person skilled in the art will recognize that suitable reaction ions should be chosen for different R5b and R6b combinations, to avoid undesired side reactions.
Reaction Scheme 4a WO 95311 Reaction Scheme 4b Ex erimental rocedure 5 Alternatively, final compounds according to Formula (Ia) and Formula (1b) can be prepared respectively by a reaction of ation of a compound of Formula (Ic-l) and of Formula (Ic-2) wherein Y is N, CH or CR90 and one of RSC, R6°, R3°, R4°, R90 and R100 may be each independently selected from C1_4alkyl-OH or C1_3alkyl-CHO and herein referred to as a compound of Formula (Ic-l) and compound of Formula (Ic-2) respectively. A nd of Formula (Ic-l) or compound of Formula (Ic-2) can be treated in the presence of a fluorinating agent such as for example ®Deoxofluor ([Bis(2-methoxyethyl)amino]sulfur trifluoride) or (diethylamino)sulfi1r trifluoride in a suitable solvent such as, for example DCM, and ng the reaction mixture at rt. In Reaction s 5a and 5b, all les are defined as in Formula (I) and RSC, R6°, R30, and R40 include the residues indicated in the scope of Formula (I) as R5, R6, R3 ,R4 as well as their possible precursors, and R90 and Rloc, when present, include the residues indicated in the scope of Formula (I) as substituents in R1 as well as their possible precursors, wherein one of RSC, R6°, R", R", and R9° and R100 when present, is C1_4alkyl-OH or C1_3alkyl-CHO and in (111%)," n = 0—4.
Reaction Scheme 5a Reaction Scheme 5b Experimental procedure 6 Alternatively, final compounds according to Formula (Ia) and Formula (1b) can be prepared by manipulation of a suitable precursor of Formula (Id-l) or of Formula (Id-2) tively, n Y is N, CH or CRgd, bearing one or more fianctional groups, R", R", R9d and R1", which can be ted to the es R5, R6 and the substituents of R1 as defined in Formula (I) by means of simple reactions known to the person skilled in the art, such as for example by reduction of a double bond to the corresponding saturated form, for example by means of catalytic hydrogenation. In Reaction Schemes 6a and 6b, all variables are defined as in a (I) and R5d and R", include the residues indicated in the scope as R5, R6 as well as their possible precursors, and R9d and R10d when present include the substituents of R1 as well as their possible precursors. The person skilled in the art will recognize that suitable reaction conditions should be chosen for different R", R", R9d and R10d combinations to avoid undesired side reactions and in (RIOd)n, n = 0-4.
Reaction Scheme 6a Reaction Scheme 6b (R10d)n /\"\|Y R3 R4 Ex erimental rocedure 7 Alternatively, final compounds according to Formula (Id) can be prepared by means of an oxidation reaction of a compound of Formula (I) in the presence of an oxidant, such as for e 3-chloroperoxybenzoic acid and in a suitable solvent. In Reaction Scheme 7, all variables are defined as in Formula (I).
Reaction Scheme 7 Ex erimental rocedure 8 Alternatively, final compounds according to Formula (I) can be prepared by intramolecular ion ng from a compound of Formula (VI). Typically, amidation conditions can be applied, such as stirring the starting materials, dissolved in a le solvent, such as DMF, in the presence of a coupling agent, such as HATU aza- lH-benzotriazole- l -yl)-l , l ,3 ,3 -tetramethyluronium hexafiuorophosphate) and in the presence of a base, such as TEA (triethylamine). In Reaction Scheme 8, all variables are defined as in Formula (I).
WO 95311 Reaction Scheme 8 0 R2 0 R2 R1 HOM ’ _’ R\NJ%’ NWN\ N\ N N R3 R4 R3 R4 (VD (D mental ure 9 Alternatively, final compounds according to Formula (I) can be prepared in one pot starting from a compound of Formula (II). First, a reaction of nucleophilic substitution of a compound of Formula (II) with an appropriate (hetero)aryl halide of Formula (111) where X is halo in the presence of a base such as for example sodium hydride in a suitable solvent such as for example DMF, followed by an intramolecular peptide type coupling of compound of Formula (VI) applying typical peptide type coupling conditions. Typically, peptide coupling conditions can be applied, such as stirring the starting als, dissolved in a suitable solvent, such as DMF, in the presence of a peptide coupling agent, such as HATU and in the presence of a base, such as TEA. In Reaction Scheme 9, all variables are defined as in Formula (1). on Scheme 9 0 R2 0 R2 0 R2 HN / RlX HO / N / RN / R1 / 0") N RN / NH/Y R3 R4 R3 R4 R3 R4 (II) (VI) (0 Alternatively, final compounds according to Formula (I) can be prepared in one pot starting from a compound of a (II). First by a coupling reaction of a compound of Formula (II) with an appropriate heteroaryl halide of Formula (111) where X is halo in the presence of a ium catalyst, such as tetrakis(triphenylphosphine)palladium(0), in the presence of a ligand, such as 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene, in the presence of a base, such as CSQCOg and in a suitable solvent, such as l,4-dioxane, under suitable on conditions, such as at a convenient temperature, typically ranging between 100 0C and 140 0C, for a period of time to ensure the completion of the reaction, followed by an olecular peptide type coupling of compound of a (VI) applying typical peptide type coupling ions. Typically, peptide coupling conditions can be applied, such as stirring the starting materials, dissolved in a suitable solvent, such as WO 95311 DMF, in the presence of a peptide coupling agent, such as HATU and in the presence of a base, such as TEA. In Reaction Scheme 9, all variables are defined as in Formula (1).
B. Preparation of the intermediate compounds Experimental ure 10 Intermediate compound according to Formula (II) (Reaction Scheme lOa) can be prepared following art known procedures, such as by subjecting an intermediate compound of Formula (Va) to a Suzuki type ng reaction under conditions known to a skilled person. Such conditions include for example, reacting the intermediate compound of a (Va) with a suitable boron species, such as for example a boronic acid or a te ester, for e as described in Experimental procedure 2 before, in the presence of a ium catalyst, such as tetrakis(triphenylphosphine)palladium(0) or an alternative catalyst system prepared in situ from Pd(OAc)2 and PPhg, a suitable base, such as N32C03, K2C03, NaHC03 and K3PO4, and in a suitable solvent, such as l,4-dioxane, or a mixture ofDME and water.
Degassing the reaction mixture with an inert gas, such as N2 or argon, and heating the reaction mixture to high atures, such as reflux temperature, in particular 80 CC, may enhance the reaction outcome. In Reaction Scheme lOa, all variables are defined as in Formula (I).
Reaction Scheme 10a 0 0 | R2 HN / HN / / _’ / N N ‘N ‘N R3 R4 R3 R4 (Va) (II) A skilled person can envisage that the reaction under Reaction Scheme lOa can also be performed under similar conditions, when the compound of Formula (Va) bears a bromo group in place of a iodo group. Such a reaction can be represented as in Reaction Scheme 10b, wherein the nd of Formula (V), wherein R281 is halo, in particular bromo or iodo and all other variables are as defined in Formula (I), undergoes a Suzuki type coupling as described hereinbefore.
Reaction Scheme 10b 0 R28 0 R2 / ' / N N ‘N ‘N R3 R4 R3 R4 (V) (II) In particular aspect, the invention ore s to an ediate compound of Formula (V), wherein R2&1 is halo, in ular Br or I 0 R28 R3 R4 (V).
In a particular embodiment, the invention relates to an intermediate compound of Formula (V’), wherein R2&1 is halo, in particular, Br (referred to herein as compound (I-13a) or I (referred to herein as nd (I-13)) §r \N (V’).
Ex erimental rocedure 11 Intermediate compound of Formula (Va) or of Formula (V) can be ed by removal of the protecting group, for example a Boc group, in an intermediate of Formula (VIa) or of Formula (VIb), respectively, for example in the presence of acidic media, such as hydrochloric acid, in an inert solvent such as 1,4-dioxane or acetonitrile or ethyl acetate (EtOAc), under suitable reaction conditions, such as at a convenient temperature, such as from 15 to 80 0C, typically 80 0C or from 15-30 0C depending on the solvent system, for a period of time to ensure the completion of the reaction followed by treatment with a base such as N32C03, K2C03 or NaHCOg, under suitable reaction conditions, such as at a convenient temperature, typically ranging between 0 0C and 40 0C, in particular from 15 to 30 0C, for a period of time to ensure the completion of the reaction. In Reaction Schemes 11a and 11b, R2&1 is halo, in particular bromo or iodo, R7 is C1_4alkyl, PG is a ting group, for example Boc, and all other variables are defined as in Formula (I).
Reaction Scheme 1 la (Vla) (Va) Reaction Scheme llb 0 0 R23 R28 \0 / HN / / / N\ Kr"\ N N (Vlb) (V) Experimental procedure 12 Intermediate compound of Formula (VIa) or (VIb) wherein R7 is C1_4alkyl and PG is a protecting group, for example Boc, can be prepared by a Mitsunobu type reaction between an intermediate compound of Formula (VIIa) or (VII) respectively, and an appropriate l of Formula (VIII), in the presence of a suitable triarylphosphine, such as triphenylphosphine typically 15 equivalents, or a suitable trialkylphosphine, and a suitable dialkyl azodicarboxylate t, such as di-tert—butyl azodicarboxylate or l azodicarboxylate typically 15 equivalents, in a suitable inert solvent, such as tetrahydrofuran (THF), under suitable reaction conditions, such as at a convenient temperature, typically ranging 0 0C and rt, e.g. 20 CC, for a period of time to ensure the tion of the reaction. An intermediate compound of a (VIII) can be obtained commercially or synthesized according to literature procedures.
Intermediate compound of Formula (VIIa) wherein R7 is C1_4alkyl, can be ed via a reaction of halogenation of intermediate of Formula (IX) with a nating reagent such as N-iodosuccinimide, in an inert solvent such as dichloromethane, under suitable reaction conditions, such as at a convenient temperature, lly rt, for a period of time to ensure the completion of the reaction.
Intermediate compound of Formula (VII), wherein R7 is methyl and R2&1 is bromo, can be obtained commercially and is a ularly preferred material for use in the synthesis, including large scale, of a variety of final compounds of Formula (I) according to the l ures described herein. An intermediate compound of Formula (IX) can be obtained commercially or synthesized according to literature procedures. _ 60 _ In Reaction Scheme 12a and 12b, R2&1 is halo, in particular bromo or iodo, R7 is C1_4alkyl, PG is a protecting group, such as for example Boc, and all other variables are defined as in Formula (1).
Reaction Scheme 12a OH 0 I o o I PG-HN/W R1 R1 R7\ R3 R4 O / o / —> o / —> / HN\N/ HN\N/ ‘N (VIII) PG_HN/§< R3 R4 (IX) (Vlla) (Vla) Reaction Scheme 12b OH 0 R28 0 Rza Pam/7K4 R1 R7\ R R O / o / —> / HN\N/ (VIII) pG_HN/§< N R3 R4 (VII) (Vlb) Experimental procedure 13 Intermediate compound of Formula (IVb) can be prepared via a on of boronic ester or boronic acid formation starting from an intermediate of Formula (IVa) with a trans metallating agent such as for example BuLi or a Grignard reagent, a ular example of reagents includes isopropylmagnesium chloride lithium de complex solution and a boron species such as 2-z's0propoxy-4,4,5,5-tetramethyl-l,3,2- dioxaborolane, in an inert solvent such as ous THF, under suitable reaction conditions, such as at a convenient temperature, typically -25°C, for a period of time to ensure the completion of the reaction. Depending on reaction conditions, c ester or boronic acid are obtained. In Reaction Scheme 13, R7&1 and R881 are H or C1_4 alkyl or R7&1 and R881 are taken together to form for e a bivalent l of formula — CH2CH2—, -CH2CH2CH2— or —C(CH3)2C(CH3)2—, and all other variables are defined as in Formula (I).
Reaction Scheme 13 R7ao\ 8 O I o B’ORa R\1 NM N\ —> RWM1 R / N RN‘N R3 R4 R3 R4 Experimental procedure 14 Intermediate compound of Formula (IVa) can be prepared via a on of nation of an intermediate of Formula (X) with a nating reagent such as iodine, in the presence of ammonium cerium(IV) nitrate and in an inert solvent such as acetonitrile, under suitable reaction conditions, such as at a convenient temperature, typically 70 0C, for a period of time to ensure the completion of the reaction. In an analogous manner, intermediate compound of a (Va) can be prepared from intermediate of Formula (XI). In Reaction Schemes 14a and 14b, all variables are defined as in Formula (1).
Reaction Scheme 14a 0 o R‘NJ%1 R‘NM1 / —> / R3 R4 R3 R4 (X) (IVa) Reaction Scheme 14b 0 o I m)?»/ —> HNM/ N\N N\N R3 R4 R3 R4 (XI) (Va) Ex erimental re l5 Intermediate compound of Formula (X) can be ed by a coupling reaction of an intermediate compound of Formula (XI) with an appropriate aryl/heteroaryl halide of Formula (III) where X is halo with a le copper(I) catalyst such as copper(I) iodide, in the presence of a ligand, such as N,N-dimethylethylenediamine, in the presence of a base, such as N32C03, in a suitable solvent, such as toluene, under suitable reaction conditions, such as at a convenient temperature, typically ranging between 100 0C and 140 0C, for a period of time to ensure the completion of the reaction. In an analogous manner, intermediate nd of Formula (IV) can be ed from intermediate of Formula (V). An intermediate compound of Formula (III) can be obtained commercially. In Reaction Schemes 15a and 15b, all variables are defined as in Formula (I) and R2&1 is halo, in particular bromo or iodo.
WO 95311 _ 62 _ on Scheme 15a 0 o kKN‘N/ —> L7 / N‘N m0 N‘N R3 R4 R3 R4 (V) (IV) Ex erimental rocedure l6 Intermediate compound of Formula (XI) can be prepared by removal of the protecting group in an intermediate of Formula (XII), for example in the presence of acidic media, such as hydrochloric acid, in an inert solvent such as l,4-dioxane, under suitable reaction ions, such as at a convenient temperature, lly 80 0C, for a period of time to ensure the completion of the reaction followed by treatment with a base, such as Na2C03 or NaHCOg, under suitable reaction conditions, such as at a convenient ature, typically ranging between 0 0C and 40 0C, for a period of time to ensure the completion of the reaction. In an analogous manner, intermediate compound of Formula (V) can be prepared from intermediate of Formula (VIb). In Reaction Schemes 16a and 16b, R2&1 is halo, in particular bromo or iodo, R7 is C1_4alkyl, PG is a protecting group and all other variables are defined as in Formula (I).
Reaction Scheme 16a 0 O / —> / N\ N PG—HN/K 4 N R R R (XII) (XI) Reaction Scheme 16b 0 0 R23 R28 \0 / HN / (Vlb) (V) Experimental procedure 17 Intermediate compound of a (XII) n R7 is C1_4alkyl and PG is a protecting group, can be prepared by a Mitsunobu type reaction between a compound of Formula (IX) and an appropriate alcohol of Formula (VIII), in the presence of a suitable triarylphosphine, such as triphenylphosphine, or a suitable ylphosphine, and a suitable dialkyl azodicarboxylate reagent, such as di-tert—butyl azodicarboxylate, in a suitable inert solvent, such as THF, under suitable reaction conditions, such as at a convenient temperature, typically rt, for a period of time to ensure the completion of the reaction. Intermediate compounds of Formula (IX) and of Formula (VIII) can be obtained commercially or synthesized according to literature ures. In Reaction Scheme 17, R7 is C1_4alkyl, PG is a protecting group and all other variables are defined as in Formula (I).
Reaction Scheme 17 OH o o PG—HN/X R7 R7\O)S/> R3 R4 \0 / / / HN\N/ (VIII) PG_HN/§< N R3 R4 (IX) (XII) Experimental procedure 18 Intermediate compound of Formula (IX) wherein R7 is C1_4alkyl can be ed by esterification of the commercially ble intermediate compound of Formula (XIII), by methods known to the person skilled in the art, or may be commercially available. The reaction can be performed for example in the presence of an acidic agent, such as sulfiIric acid, and an alcohol, such as EtOH, in a le solvent, such as EtOH, under suitable on conditions, such as at a convenient temperature, typically between 80 0C and 100 0C, for a period of time to ensure the completion of the reaction.
In Reaction Scheme 18, R7 is C1_4alkyl.
Reaction Scheme 18 o 0 HN\N/ R7\0J\é> H \N’ (XIII) (IX) Experimental procedure 19 Intermediate nd of Formula (XI) wherein R3 is H and R4 is CF3 herein referred to as compounds of Formula (XIa) can be prepared by hydrogenation of an intermediate of Formula (XIV) followed by one pot intramolecular cyclization, in the presence of a hydrogenation catalyst, such as Pd/C (palladium on ), under hydrogen atmosphere generated by using ammonium formate, in an inert t such as MeOH, under suitable reaction conditions, such as at a convenient temperature, typically 70 0C, for a period of time to ensure the completion of the reaction. In Reaction Scheme 19, R7 is C1_4alkyl.
Reaction Scheme 19 O 0 O / HN / N‘N/ —’ Kr" / oZN/Y ‘N CF3 CF3 (XIV) (XIa) Ex erimental re 20 Intermediate compound of Formula (XIV) wherein R7 is C1_4alkyl, can be prepared by an intermolecular reaction between an appropriate hydrazine of Formula (XV), in the presence of a suitable ter of a (XVI), such as ethyl te, in a suitable inert solvent, such as EtOH, under suitable reaction conditions, such as at a convenient temperature, typically rt, for a period of time to ensure the completion of the on. Intermediate compound of Formula (XVI) can be obtained commercially or synthesized according to literature procedures. In Reaction Scheme 20, R7 is C1- 4alkyl.
Reaction Scheme 20 R:OAK)?O 'T'HZ (XVI) R1 NH 0 ()sz , // 3 OgN/YN\N (XV) (XIV) Ex erimental rocedure 21 Intermediate compound of Formula (XV) can be prepared by a reaction of deprotection of a compound of Formula (XVI) following art known ures. A compound of a (XV) can be obtained by removal of the protecting group such as for example a Boc protecting group in the compound of Formula (XVI), in the presence of acidic media, such as hydrochloric acid, in an inert solvent such as MeOH, under suitable reaction conditions, such as at a convenient temperature, typically rt, for a period of time to ensure the tion of the reaction.
Intermediate compound of Formula (XVI) can be obtained by addition of a protected hydrazine of Formula (XVIII) to 3,3,3-trifluoro-l-nitro-prop-l-ene (XVII) (prepared as described in J. Fluorine Chem. 2008, 767-774). In Reaction Scheme 21, PG is a protecting group, for example BOC.
Reaction Scheme 21 (XVIII) 0 "N HN’PG NH2 2 OZN/E;NH ' NH —’ CF3 OzN/Y CF3 3 (XVII) (XVI) (XV) In order to obtain the HCl salt forms of the compounds, l procedures known to those skilled in the art can be used. In a typical procedure, for example, the free base can be ved in DIPE or EtzO and subsequently, a 6N HCl solution in 2-propanol, 4N HCl solution in dioxane, or a 1N HCl solution in EtzO can be added dropwise. The mixture lly is d for 10 minutes after which the product can be filtered off.
The HCl salt usually is dried in vacuo.
It will be appreciated by those skilled in the art that in the processes described above the fianctional groups of intermediate compounds may need to be blocked by protecting groups. In case the functional groups of intermediate compounds were blocked by protecting groups, they can be deprotected after a reaction step.
Pharmacology The compounds provided in this invention are negative allosteric modulators (NAMs) of metabotropic glutamate receptors, in particular they are negative allosteric modulators of mGluR2. The compounds of the present ion do not appear to bind to the glutamate recognition site, the orthosteric ligand site, but instead to an eric site within the seven transmembrane region of the receptor. In the presence of ate, the compounds of this invention decrease the mGluR2 se. The compounds provided in this invention are expected to have their effect at mGluR2 by virtue of their y to decrease the response of such receptors to glutamate, ating the response of the receptor.
As used herein, the term "treatment" is intended to refer to all processes, wherein there may be a slowing, interrupting, arresting or stopping of the progression of a disease or an alleviation of symptoms, but does not necessarily indicate a total elimination of all ms.
Hence, the present invention s to a compound according to the general Formula (I), or a isomeric form thereof, or an N—oxide thereof, or a pharmaceutically acceptable salt or a solvate thereof, in particular, a compound of Formula (I) or a stereoisomeric form thereof, or a pharmaceutically able salt or a solvate thereof for use as a medicament.
The invention also s to the use of a compound according to the general Formula (I), or a stereoisomeric form thereof, or an N—oxide thereof, or a pharmaceutically acceptable salt or a solvate thereof, in particular, a compound of Formula (I) or a stereoisomeric form thereof, or a ceutically acceptable salt or a solvate thereof, or a pharmaceutical composition according to the invention for the manufacture of a medicament.
The invention also relates to a compound according to the general Formula (I), or a stereoisomeric form thereof, or an N—oxide thereof, or a ceutically able salt or a solvate thereof, in particular, a compound of Formula (I) or a stereoisomeric form thereof, or a pharmaceutically acceptable salt or a solvate thereof, or a pharmaceutical composition according to the invention for use in the treatment or prevention of, in particular treatment of, a condition in a mammal, including a human, the treatment or tion of which is affected or facilitated by the neuromodulatory 2014/061478 effect of allosteric modulators of mGluR2, in particular negative allosteric modulators thereof.
The present invention also relates to the use of a compound according to the general Formula (I), or a stereoisomeric form thereof, or an N—oxide thereof, or a pharmaceutically acceptable salt or a solvate thereof, in particular, a compound of Formula (I) or a stereoisomeric form thereof, or a pharmaceutically acceptable salt or a solvate thereof, or a pharmaceutical ition according to the invention for the manufacture of a medicament for the treatment or prevention of, in particular treatment of, a condition in a mammal, including a human, the treatment or prevention of which is ed or facilitated by the neuromodulatory effect of allosteric modulators of mGluR2, in particular negative allosteric modulators thereof The present invention also s to a compound according to the general a (I), or a stereoisomeric form thereof, or an N—oxide thereof, or a pharmaceutically acceptable salt or a solvate thereof, in particular, a compound of a (I) or a stereoisomeric form thereof, or a pharmaceutically acceptable salt or a solvate thereof, or a pharmaceutical composition according to the invention for use in the treatment, prevention, amelioration, control or reduction of the risk of various neurological and atric disorders associated with ate dysfunction in a mammal, including a human, the treatment or prevention of which is affected or facilitated by the neuromodulatory effect of negative allosteric modulators of mGluR2.
Also, the present invention relates to the use of a nd according to the general Formula (I), or a stereoisomeric form thereof, or an e thereof, or a pharmaceutically able salt or a solvate thereof, in particular, a compound of Formula (I) or a stereoisomeric form thereof, or a pharmaceutically acceptable salt or a solvate thereof, or a pharmaceutical composition according to the invention for the manufacture of a medicament for treating, preventing, ameliorating, controlling or reducing the risk of various neurological and psychiatric disorders associated with glutamate dysfunction in a mammal, including a human, the ent or prevention of which is affected or facilitated by the neuromodulatory effect of negative allosteric modulators ofmGluR2.
In ular, the neurological and psychiatric ers associated with glutamate dysfunction, include one or more of the following l nervous system conditions or es: mood disorders; delirium, dementia, amnestic and other cognitive disorders; disorders y first diagnosed in infancy, childhood or adolescence; substance-related ers; schizophrenia and other psychotic disorders; somatoform disorders; and hypersomnic sleep disorder.
In particular, the central nervous system disorder is a tic er selected from the group of phrenia (in particular in antipsychotic-stabilized patients), schizophreniform disorder, schizoaffective disorder, onal disorder, brief psychotic disorder, and substance-induced psychotic er.
In particular, the central nervous system disorder is a substance-related disorder selected from the group of alcohol dependence, alcohol abuse, amphetamine ence, amphetamine abuse, caffeine dependence, caffeine abuse, cannabis ence, cannabis abuse, cocaine dependence, cocaine abuse, hallucinogen dependence, hallucinogen abuse, nicotine dependence, nicotine abuse, opioid dependence, opioid abuse, phencyclidine dependence, and phencyclidine abuse.
In particular, the l nervous system disorder is a mood disorder selected from the group of major depressive disorder, depression, treatment ant depression, dysthymic er, cyclothymic disorder, and substance-induced mood disorder.
In ular, the central nervous system disorder is a disorder usually first diagnosed in infancy, childhood, or adolescence selected from mental retardation, learning disorder, motor skills disorder, communication disorder, attention-deficit and disruptive behaviour disorders (such as Attention-Def1cit/Hyperactivity Disorder (ADHD)). An additional disorder usually first diagnosed in infancy, childhood, or adolescence is autistic disorder.
In particular, the central s system disorder is a cognitive disorder selected from the group of dementia, in particular, dementia of the Alzheimer’s type, vascular dementia, dementia due to HIV disease, dementia due to head trauma, dementia due to son’s disease, dementia due to Huntington’s disease, dementia due to Pick’s disease, dementia due to feldt-Jakob disease, and substance-induced persisting dementia.
In ular, the central nervous system disorder is an amnestic disorder, such as substance-induced persisting amnestic disorder.
As already mentioned hereinabove, the term "treatment" does not necessarily indicate a total elimination of all symptoms, but may also refer to symptomatic treatment in any of the disorders mentioned above. In particular, symptoms that may be treated include but are not limited to, memory impairment in particular in dementia or in major depressive er, age-related cognitive decline, mild cognitive impairment, and depressive symptoms.
Ofthe disorders mentioned above, the treatment of dementia, major depressive disorder, depression, treatment resistant depression, ion-deficit/hyperactivity disorder and phrenia, in particular in antipsychotic-stabilized patients, are of particular importance.
The fourth edition of the Diagnostic & Statistical Manual of Mental Disorders (DSM-IV) of the American Psychiatric Association provides a diagnostic tool for the identification of the disorders described herein. The person skilled in the art will recognize that alternative nomenclatures, nosologies, and fication systems for neurological and psychiatric disorders described herein exist, and that these evolve with medical and scientific progresses.
A skilled person will be familiar with alternative nomenclatures, nosologies, and classification systems for the diseases or conditions referred to herein. For example, the "American Psychiatric Association: stic and Statistical Manual of Mental Disorders, Fifth Edition. Arlington, VA, American Psychiatric ation, 2013" (DSM-STM) es terms such as sive disorders, in particular, major depressive disorder, persistent sive disorder (dysthymia), substance-medication-induced depressive disorder; neurocognitive disorders (NCDs) (both major and mild), in particular, neurocognitive disorders due to Alzheimer’s e, vascular NCD (such as vascular NCD present with multiple infarctions), NCD due to HIV infection, NCD due to traumatic brain injury (TBI), NCD due to Parkinson’s disease, NCD due to Huntington’s disease, frontotemporal NCD, NCD due to prion disease, and substance/medication-induced NCD; neurodevelopmental disorders, in particular, intellectual disability, specific learning disorder, neurodevelopmental motor disorder, communication disorder, and attention-deficit/hyperactivity disorder (ADHD); substance-related disorders and addictive disorders, in ular, alcohol use disorder, amphetamine use disorder, cannabis use disorder, e use disorder, other hallucinogen use disorder, tobacco use er, opiod use disorder, and clidine use disorder; schizophrenia spectrum and other psychotic disorders, in particular, schizophrenia, schizophreniform er, schizoaffective er, delusional er, brief psychotic disorder, substance/medication-induced psychotic disorder; somatic symptom disorders; hypersomnolence disorder; and cyclothymic disorder (which under DSM-STM falls under the bipolar and related disorders category). Such terms may be used by the skilled person as an alternative nomenclature for some of the diseases or conditions referred to herein. An additional neurodevelopmental er includes autism spectrum er (ASD), which encompasses according to the DSM-STM, disorders usly known by the terms early infantile autism, childhood autism, Kanner’s autism, high-fianctioning autism, atypical autism, pervasive developmental disorder not otherwise specified, childhood disintegrative disorder, and Asperger’s disorder. In ular, the disorder is autism. Specifiers associated with ASD include those Where the individual has a genetic disorder, such as in Rett syndrome or Fragile X syndrome.
Therefore, the invention also relates to a nd ing to the l Formula (I), or a stereoisomeric form thereof, or an N—oxide thereof, or a pharmaceutically acceptable salt or a solvate thereof, in ular, a compound of a (I) or a stereoisomeric form thereof, or a pharmaceutically able salt or a solvate thereof, for use in the treatment of any one of the diseases mentioned hereinbefore.
The invention also relates to a compound according to the general Formula (I), or a isomeric form thereof, or an N—oxide thereof, or a pharmaceutically acceptable salt or a solvate thereof, in particular, a compound of Formula (I) or a stereoisomeric form thereof, or a pharmaceutically acceptable salt or a solvate f, for use in treating any one of the diseases mentioned hereinbefore.
The invention also relates to a compound ing to the general Formula (I), or a stereoisomeric form thereof, or an N—oxide thereof, or a pharmaceutically acceptable salt or a solvate thereof, in particular, a compound of Formula (I) or a stereoisomeric form thereof, or a pharmaceutically acceptable salt or a e thereof, for the treatment or prevention, in particular ent, of any one of the diseases mentioned hereinbefore.
The ion also relates to the use of a compound according to the general a (I), or a stereoisomeric form thereof, or an N—oxide thereof, or a pharmaceutically acceptable salt or a solvate thereof, in particular, a compound of Formula (I) or a stereoisomeric form thereof, or a pharmaceutically acceptable salt or a solvate thereof, for the manufacture of a medicament for the treatment or prevention of any one of the disease conditions mentioned hereinbefore.
The compounds of the present ion can be administered to s, preferably humans, for the treatment or prevention of any one of the es mentioned hereinbefore.
In View of the utility of the compounds of Formula (I), there is provided a method of treating warm-blooded animals, including humans, suffering from any one of the diseases mentioned hereinbefore, and a method of preventing in warm-blooded animals, including humans, any one of the diseases mentioned hereinbefore.
Said methods comprise the administration, i.e. the systemic or topical administration, preferably oral administration, of a therapeutically effective amount of a compound of Formula (I), a stereoisomeric form thereof, or an N-oxide thereof, or a pharmaceutically acceptable salt or solvate thereof, in particular, a compound of Formula (I) or a stereoisomeric form thereof, or a pharmaceutically acceptable salt or a solvate f, to warm-blooded animals, including humans.
Therefore, the invention also relates to a method for the tion and/or treatment of any one of the diseases ned hereinbefore comprising administering a therapeutically effective amount of a compound according to the invention to a subject in need thereof.
One skilled in the art will recognize that a therapeutically effective amount of the NAMs of the present invention is the amount sufficient to modulate the activity of the mGluR2 and that this amount varies inter alia, depending on the type of disease, the tration of the compound in the therapeutic formulation, and the ion of the patient. lly, an amount ofNAM to be administered as a therapeutic agent for treating diseases in which modulation of the mGluR2 is beneficial, such as the disorders described , will be determined on a case by case by an attending physician.
Generally, a suitable dose is one that results in a concentration of the NAM at the treatment site in the range of 0.5 nM to 200 uM, and more usually 5 nM to 50 uM.
To obtain these treatment trations, a patient in need of treatment likely will be administered an effective therapeutic daily amount of about 0.01 mg/kg to about 50 mg/kg body weight, preferably from about 0.01 mg/kg to about 25 mg/kg body weight, more preferably from about 0.01 mg/kg to about 10 mg/kg body , more preferably from about 0.01 mg/kg to about 2.5 mg/kg body weight, even more preferably from about 0.05 mg/kg to about 1 mg/kg body weight, more preferably from about 0.1 to about 0.5 mg/kg body weight. The amount of a compound ing to the present invention, also referred to here as the active ingredient, which is required to achieve a therapeutically effect will, of course vary on case-by-case basis, vary with the particular compound, the route of administration, the age and condition of the recipient, and the particular disorder or disease being treated. A method of ent may also include administering the active ingredient on a n of between one and four intakes per day. In these methods of treatment the compounds according to the invention are preferably formulated prior to admission. As described herein below, le pharmaceutical formulations are prepared by known procedures using well known and readily available ingredients.
WO 95311 The compounds of the present invention may be utilized in combination with one or more other drugs in the treatment, prevention, control, amelioration, or reduction of risk of diseases or conditions for which nds of Formula (I) or the other drugs may have utility, where the combination of the drugs together are safer or more effective than either drug alone. Examples of such combinations include the compounds of the ion in combination with antipsychotic(s), NMDA receptor antagonists (e. g. memantine), NR2B antagonists, acetylcholinesterase inhibitors (e. g. donepezil, galantamine, physostigmine and igmine) and/or antidepressant ransmitter reuptake inhibitors. Particular combinations include the compounds of the invention in combination with antipsychotics, or the compounds of the ion in combination with memantine and/or NRZB antagonists.
Pharmaceutical compositions The present invention also provides compositions for preventing or ng diseases in which tion of the mGluR2 receptor is beneficial, such as the disorders described . While it is possible for the active ingredient to be administered alone, it is preferable to present it as a pharmaceutical composition.
Accordingly, the present invention also relates to a pharmaceutical composition comprising a pharmaceutically acceptable r or diluent and, as active ingredient, a therapeutically effective amount of a compound according to the invention, in particular a compound according to Formula (I), an N—oxide, a pharmaceutically acceptable salt thereof, a solvate thereof or a stereochemically isomeric form thereof, more in ular, a compound according to Formula (I), a pharmaceutically acceptable salt f, a solvate thereof or a stereochemically isomeric form thereof.
The carrier or diluent must be "acceptable" in the sense of being compatible with the other ingredients of the composition and not deleterious to the recipients thereof.
The nds according to the invention, in particular the compounds according to Formula (I), the N—oxides thereof, the pharmaceutically acceptable salts thereof, the solvates and the stereochemically isomeric forms thereof, more in particular the compounds according to Formula (I), the pharmaceutically acceptable salts f, the solvates and the stereochemically isomeric forms thereof, or any subgroup or ation thereofmay be formulated into various pharmaceutical forms for administration purposes. As riate compositions there may be cited all compositions usually employed for systemically administering drugs.
The pharmaceutical compositions of this invention may be ed by any methods well known in the art of pharmacy, for example, using methods such as those described in Gennaro et al. Remington’s Pharmaceutical Sciences (18th ed., Mack Publishing Company, 1990, see especially Part 8: Pharmaceutical preparations and their Manufacture). To prepare the pharmaceutical compositions of this invention, a eutically effective amount of the particular nd, optionally in salt form, as the active ingredient is combined in intimate admixture with a pharmaceutically acceptable carrier or diluent, which carrier or t may take a wide variety of forms depending on the form of preparation desired for administration. These pharmaceutical compositions are desirable in unitary dosage form suitable, in particular, for oral, topical, rectal or aneous administration, by parenteral injection or by inhalation.
For example, in preparing the compositions in oral dosage form, any of the usual pharmaceutical media may be employed such as, for example, water, glycols, oils, alcohols and the like in the case of oral liquid preparations such as, for example, sions, syrups, s, emulsions and solutions; or solid carriers such as, for example, starches, sugars, kaolin, diluents, lubricants, binders, egrating agents and the like in the case of powders, pills, capsules and tablets. Because of the ease in administration, oral stration is red, and tablets and capsules represent the most advantageous oral dosage unit forms in which case solid pharmaceutical carriers are obviously ed. For eral compositions, the carrier will usually comprise sterile water, at least in large part, though other ingredients, for example, tants, to aid solubility, may be included. Injectable solutions, for example, may be prepared in which the carrier comprises saline solution, glucose solution or a mixture of saline and glucose solution. Injectable suspensions may also be prepared in which case appropriate liquid carriers, suspending agents and the like may be employed. Also included are solid form preparations that are intended to be converted, shortly before use, to liquid form preparations. In the itions suitable for percutaneous administration, the carrier optionally comprises a ation enhancing agent and/or a le wetting agent, optionally combined with suitable additives of any nature in minor proportions, which additives do not uce a significant deleterious effect on the skin. Said ves may facilitate the administration to the skin and/or may be helpful for preparing the desired compositions. These compositions may be administered in various ways, e.g., as a transdermal patch, as a n, as an ointment.
It is especially advantageous to formulate the aforementioned pharmaceutical compositions in unit dosage form for ease of administration and uniformity of dosage.
Unit dosage form as used herein refers to physically discrete units suitable as unitary dosages, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effect in association with the required 2014/061478 ceutical carrier. Examples of such unit dosage forms are tablets (including scored or coated s), es, pills, powder packets, wafers, suppositories, injectable ons or suspensions and the like, teaspoonfuls, tablespoonfuls, and segregated multiples thereof.
Since the compounds according to the invention are orally administrable compounds, pharmaceutical compositions comprising aid compounds for oral administration are ally advantageous.
In order to enhance the solubility and/or the stability of the compounds of Formula (I) in pharmaceutical compositions, it can be advantageous to employ 0L-, [3- or y—cyclodextrins or their tives, in particular hydroxyalkyl substituted cyclodextrins, e.g. 2-hydroxypropyl-B-cyclodextrin or sulfobutyl-B-cyclodextrin. Also co-solvents such as alcohols may improve the solubility and/or the stability of the compounds according to the invention in pharmaceutical itions.
The exact dosage and frequency of administration depends on the particular compound of formula (I) used, the particular condition being treated, the severity of the condition being treated, the age, , sex, extent of disorder and general al condition of the particular patient as well as other medication the individual may be taking, as is well known to those skilled in the art. Furthermore, it is evident that said effective daily amount may be lowered or increased depending on the response of the treated subject and/or depending on the evaluation of the physician prescribing the compounds of the instant invention.
Depending on the mode of administration, the pharmaceutical composition will comprise from 0.05 to 99 % by weight, preferably from 0.1 to 70 % by weight, more preferably from 0.1 to 50 % by weight of the active ingredient, and, from 1 to 99.95 % by weight, preferably from 30 to 99.9 % by weight, more ably from 50 to 99.9 % by weight of a pharmaceutically acceptable carrier, all percentages being based on the total weight of the composition.
The amount of a compound of Formula (I) that can be ed with a carrier material to produce a single dosage form will vary depending upon the disease treated, the mammalian species, and the particular mode of administration. However, as a general guide, suitable unit doses for the compounds of the present invention can, for example, preferably n between 0.1 mg to about 1000 mg of the active nd.
A preferred unit dose is between 1 mg to about 500 mg. A more preferred unit dose is between 1 mg to about 300 mg. Even more preferred unit dose is between 1 mg to about 100 mg. Such unit doses can be administered more than once a day, for example, 2, 3, 4, 5 or 6 times a day, but ably 1 or 2 times per day, so that the total dosage for a 70 kg adult is in the range of 0.001 to about 15 mg per kg weight of subject per administration. A preferred dosage is 0.01 to about 1.5 mg per kg weight of subject per administration, and such therapy can extend for a number of weeks or months, and in some cases, years. It will be understood, however, that the specific dose level for any particular patient will depend on a variety of factors including the activity of the specific compound employed; the age, body weight, general health, sex and diet of the individual being treated; the time and route of administration; the rate of excretion; other drugs that have previously been administered; and the severity of the particular disease oing therapy, as is well understood by those of skill in the area.
A typical dosage can be one 1 mg to about 100 mg tablet or 1 mg to about 300 mg taken once a day, or, multiple times per day, or one time-release capsule or tablet taken once a day and containing a proportionally higher content of active ingredient. The time-release effect can be obtained by capsule als that dissolve at different pH , by capsules that release slowly by osmotic pressure, or by any other known means of lled release.
It can be ary to use dosages outside these ranges in some cases as will be apparent to those skilled in the art. Further, it is noted that the clinician or treating physician will know how and when to start, interrupt, adjust, or terminate therapy in conjunction with individual patient response.
As already mentioned, the invention also relates to a pharmaceutical composition comprising the compounds according to the ion and one or more other drugs for use as a ment or for use in the treatment, prevention, control, amelioration, or reduction of risk of diseases or ions for which compounds of Formula (I) or the other drugs may have utility. The use of such a composition for the manufacture of a medicament as well as the use of such a composition for the manufacture of a ment in the treatment, prevention, control, amelioration or reduction of risk of diseases or conditions for which nds of Formula (I) or the other drugs may have utility are also contemplated. The present invention also relates to a combination of a compound according to the present invention and an additional drug selected from the group of ychotics; NMDA receptor antagonists (e. g. memantine); NR2B antagonists; acetylcholinesterase inhibitors (e. g. donepezil, galantamine, physostigmine and rivastigmine) and/or antidepressant neurotransmitter reuptake inhibitors. In particular, the t ion also relates to a combination of a compound according to the present invention and antipsychotic(s), or to a combination of a compound according to the present invention and memantine and/or an NR2B antagonist. The present invention also relates to such a combination for use as a medicine. The present invention also relates to a product comprising (a) a compound according to the present invention, an N—oxide thereof, a pharmaceutically able salt thereof or a solvate thereof, in particular, a pharmaceutically able salt thereof or a e thereof, and (b) an additional component selected from antipsychotics, NMDA receptor antagonists (e.g. memantine), NR2B nists, acetylcholinesterase inhibitors and/or antidepressant neurotransmitter reuptake inhibitor(s), as a combined preparation for simultaneous, separate or sequential use in the ent or prevention of a condition in a mammal, including a human, the treatment or prevention of which is affected or facilitated by the neuromodulatory effect ofmGluR2 allosteric modulators, in ular negative mGluR2 allosteric modulators. More in particular the additional component (b) is selected from antipsychotic(s) or ine and/or an NRZB antagonist. The different drugs of such a combination or product may be combined in a single preparation er with pharmaceutically acceptable carriers or diluents, or they may each be present in a separate preparation together with pharmaceutically acceptable carriers or diluents.
The ing es are intended to illustrate but not to limit the scope of the present invention.
Chemistry Several s for preparing the compounds of this invention are rated in the following Examples. Unless otherwise noted, all starting materials were obtained from cial ers and used without further purification.
Hereinafter, "Boc" or "BOC" means tert—Butyloxycarbonyl; "CI" means chemical ionisation; "DAD" means diode-array detector; "THF" means tetrahydrofilran; "TEA" means triethylamine; "DIPE" means diisopropylether; "DMF" means N,N—dimethylformamide; "Et20" means diethylether; "EtOAc" means ethyl acetate; "DCM" means dichloromethane; "DMSO" means dimethylsulfoxide; "L" means liter; "LRMS" means low-resolution mass spectrometry/spectra; "HATU" means 2-(7-aza-1H-benzotriazoleyl)- l l ,3 ,3 -tetramethyluronium hexafluorophosphate; "HPLC" means high performance liquid chromatography; "HRMS" means high-resolution mass spectrometry/spectra; "mL" or "ml" means milliliter; "NH4Ac" means ammonium acetate; "EtOH" means ethanol; "ES" means electrospray; "iPrOH" means isopropanol; "iPrNH2" means isopropylamine; "MeOH" means methanol; "eq" means equivalent(s); "RP" means Reverse Phase; "rt" means room temperature; "M.p." means melting point; "min" means s; "h" means hour(s); "s" means second(s); "TOF" means time of flight; "QTOF" means pole-Time of Flight; "sat." means saturated; "SFC" means supercritical fluid chromatography; "sol." means solution.
Microwave ed reactions were performed in a single-mode reactor: InitiatorTM Sixty EXP microwave reactor (Biotage AB), or in a multimode reactor: MicroSYNTH Labstation (Milestone, Inc.).
Thin layer chromatography (TLC) was carried out on silica gel 60 F254 plates (Merck) using reagent grade solvents. Open column chromatography was performed on silica gel, particle size 60 A, mesh = 230-400 ) using standard techniques.
Automated flash column tography was performed using ready-to- t cartridges on irregular silica gel, particle size 15-40 um (normal phase disposable flash s) on different flash systems: either a SPOT or LAFLASH systems from Armen Instrument, or PuriFlash® 43Oevo systems from Interchim, or 971- FP systems from Agilent, or Isolera lSV systems from Biotage.
Nuclear Magnetic Resonance (NMR): For a number of compounds, 1H NMR spectra were recorded either on a Bruker Avance III, on a Bruker DPX-400 or on a Bruker AV-SOO spectrometer with standard pulse sequences, operating at 400 MHz and 500 MHz, respectively. Chemical shifts (8) are reported in parts per million (ppm) downf1eld from tetramethylsilane (TMS), which was used as internal standard.
Synthesis of Intermediate Compounds ediate I (I-1) 2H-Pyrazolecarboxylic acid ethyl ester (LI) /\O / HN \ N’ SulfiJric acid (10 mL, 187.6 mmol) was added to a solution of l-H-pyrazole carboxylic acid (1.93 g, 17.22 mmol) in EtOH (20 mL). The mixture was stirred at 90 0C for 15 h. Then it was allowed to cool to rt and the solvents were evaporated in vacuo. The residue was poured into water and the solution basified with K2C03 and extracted with EtOAc. The c layer was separated, dried (MgSO4), filtered and the solvent evaporated in vacuo to yield intermediate compound I-1 as a white solid (2.28 g, 93 % , 94%) which was used in the following step without further purification.
Intermediate 2 (1-2) 4-Iodo-2H-pyrazolecarboxylic acid ethyl ester (1-2) /\O / HN \ N’ Intermediate 1-1 (100 g, 0.68 mol), N—iodosuccinimide (213.5 g, 0.95 mol) were dissolved in DCM (2 L). The mixture was stirred at rt for 24 h. The mixture was treated with a sat. sol. ofNa2S203 and a sat. sol. ofNa2C03 and extracted with DCM. The c layer was separated, dried (MgSO4), filtered and the solvent evaporated in vacuo to yield intermediate compound 1-2 as a white solid (160 g, 85%).
Intermediate 3 (1-3) (2R-Hydroxy-propyl)-carbamic acid tert—butyl ester (I-3) roam Di-tert—butyl dicarbonate (58.1 g, 266.3 mmol) in DCM (50 mL) was added to a stirred on of (R)-(-)aminopropanol in DCM (50 mL) at 0 0C under nitrogen. The mixture was stirred at rt for 2 h. The mixture was diluted with cooled water and extracted with DCM. The c layer was separated, dried (Na2SO4), d and the solvents ated in vacuo to yield intermediate 1-3 as a colorless oil (47 g, quant.).
The t was used in the next step without further purification.
Intermediate 4 (1-4) (2S—Hydroxy-propyl)-carbamic acid tert—butyl ester (1-4) O)‘NH Intermediate compound 1-4 was synthesized following a similar approach described for intermediate 1-3. Starting from (S)-(-)aminopropanol (3 mL, 38.1 mmol), intermediate compound 1-4 was obtained as a colorless oil (6.13 g, 89% purity, 82%), that solidified upon standing at rt.
Intermediate 5 (1-5) roxy-propyl)-carbamic acid tert—butyl ester (1-5) Intermediate compound 1-5 was synthesized ing a similar approach described for intermediate 1-3. Starting from 1-aminopropanol (3 mL, 38.1 mmol), ediate compound 1-5 was obtained as a colorless oil (6.69 g, 98%).
Intermediate 6 (1-6) 2-(2-tert—Butoxycarbonylamino- 1S—methyl-ethyl)—4-iodo-2H-pyrazolecarboxylic acid ethyl ester (1-6) 2"NH \ A o \\s\ O N O Di-tert—butyl azodicarboxylate (4.67 g, 20.3 mmol) was added to a stirred solution of intermediate 1-2 (3 g, 11.28 mmol), intermediate 1-3 (4.44 g, 22.55 mmol) and triphenylphosphine (5.32 g, 20.3 mmol) in THF (56 mL) under nitrogen. The mixture was stirred at rt for 5 h. The t was evaporated in vacuo and the crude product was triturated with DIPE. The solid was filtered and the filtrate was evaporated in vacuo.
The crude product was purified by flash column chromatography (silica; EtOAc in Heptane 0/100 to 30/70). The desired fractions were collected and the solvents evaporated in vacuo to give intermediate compound 1-6 as a colorless oil (4.9 g, 91% purity, 93%).
Intermediate 7 (1-7) 2-(2-tert—Butoxycarbonylamino-1R-methyl-ethyl)iodo-2H-pyrazolecarboxylic acid ethyl ester (I-7) Intermediate compound I-7 was synthesized following a similar approach described for intermediate I-6. Starting from intermediate I-2 (1.18 g, 4.44 mmol) and intermediate I-4 (1.75 g, 8.87 mmol), intermediate compound I-7 was obtained as a white solid as two fractions (790 mg, 41%) and (900 mg, 86% purity, 41%).
Intermediate 8 (LS) 2-(2-tert—Butoxycarbonylaminomethyl-ethyl)iodo-2H-pyrazolecarboxylic acid ethyl ester (I-8) 0%N\H\( o) N O Intermediate compound I-8 was synthesized following a similar approach described for intermediate I-6. Starting from ediate I-2 (2.87 g, 10.79 mmol) and intermediate LS (3.78 g, 21.6 mmol), intermediate compound I-8 was obtained as a colorless oil (3.46 g, 75%). ediate 9 (L9) 2-(2-tert—Butoxycarbonylamino-ethyl)iodo-2H-pyrazolecarboxylic acid ethyl ester (L9) ON; 0) Intermediate compound I-9 was synthesized following a r approach bed for intermediate I-6. ng from intermediate I-2 (3.18 g, 11.95 mmol) and N—(tert— butoxycarbonyl)ethanolamine (3.78 g, 23.9 mmol), intermediate compound I-9 was obtained as a colorless oil (3.46 g, 75%).
Intermediate 10 (I-10) 2-(2-tert—Butoxycarbonylamino-1S—methyl-ethyl)-2H-pyrazolecarboxylic acid ethyl ester (I-10) film A N O Intermediate compound I-10 was synthesized following a similar approach described for intermediate I-6. Starting from intermediate I-1 (25.82 g, 184.25 mmol) and intermediate I-3 (47.16 g, 239.5 mmol), intermediate compound I-10 was obtained as a yellow oil (123 g, quant) which was used in the following step without fiarther purification.
Intermediate 11 (I-11) 2-(2-Amino-1S—methyl-ethyl)iodo-2H-pyrazolecarboxylic acid ethyl ester hydrochloride salt (I-11) A 4M solution of HCl in 1,4-dioxane (10 mL, 40 mmol) was added to a on of intermediate L6 (4.2 g, 9.63 mmol) in acetonitrile (20 mL). The e was stirred at 80 0C for 2 h. The solvent was evaporated in vacuo to yield intermediate compound I- 11 (3.5 g, 97%).
Intermediate 12 (I-12) 2-(2-Amino-1S—methyl-ethyl)-2H-pyrazolecarboxylic acid ethyl ester hydrochloride salt (I-12) H‘s O .HCl Intermediate compound I-12 was synthesized following a similar approach described for intermediate I-11. Starting from intermediate I-10 (54.79 g, 184.25 mmol) and a 4M on of HCl in 1,4-dioxane (415 mL, 1.66 mol), ediate compound I-12 was obtained as a white solid (32.5 g, 82% purity, 75%) which was used in the following step without further purification.
Intermediate 13 (I-13) 3-Iodo-7S—methyl-6,7-dihydro-5H—pyrazolo[ l ,5-a]pyrazinone (I-13) O I Intermediate I-11 as HCl salt (180 g, 350.4 mmol) was dissolved in a sat. sol. of NaHC03 (2 L). The mixture was stirred at rt for 12 h. The mixture was diluted with water and extracted with DCM. The organic layers were separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo. Then the residue was washed with tert- butyl methyl ether to yield intermediate nd I-13 (92 g, 90%), mp l82.6- C. 1H NMR (500 MHz, DMSO-d6) 5 ppm 1.42 (d, J=6.65 Hz, 3 H) 3.26 - 3.35 (m, l H) 3.57 - 3.71 (m, l H) 4.44 - 4.60 (m, l H) 7.68 (s, l H) 8.26 (br. s., l H). LC- HRMS (ESI+) Calculated for C7HgIN30 (M+H)+: 277.9790, Found: m/Z 277.9796 (+0.6mDa), Rt = 0.76 min (Method 13, see table 2). [a] = +ll.7o (589 nm, c 1.00 w/v %, CHgOH, 25 CC). ediate 13a ) (7S)—3-Bromo—7-methyl-6,7-dihydro-5H—pyrazolo [l ,5-a]pyrazinone (1-13a) ’N o 0 N \\ | Br \ w Bra / 0 ______. _>HN + I-3 N,N N\N .HCI |-11a L13a ediate l3a was prepared in 71% yield according to the following general description of a synthesis performed at a large scale: A mixture of methyl 4-bromo-lH—pyrazole-5 -carboxylate (referred to as "pyrazole SM" herein) (1 eq.), triphenyl phosphine (l.2 eq.), L3 (1.2 eq.) and anhydrous THF (15 mL/g le SM) under nitrogen was cooled to 5-10 oC. Di-tert-butyl azodicarboxylate (l .2 eq.) was added in portions at 5-15 0C under nitrogen. The solution was heated to 20-30 0C and stirred at 20-30 0C for 2-3 h. The obtained solution was concentrated and co-evaporated with isopropyl acetate to remove THF to afford a solution of crude 4-bromo- l -[(l S)- l -[[(l l -dimethylethoxy)carbonyl]amino]ethyl]- lH— pyrazolecarboxylic acid methyl ester I-6a in isopropyl acetate (20 mL/g pyrazole SM). To the solution of I-6a was bubbled HCl gas at 15-30 0C until cleavage of the Boc ting group was completed. The suspension was bubbled with nitrogen gas to remove most of the HCl gas. The suspension was concentrated to a volume of about 5 mL/g pyrazole SM below 50 CC, and then isopropyl acetate (15 mL/g pyrazole SM) was added to the e. Water (10 mL/g le SM) was added at 10-20 0C. The mixture was stirred at 10-20 CC for 20-30 min. The mixture was d and the aqueous layer was separated. The organic layer was extracted with water (2 mL/g pyrazole SM). The combined aqueous layers were washed with isopropyl acetate (2 x mL/g pyrazole SM) to remove al triphenylphosphine oxide. I-11a was obtained as an aqueous solution (6.25 mL/g pyrazole SM). To the aqueous solution of I-11a was added potassium carbonate (~1 g/g pyrazole SM) to adjust to pH=8-9 at 10- 25 CC. The mixture was stirred at 10-25 CC for 5-6 h and solid I-13a precipitated. The suspension was cooled to 5-10 oC and stirred at 5-10 0C for 2-3 h, it was then filtered and washed with water (1 mL/g pyrazole SM) and heptanes (1 mL/g pyrazole SM), then dried in vacuo at 40-45 CC to afford I-13a as a white solid, mp. 196.12 °C. 1H NMR (500 MHz, CDC13)8 ppm 1.61 (d, J=6.36 Hz, 3 H) 3.48 (ddd, J=12.72, 7.22, 2.60 Hz, 1 H) 3.75 - 3.84 (m, 1 H) 4.49 - 4.59 (m, 1 H) 6.54 (br. s., 1 H) 7.56 (s, 1 H).
LC-HRMS (ESI+) Calculated for C7H8BI'N30 (M+H)+: 229.9929, Found: m/z 229.9931 (+0.2mDa), Rt = 0.62 min (Method 13, see table 2). [0t] =+25.2 O (589 nm, c 0.53 w/v %, DMF, 20 oC).
Intermediate 14 (I-14) 7S-Methyl-6,7-dihydro-5H-pyrazolo[1,5-a]pyrazinone (I-14) §fN\N Intermediate compound I-14 was synthesized ing a similar approach described for intermediate I-13. ng from intermediate I-12 (32.5 g, 139.1 mmol), ediate compound I-14 was obtained as a solid (14.8 g, 70%).
Intermediate 15 (I-15) 3 -Iodo-7R-methyl-6,7-dihydro-5H-pyrazolo[1,5-a]pyrazinone (I- 1 5) '4ngK/m ’ A 4M solution of HCl in oxane (2.3 mL, 9.2 mmol) was added to a solution of intermediate I-7 (0.78 g, 1.84 mmol) in CH3CN (8.3 mL). The mixture was stirred at 80 0C for 7 h. After Boc deprotection was complete, part of the solvent was evaporated in vacuo and the on was basified with a sat. sol. of NaHC03. The mixture was stirred for 16 h at rt. Then the e was diluted with water and extracted with DCM.
The organic layers were separated, dried (MgSO4), filtered and the solvents evaporated in vacuo. The solid was triturated with DIPE to yield intermediate compound I-15 as a white solid (0.42 g, 82%).
Intermediate 16 (I-16) 3-Iodomethyl-6,7-dihydro-5H-pyrazolo[1,5-a]pyrazinone (I-16) O I Intermediate compound I-16 was sized following a similar approach described for intermediate I-15. Starting from intermediate LS (3.46 g, 8.17 mmol), intermediate compound I-16 was obtained as a white solid (1.87 g, 82%).
Intermediate 17 (I-17) 3 6,7-dihydro-5H-pyrazolo[1,5-a]pyrazinone (LI 7) O I HN)S%$K/N‘N/ Intermediate nd I-17 was synthesized following a similar approach described for intermediate I-15. Starting from intermediate I-9 (4.89 g, 11.95 mmol), intermediate compound I-17 was obtained as a white solid (1.87 g, 59%).
Intermediate 18 (I-18) 7S—Methyl(2-methyl-pyridinyl)-6,7-dihydro-5H-pyrazolo[1 ,5 -a]pyrazinone (I- §f / Pd(PPh3)4 (0.33 g, 0.29 mmol) was added to a stirred suspension of intermediate I-13 (1.6 g, 5.77 mmol) and 2-picolineboronic acid (0.95 g, 6.93 mmol) in 1,4-dioxane (8 mL) and a sat. sol. ofNaHC03 (4 mL) in a sealed tube under en. The mixture was stirred at 100 0C for 16 h. Then the mixture was diluted with H20 and extracted with DCM. The organic layer was separated, dried (Na2SO4), d and the solvent evaporated in vacuo. The crude product was purified by flash column chromatography (silica; MeOH in DCM 0/100 to 6/94). The desired fractions were ted and the solvents ated in vacuo to yield intermediate compound I-18 as a white solid (1 g, 71%), mp 173.20 °C. 1H NMR (500 MHz, CDClg) 8 ppm 1.67 (d, J=6.65 Hz, 3 H) 2.60 (s, 3 H) 3.52 (ddd, J=12.79, 7.15, 2.89 Hz, 1 H) 3.84 (dt, J=12.72, 4.00 Hz, 1 H) 4.57 - 4.66 (m, 1 H) 6.10 (br. s., 1 H) 7.51 (dd, J=5.20, 1.44 Hz, 1 H) 7.55 (s, 1 H) 7.78 (s, 1 H) 8.50 (d, J=5.20 Hz, 1 H). LC-HRMS (ESI+) Calculated for C13H14IN4O (M+H)+: 46, Found: m/z 243.1250 (+0.4mDa), Rt = 0.82 min (Method 13, see table 2). [ct] 0 (589 = +328 nm, c 0.52 w/v %, DMF, 20 CC).
Intermediate I-18 was alternatively prepared in 70% yield according to the following general description of a synthesis performed at a large scale: A mixture of I-13a (1 eq.), 2-methyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolanyl)- pyridine (1.1 eq.), anhydrous potassium phosphate (2 eq.), DME (7.5 mL/g I-13a) and purified water (2.5 mL/g I-13a) was evacuated and backfilled with nitrogen 3 times.
Triphenyl phosphine (0.261 eq.) and palladium (II) acetate (0.131 eq.) were added in one portion under nitrogen. The mixture was evacuated and led with nitrogen 3 times again, it was heated to 75-80 0C and stirred at 75-80 0C for 12-15 h under nitrogen. The aqueous layer was separated at 60-70 0C and discarded, and then water (8 mL/g I-13a) was added to the organic layer. DME was removed by concentration below 40 oC. Isopropyl acetate (15 mL/g I-13a) was added, the pH of the e was adjusted to 1-2 with cone. HCl. The mixture was filtered and the filter cake was washed with water (1 mL/g I-13a), the aqueous layer was ted and the organic layer was extracted with water (2 mL/g I-13a). The ed aqueous layers were washed with Isopropyl acetate (2 x 15 mL/g I-13a). The aqueous layer was concentrated to remove residual DME and isopropyl e. MTBE (2 mL/g I-13a) was added and the mixture was cooled to 0-5 oC, stirred at 0-5 0C for 2-3 h. I-18 was filtered, washed with cooled water (1 mL/g , and dried in vacuum at 45-50 CC to afford I-18 as an off-white solid.
Intermediate 19 (I-19) 7R-Methyl(2-methyl-pyridinyl)-6,7-dihydro-5H-pyrazolo[1 ,5 -a]pyrazinone (I- _ 86 _ ediate compound I-19 was synthesized following a similar approach described for intermediate 1-18. Starting from intermediate 1-15 (0.62 g, 2.24 mmol), intermediate compound I-19 was obtained as a white solid (0.38 g, 70%).
Intermediate 20 (1-20) 7-Methyl(2-methyl-pyridinyl)-6,7-dihydro-5H-pyrazolo[ l ,5 -a]pyrazinone (I- KVNrN/ Intermediate compound 1-20 was synthesized following a similar approach bed for ediate 1-18. ng from intermediate 1-16 (846 mg, 3.05 mmol), intermediate compound 1-20 was obtained as a yellowish solid (585 mg, 79%).
Intermediate 18 (1-18) and ediate 19 (1-19) 7S-Methyl(2-methyl-pyridinyl)-6,7-dihydro-5H-pyrazolo[ l ,5 -a]pyrazinone (1-18) and 7R-Methyl(2-methyl-pyridinyl)-6,7-dihydro-5H-pyrazolo[l ,5- a]pyrazinone (1-19). §f / (M8) (M9) Intermediate 1-20 (975 mg, 4.02 mmol) was purified by RP HPLC (Stationary phase: irregular bare silica 40 g), Mobile phase: 0.5% NH4OH, 95% DCM, 5% MeOH) then by chiral SFC ((Stationary phase: CHIRALCEL® OD-H 5um 250x20mm), (Mobile phase: 75% C02, 25% iPrOH (0.3% iPrNH2)) to yield intermediate compound 1-18 (390 mg) and intermediate compound 1-19 (395 mg).
Intermediate 21 (1-21) 3 -(2-Methyl-pyridinyl)—6,7-dihydro-5H-pyrazolo[ 1 ,5 -a]pyrazinone (1-2 1) Intermediate compound I-21 was synthesized following a similar approach described for intermediate I-18. Starting from ediate 1-17 (908 mg, 3.45 mmol), intermediate compound I-21 was ed as a white solid (0.5 g, 63%).
Intermediate 22 (I-22) 7S—Methyl(4-trifluoromethyl-phenyl)-6,7-dihydro-5H-pyrazolo [1 ,5-a]pyrazinone (I-22) §fN/N\ A mixture of intermediate 1-14 (5 g, 33.01 mmol), copper(I) iodide (3.78 g, 19.85 mmol) and K2C03 (9.14 g, 66.15 mmol) in toluene (150 mL) was nitrogen flushed for a few min. Then 4-bromobenzotrifluoride (9.3 mL, 66.1 mmol) and N,N- dimethylethylenediamine (2.1 mL, 19.8 mmol) were added. The mixture was stirred under nitrogen at rt for 10 min and then stirred at 100 0C for 16 h. Then, DMF (20 mL) was added and the mixture was stirred at 100 0C for 8 h. Then water, a conc. sol. of ammonia and DCM were added. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo. The crude product was purified by flash column chromatography (silica; EtOAc in DCM 0/100 to 50/50). The desired fractions were collected and the ts evaporated in vacuo to yield intermediate compound I-22 as a pale yellow oil (9.6 g, 98%).
Intermediate 23 (I-23) 3-Iodo-7S—methyl(4-trifluoromethyl-phenyl)-6,7-dihydro-5H-pyrazolo [1,5 -a]pyrazinone (I-23) WO 95311 §fN/N\ Iodine (11.55 g, 45.5 mmol) was added to a solution of intermediate I-22 (19.2 g, 65.0 mmol) and ammonium (IV) nitrate (24.95 g, 45.5 mmol) in acetonitrile (350 mL). The mixture was d at 70 0C for 1 h. Then the mixture was diluted with EtOAc and washed with a sat. sol. ofNa2S203 and brine. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo. The residue was precipitated with DIPE and then was purified by short column chromatography (silica, DCM) then by flash column chromatography (silica; DCM in heptane 50/50 to 100/0). The desired fractions were ted and the solvents evaporated in vacuo to yield intermediate compound I-23 as a solid (24.8 g, 90%).
Intermediate 24 (I-24) 2-Amino-pyridineboronic acid (I-24) HO\ ,OH N NH2 2-Aminochloropyridine (3g, 23.34 mmol) was added to a mixture of bis(pinacolato)diboron (17.78 g, 70.01 mmol), 2-dicyclohexylphosphino-2’,6’- dimethoxybiphenyl (0.38 g, 0.93 mmol), tris(dibenzylideneacetone)dipalladium(0) (0.21 g, 0.23 mmol) and ium acetate (3.89 g, 39.67 mmol) in 1,4-dioxane (78 mL) under nitrogen atmosphere. The resulting mixture was stirred at 100 0C for 3 h.
The hot reaction mixture was filtered through aceous earth and washed with EtOAc. The organic layer was evaporated in vacuo. The residue was precipitated with DIPE to yield intermediate compound I-24 as a white solid (5.84 g, quant.) that was used in the next reaction step without further purification.
Intermediate 25 (I-25) 3 -(2-Methoxy-pyridinyl)-7S-methyl-6,7-dihydro-5H-pyrazolo [1 ,5-a]pyrazinone (I-25) §f / Pd(PPh3)4 (0.42 g, 0.36 mmol) was added to a stirred suspension of intermediate I-13 (2 g, 7.22 mmol) and 2-methoxypyridineboronic acid (1.77 g, 11.55 mmol) in 1,4- dioxane (16 rnL) and a sat. sol. ofNaHC03 (8 rnL) in a sealed tube under en here. The mixture was stirred at 100 0C for 3 days. Then the mixture was diluted with H20 and extracted with DCM. The organic layer was separated, dried (Na2SO4), filtered and the solvent evaporated in vacuo. The crude product was purified by flash column chromatography (silica; MeOH in DCM 0/100 to 6/94). The desired fractions were collected and the solvents evaporated in vacuo to yield intermediate compound I-25 as a pale brown solid (1.6 g, 86%).
Intermediate 26 and final compound 215 (I-26 and Co. No. 215) 3-(2-Chloro-pyridinyl)-7S—methyl(4-trifluoromethyl-phenyl)—6,7-dihydro-5H- lo[l,5-a]pyrazinone (I-26 and Co. No. 215) This reaction was divided in four batches to a combined total amount indicated herein and combined for workup and purification. 3)4 (401 mg, 0.35 mmol) was added to a stirred suspension of ediate I-23 (2.92 g, 6.94 mmol) and 2-chloropyridine- nic acid (1.42 g, 9.02 mmol) in 1,4-dioxane (39 rnL) and a sat. sol. ofNaHC03 (19.5 rnL). The mixture was stirred at 150 0C for 10 min under microwave irradiation.
Then the mixture was diluted with H20 and extracted with DCM. The organic layer was separated, dried (Na2SO4), filtered and the solvent evaporated in vacuo. The crude product was purified by flash column chromatography (silica; EtOAc in DCM 0/100 to . The desired fractions were collected and the solvents evaporated in vacuo to yield intermediate compound I-26 as a yellow solid (1.84 g, 65%).
WO 95311 Intermediate 27 (I-27) 7S—Methyl(4-trifiuoromethyl-phenyl)(2-vinyl-pyridinyl)-6,7-dihydro-5H- pyrazolo[1 ,5 -a]pyrazinone (I-27) §f / Pd(PPh3)4 (51 mg, 0.044 mmol) was added to a stirred suspension of intermediate I-26 (600 mg, 1.48 mmol) and Vinylboronic acid pinacolester (0.325 mL, 1.92 mmol) in 1,4- dioxane (10 mL) and a sat. sol. 03 (5 mL). The mixture was stirred at 150 0C for 15 min under microwave irradiation. Then the mixture was diluted with H20 and ted with DCM. The organic layer was separated, dried (Na2SO4), filtered and the solvent evaporated in vacuo. The crude product was purified by flash column chromatography (silica; EtOAc in DCM 0/100 to 30/70). The desired fractions were collected and the solvents ated in vacuo to yield intermediate compound I-27 as a yellow oil (0.53 g, 90%).
Intermediate 28 (I-28) Ethyl 2-[ 1 - [(tert—butoxycarbonylamino)methyl] [tert-butyl(dimethyl)silyl]oxy-ethyl] - 4-iodo-pyrazolecarboxylate (I-28) Di-tert—butyl azodicarboxylate (1.97 g, 8.53 mmol) was added to a stirred solution of 4- iodo-1H—pyrazolecarboxylic acid ethyl ester (1.26 g, 4.74 mmol), [3 -(tertbutyldimethylsilanyloxy )hydroxypropyl]carbamic acid tert—butyl ester (2.90 g, 9.48 mmol) and triphenylphosphine (2.24 g, 8.53 mmol) in THF (23.6 mL) under nitrogen atmosphere. The mixture was stirred at rt for 2.5 h. The t was evaporated and the e was treated with DIPE. The solid (PthO) was filtered off and the filtrate was evaporated in vacuo. The crude product was purified by flash column chromatography (silica; DCM in Heptane 50/50 to 100/0 then EtOAc in DCM 0/100 to 3/97). The desired fractions were collected and concentrated in vacuo to yield intermediate compound 1-28 (2.57 g, 98%) as a colorless oil.
Intermediate 29 (I-29)_ Ethyl 2-[ l -(aminomethyl)hydroxy-ethyl] iodo-pyrazole-3 -carboxylate hydrochloride salt (1-29) . HCl Hydrochloric acid (4 M in l,4-dioxane, 5.80 mL, 23.21 mmol) was added to a stirred solution of intermediate 1-28 (2.57 g, 4.64 mmol) in CH3CN (21 mL). The mixture was stirred at rt for l h. The e was trated in vacuo to yield intermediate compound 1-29 (1 .69 g) as a beige solid which was used in the next step without any further purification. ediate 30 (1-30) 7-(Hydroxymethyl)iodo-6,7-dihydro-5H-pyrazolo[ l ,5 -a]pyrazinone (1-30) o N/ TEA (l .38 mL, 9.93 mmol) was added to a stirred solution of intermediate 1-29 (1 .68 g, 4.48 mmol) in DMF (16.8 mL). The mixture was stirred at rt for 3 h. The mixture was d with a sat. sol. ofNaHC03 and EtOAc and filtered. The filtrate was partitioned between water and EtOAc and extracted with EtOAc and EtOAc/THF. The c layer was separated, dried (Na2SO4), filtered and concentrated in vacuo. The crude product was purified by flash column chromatography (silica; MeOH in DCM 0/100 to /80). The desired fractions were collected and concentrated in vacuo to yield ediate compound 1-30 (0.88 g, 67%) as a white solid.
Intermediate 3 I (L3 1) roxymethyl)-3 -(2-methylpyridyl)-6,7-dihydro-5H-pyrazolo[ l ,5 -a]pyrazin one (L3 1) Pd(PPh3)4 (134 mg, 0.12 mmol) was added to a d suspension of intermediate I-30 (0.88 g, 3.00 mmol) and 2-picolineboronic acid (658 mg, 3.00 mmol) in 1,4-dioxane (15.4 mL) and a sat. aq. NaHC03 (10 mL) under en atmosphere. The mixture was stirred at 90 0C for 16 h. Then additional 2-picolineboronic acid (263 mg, 1.20 mmol) and Pd(PPh3)4 (35 mg, 0.03 mmol) were added at rt and under nitrogen. The mixture was d at 100 0C for 7 h. Then the mixture was d with water and extracted with EtOAc. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo. The crude product was purified by flash column chromatography (silica; MeOH in DCM 0/100 to . The desired fractions were collected and concentrated in vacuo to yield intermediate compound I-31 (347 mg, 45%) as pale orange solid.
Intermediate 32 (I-32) 7-(Hydroxymethyl)-6,7-dihydro-5H-pyrazolo [l ,5-a]pyrazinone (L32) Wk?»/ Palladium 10% on charcoal (907 mg, 0.0.853 mmol) was added to a solution of intermediate I-30 (2.5 g, 8.53 mmol) and TEA (4.74 mL, 3412 mmol) in DMF (125 mL) under nitrogen atmosphere. The mixture was hydrogenated (at atmospheric pressure) at rt for 16 h. The mixture was filtered through a pad of diatomaceous earth and the residue was washed with MeOH and 7M solution of ammonia in MeOH. The filtrate was concentrated in vacuo and the residue was treated with a small amount of water and extracted with EtOAc/THF. The c layer was separated, dried (Na2SO4), filtered and concentrated in vacuo to yield intermediate compound I-32 (1.4 g, quant.) as a brown oil.
Intermediate 33a (I-33a) and ediate 33b (I-33b) (7S)—7-methyl-3 -(4,4,5 ,5 -tetramethyl- l ,3 xaborolanyl)-5 -[4- (trifiuoromethyl)phenyl]-6,7-dihydropyrazolo[l ,5-a]pyrazinone (I-33a) and [(7S)methyloxo[4-(trifiuoromethyl)phenyl]-6,7-dihydropyrazolo- [l,5-a]pyrazin-3 -yl]boronic acid (I-33b) F F F ijsz. F o HO F o B/o F o B/OH §f / "M/ N\ N\ N §f N (L33a) (L33b) Isopropylmagnesium chloride lithium chloride complex (1 .3M solution, 32.9 mL, 42.7 mmol) was added dropwise to a stirred solution of intermediate I-23 (10 g, 23.7 mmol) and 2-z's0propoxy-4,4,5,5-tetramethyl-l,3,2-dioxaborolane (9.7 mL, 47.5 mmol) in anhydrous THF (100 mL) at -25 0C under en atmosphere. The e was stirred for 30 min at -25 0C. Then the reaction was quenched with a 10% NH4Cl aq sol. and extracted with EtOAc. The organic layer was separated, dried (Na2804), filtered and the solvents evaporated in vacuo. The crude product was purified by flash column chromatography (silica; MeOH in DCM 0/100 to 3/97). The desired fractions were collected and the solvents evaporated in vacuo. The crude product was triturated with DIPE, filtered and dried to yield intermediate compound I-33a (6.4 g, 64%) as a white solid. The solution and impure fractions from the column purification were combined and repurified by flash column chromatography (silica, EtOAc in e 30/70 to . The desired fractions were collected and the ts evaporated in vacuo. The product was triturated in DIPE/Heptane, filtered and dried to yield intermediate compound I-33b (l g, 10%) as a white solid.
Intermediates I-34 to I-37 The following intermediates were synthesized by following an analogous synthetic procedure as reported for intermediate 22. _ 94 _ Structure Intermediate number Startin_ materials Intermediate 38 and final compound 170 (7S)—5 -(3 ,4-dichlor0phenyl)methyl-3 -(2-methyl- l -0xid0-pyridin- l -iumyl)-6,7- dihydropyrazolo[l,5-a]pyrazinone (I-38 and Co. No. 170) 3-Chloroperoxybenzoic acid (2.03 g, 11.77 mmol) was added to a stirred solution of intermediate I-34 (2.28 g, 5.88 mmol) in DCM (37 mL) at 0 0C. The mixture was allowed to reach rt and d at rt for 2 h. The mixture was treated with a sat sol. of Na2C03 and diluted with DCM. The organic layer was separated, dried (Na2SO4), lO filtered and the solvents evaporated in vacuo to yield intermediate compound I-38 (1.84 g, 77%) that was used in the next step t any further purification.
W0 2014/195311 _ 95 _ Intermediate 39 (L39) 4- [(7S)-5 -(3 hlorophenyl)methyloxo-6,7-dihydropyrazolo[1,5 -a]pyrazin-3 - yl]pyridinecarbaldehyde (I-39) N / §f / Manganese dioxide (2.39 g, 27.57 mmol) was added to a solution of final compound 125 (E-14) (1.11 g, 2.75 mmol) in chloroform (11.7 mL). The mixture was stirred at rt for 16 h, at 60 0C for 5 h and then at rt for 16 h. Then, the mixture was filtered through a pad of diatomaceous earth and washed with DCM. The solvent was evaporated in vacuo. The crude product was purified by flash column chromatography (silica; EtOAc in DCM 0/100 to . The desired ons were collected and evaporated in vacuo to yield intermediate compound I-39 (537 mg, 48%) as a pale yellow solid.
Intermediate 40 (I-40) The following intermediate was synthesized by following an analogous tic orocedure as re oorted for intermediate 39.
Intermediate number n_ material Intermediate 41 (I-41) tert—Butyl 4-(5-chloropyridyl)piperazine- 1-carboxylate (L41) 1504* A mixture of 2-bromochloropyridine (1.5 g, 7.79 mmol), 1-BOC-piperazine (2.18 g, 11.69 mmol), sodium tert—butoxide (1.49 g, 15.59 mmol), 9,9-dimethyl-4,5- bis(diphenylphosphino)xanthene (0.451 g, 0.78 mmol) and tris(dibenzylideneacetone)dipalladium(0) (0.357 g, 0.390 mmol) in toluene (25 mL) was stirred at 120 CC for 16 h. The mixture was poured into water, and extracted with EtOAc. The mixture was filtered through a short pad of aceous earth. The c layer was separated, washed with water and brine, dried (MgSO4) and evaporated in vacuo. The crude product was purified by flash column chromatography a, EtOAc in DCM 0/100 to 20/80). The desired fractions were collected and evaporated in vacuo to yield intermediate compound I-41 (0.888 g, 38%) as an orange solid.
Intermediate 42 (I-42) tert—Butyl 4-[5-[(7S)methyloxo[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo [l ,5 -a]pyrazin-3 -yl] idyl]piperazine- l -carboxylate (I-42) A suspension of intermediate I-41 (478 mg, 1.60 mmol), intermediate I-33a (653 mg, 1.55 mmol), palladium(II) acetate (7 mg, 0.032 mmol), 2-dicyclohexylphosphino-2',6'- dimethoxybiphenyl (26 mg, 0.064 mmol) and K2C03 (554 mg, 4.013 mmol) in CH3CN (l .6 mL) and H20 (2.5 mL) was flushed with nitrogen for a few minutes and the mixture was stirred at 80 0C for 24 h. Then the mixture was d with H20 and extracted with EtOAc. The organic layer was separated, dried (Na2804), filtered and the solvent evaporated in vacuo. The crude product was purified by flash column chromatography (silica; EtOAc in DCM 0/100 to 50/5 0). The desired fractions were collected and evaporated in vacuo to yield intermediate compound I-42 (663 mg, 74%) as a yellow oil.
Intermediate 43 and final nd 188 (7S)—5-[6-chloro(trifiuoromethyl)pyridyl]methyl(2-methylpyridyl)-6,7- dihydropyrazolo[l,5-a]pyrazinone (I-43 and Co. No. 188) 3)4 (47 mg, 0.041 mmol) was added to a stirred suspension of ediate 1-18 (100 mg, 0.413 mmol), 2,6-dichloro(trifluoromethyl)pyridine (86 uL, 0.620 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (47 mg, 0.082 mmol), CS2C03 (269 mg, 0.825 mmol) in 1,4-dioxane (3 mL) in a sealed tube and under nitrogen. The mixture was stirred at 120 0C for 4 h. The mixture was filtered through a pad of diatomaceous earth and washed with DCM. The filtrate was evaporated in vacuo. The crude product was purified by flash column chromatography (silica, EtOAc in DCM 0/100 to 30/70). The desired fractions were collected and concentrated in vacuo. Then the product was triturated with EtzO and d to yield intermediate compound 1-43 (71 mg, 40%) as a white solid.
Intermediate 44 (1-44) 7-(Difluoromethyl)-5 -[4-(trifiuoromethyl)phenyl]pyrazolo[ 1 ,5 azinone (1-44) NA?» Diethylaminosulfur trifluoride (0.373 mL, 3.866 mmol) was added to a stirred solution of intermediate 1-40 (297 mg, 0.966 mmol) in DCM (33 mL) at 0 0C. The mixture was allowed to warm to rt and stirred for 5 h. Then additional diethylaminosulfur trifiuoride (0.355 mL, 2.9 mmol) was added at 0 0C and the mixture was stirred at rt for 20 h. The mixture was treated with water and extracted with DCM. The organic layer was separated, dried (Na2SO4), filtered and concentrated in vacuo. The crude product was purified by flash column chromatography (silica; DCM). The desired fractions were collected and concentrated in vacuo to yield intermediate compound 1-44 (258 mg, 81%) as a colorless oil.
Intermediate 45 (1-45) The ing intermediate was sized by following an analogous tic procedure as reported for intermediate 23. _ 98 _ Intermediate number n_ materials Intermediate 46 (I-46) The following intermediate was synthesized by following an analogous synthetic orocedure as re oorted for intermediate 18 U:a I 42%7—5 flL }O\./ I-47 I-48 i) NH3 (28% in water, 54 mL) was added over 2-[1-[[(l,ldimethylethyl )dimethylsilyl]oxy]ethy1]-oxirane (4.73 g, 23.373 mmol) and the mixture was stirred at 120 CC for 40 min under microwave irradiation. The solvent was then concentrated in vacuo to yield intermediate compound I-47 as an orange oil (3.298 g, 64%). ii) Intermediate I-48 was synthesized ing an analogous synthetic procedure as reported for intermediate I-3. Starting from intermediate I-47 (3.269 g, 14.9 mmol), intermediate compound I-48 was ed as a colorless oil (4.642 g, 97.5%).
Intermediates 49-52 (I-49 to I-52) The following ediates were synthesized by following an analogous synthetic procedure as reported for intermediate 6. _ 99 _ Structure Intermediate number Startin_ materials N—(2-hydroxybutyl)— carbamic acid 1,1- dimethylethyl ester N—(2—hydroxy methylpropyl)—carbamic acid 1, l -dimethy1ethy1 ester 1-48 —\O IN,N\ tert—butylN—(2-hydroxy 1'52 O HVNTOK ypropyl)carbamate Intermediate 53 (1-53) The following intermediate was synthesized following the procedure for the synthesis of intermediate 1-29, followed by the procedure for the sis of ediate 1-30.
Structure Intermediate number Starting materials «V»/ ‘N 1-53 1-51 ediate 54 (I-54) Ethyl 2-[ l -(aminomethyl)—2-methoxy-ethyl]iodo-pyrazolecarboxylate (I-54) _\ I \_N 0 WNHZ .HCl HCl (4 M in dioxane, 2.2 mL, 8.82 mmol) was added to a solution of intermediate I-52(0.8 g, 1.765 mmol) in CH3CN (8 mL). The mixture was stirred at rt for l h and then the solvent was concentrated in vacuo to give intermediate compound I-54 (700 mg, 87%) as a cream solid.
Intermediate 55 (I-55) 3-Iodo(methoxymethyl)-6,7-dihydro-5H-pyrazolo [1 ,5-a]pyrazinone (I-55) Eth (0.55 mL, 3.98 mmol) was added to a solution of intermediate I-54 (0.7 g, 1.80 mmol) in DMF (6.7 mL). The mixture was d at rt for 3 h then neutralized with a sat. sol. ofNaHC03 and extracted with DCM. The organic layer was separated, dried 4), filtered and the solvents evaporated in vacuo to give intermediate compound I-55 (440 mg, 80%) as a white solid. ediates 56 and 57 (I-56 and I-57) The following intermediates were synthesized by following an analogous synthetic procedure as that reported for intermediate 15. -lOl- Structure Intermediate number n_ material Intermediates 58-61 (1-58 to 1-61) The following intermediates were synthesized by following an ous synthetic procedure as reported for intermediate 25.
Structure Intermediate number Startin_ materials 2-picolineboronic acid 1-56 2-picolineboronic acid I-57 2-picolineboronic acid 1-53 2-picolineboronic acid Intermediate 62 (L62) 2- [( l S)(3 ,4-dichloroanilino)- l -methyl-ethyl] (2-methylpyridyl)pyrazole-3 - carboxylic acid (I-62) Sodium hydride (60% dispersion in mineral oil, 20 mg, 0.344 mmol) was added to a on of nd Co. No. 6a (200 mg, 0.516 mmol) in DMF (4 mL) and the mixture was stirred at 60 0C for 24 h. Then more sodium hydride (60% dispersion in mineral oil, ll mg, 0. 172 mmol) was added and the mixture was stirred at 60 0C for 3 h. Then, the mixture was quenched with a NH4Cl sat. sol. and extracted with EtOAc.
The organic layer was separated, dried (MgSO4), filtered and the solvents evaporated in vacuo to give intermediate compound I-62 (230 mg, tative) as a solid which was used in the next step without r purification.
Intermediate 63 (L63) 2- [( l S)(4,5 -dichloroiodo-anilino)- l -methyl-ethyl] (2-methyl pyridyl)pyrazolecarboxylic acid (I-63a) and 2-[(lS)(3,4-dichloroiodo-anilino)- l-methyl-ethyl](2-methylpyridyl)pyrazole-3 xylic acid (I-63b) (I-63a) (I-63b) N—iodosuccimide (124 mg, 0.552 mmol) was added to a solution of intermediate nd I-62 (224 mg, 0.5523 mmol) in chloroform (5 mL) and the mixture was stirred at rt for 3 h. Then more N—iodosuccimide (62 mg, 0.277 mmol) was added and the mixture was stirred at rt for 18 h. Then the reaction was quenched with a sat. sol. of Na2803 and extracted with DCM. The organic layer was separated, dried (MgSO4), filtered and the solvent ated in vacuo to give a mixture of intermediates compounds I-63a and I-63b (240 mg, 41%) which was used in next step without further purification.
Intermediate 64 (I-64) tert—Butyl N-[[2,2,2-trifluoro(nitromethyl)ethyl]amino]carbamate (I-64) F30? )(HN’0A0 tert—Butyl carbazate (281 mg, 2.13 mmol) was added to a stirred solution of 3,3,3- trifluoro-l-nitro-propene (prepared as described in J. Fluorine Chem. 2008, 767- 774) (73 uL, 0.709 mmol) in MeOH (3.1 rnL) at rt. The mixture was stirred for 1 h and the solvents ated in vacuo. The crude product was purified by flash column chromatography (silica, EtOAc in Heptane 40/60 to 60/40) to yield intermediate compound 1-64 (200 mg, quant.) Intermediate 65 (I-65) -Trifluoro(nitromethyl)ethyl]hydrazine hydrochloride salt (I-65) F30? HCl (6M in 1,4-dioxane, 10.5 mL, 42 mmol) was added to a solution of intermediate 1-64 (1.15 g, 4.2 mmol) in MeOH (10 mL) at rt. The mixture was stirred for 2 h and the solvents were evaporated in vacuo to yield intermediate compound 1-65 (880 mg, quant.) that was used in the next step without filrther purification.
Intermediate 66 (I-66) Ethyl 2-[2,2,2-trifluoro(nitromethyl)ethyl]pyrazolecarboxylate (I-66a) and ethyl 1 - [2,2,2-trifluoro(nitromethyl)ethyl]pyrazole-3 -carboxylate (I-66b) OZN/YNEHOJ /\ Intermediate 67 (I-67) 7-Methyl-6,7-dihydro-5H-pyrazolo[l ,5-a]pyrazinone (1-67) HM)?»/ KKN‘N Pd (10% on charcoal, 100 mg, 0.094 mmol) and um formate (112 mg, 1.78 mmol) were added to a stirred solution of intermediate 1-66 (100 mg, 0.355 mmol) in MeOH (3.3 mL). The mixture was stirred in a sealed tube at 70 0C for 2 h. The t was concentrated in vacuo to yield intermediate compound 1-67 (70 mg, 96%) that was used in the ing step without further purification.
Intermediate 68 (1-68) 3 -Iodo(trifluoromethyl)-5 - [4-(trifluoromethyl)phenyl]-6,7-dihydropyrazolo[ l ,5 - a]pyrazinone (1-68) KrN‘N/ Intermediate compound 1-68 was synthesized by following the sequence of an analogous synthetic procedure as reported for intermediate 1-22 starting from intermediate I-67 and 4-bromobenzotrifluoride, followed by the procedure for intermediate 1-23.
Final Compounds (7S)—7-Methyl-3 -(2-methylpyridinyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[l,5-a]pyrazin-4(5H)-one (E-l, Co. No. 1) Procedure A: Copper(I) iodide (872 mg, 4.58 mmol) was added to a stirred suspension of ediate I-18 (1.85 g, 7.64 mmol), 4-bromobenzotrifluoride (2.14 mL, 15.27 mmol), K2C03 (2.11 g, 15.27 mmol) and N,N'-dimethylethylenediamine (0.492 mL, 4.58 mmol) in toluene (70 mL) in a sealed tube and under nitrogen. The mixture was stirred at 100 0C for 16 h. Then DMF (10 mL) was added and the mixture was stirred at 100 0C for onal 8 h. The mixture was filtered through diatomaceous earth and washed with EtOAc. The organic layer was washed with d NH4OH sol, dried (Na2SO4), filtered and the solvents evaporated in vacuo. The crude product was purified by flash column chromatography (silica; EtOAc in e 20/80 to 50/50).
The desired fractions were collected and the solvents evaporated in vacuo. The product was precipitated with e, filtered and dried in vacuo to yield final product compound 1 as a white solid (2.32 g, 78%). 1H NMR (500 MHz, CDClg) 5 ppm 1.75 (d, J=6.4 Hz, 3 H), 2.57 (s, 3 H), 4.02 (dd, J=12.7, 7.2 Hz, 1 H), 4.30 (dd, J=12.6, 4.2 Hz, 1 H), 4.75 - 4.84 (m, 1 H), 7.44 (d, J=5.2 Hz, 1 H), 7.49 (d, J=3.8 Hz, 2 H), 7.51 (s, 1 H), 7.71 (d, J=8.4 Hz, 2 H), 7.80 (s, 1 H), 8.48 (d, J=5.2 Hz, 1 H).
Procedure B: Copper(I) iodide (94 mg, 0.495 mmol) was added to a stirred suspension of intermediate I-18 (200 mg, 0.825 mmol), 4-bromobenzotrifluoride (0.231 mL, 1.651 mmol), K2C03 (228 mg, 1.65 mmol) and imethylethylenediamine (53 uL) in toluene (7.5 mL) in a sealed tube and under nitrogen. The mixture was stirred at 100 0C overnight. The mixture was d through a pad of diatomaceous earth and washed with DCM. The organic layer was separated, dried (MgSO4), filtered and the solvents evaporated in vacuo. The crude product was d by flash column chromatography (silica, EtOAc in Heptane 0/100 to 70/30). The desired fractions were collected and concentrated in vacuo to yield compound 1 (283 mg, 89%) as a pinkish solid.
Procedure C: Pd(PPh3)4 (384 mg, 0.332 mmol) was added to a stirred suspension of intermediate I-23 (2 g, 4.74 mmol) and 2-methylpyridineboronic acid pinacol ester (1.66 g, 7.60 mmol) in 1,4-dioxane (10 mL) and a sat. sol. ofNa2C03 (5 mL) in a sealed tube under nitrogen. The e was stirred at 100 0C for 16 h. Then the mixture was diluted with H20 and extracted with DCM and DCM with a small amount of EtOH. The organic layer was dried (Na2SO4), filtered and the solvent evaporated in vacuo. The crude product was purified by flash column chromatography (silica; 7M solution of ammonia in MeOH in DCM 0/100 to 3/97 then EtOAc in Heptane 0/100 to 100/0). The desired fractions were collected and evaporated in vacuo to yield nd 1 as a white solid (480 mg, 26%). (1.31 g of starting material was recovered).
Procedure D; general description of a synthesis performed at a large scale by which Co.
No. 1 was isolated in 90% yield before purification: A mixture of I-18 (1 eq.), potassium carbonate (2 eq.), (I) iodide (0.3 eq.), 4- bromobenzotrifiuoride (1.3 eq.), N,N'-Dimethyl ethylenediamine (0.35 eq.), DMF (5 mL/g I-18) and toluene (8 mL/g I-18) was evacuated and backfilled with nitrogen 3 times. It was heated to 0 CC and stirred at 100-110 CC for 7-8 h under en.
The reaction solution was trated to remove toluene below 50 oC. Isopropyl acetate (15 mL/g I-18) was added. The mixture was washed with 5% NH4OH aqueous solution (3 x 7 mL/g I-18), and then 5% N—acetyl-L-cysteine and 5% K2C03 aqueous solution (2 x 7 mL/g I-18) at 10-25 0C. Finally, it was washed with 5% NaCl aqueous solution (5 mL/g I-18). The obtained solution was concentrated and co-evaporated with MTBE to remove isopropyl acetate. The resulting solid was filtered and dried in vacuo at 45-50 0C. Co. No. 1 was obtained as an off-white solid which was r purified as follows: Co. No. 1 was ved in a solvent mixture of IPA (4 mL/g Co. No. 1) and water (1 mL/g Co. No. 1) at 48-55 0C. The solution was filtered and cooled to 0-5 0C. An IPA/water mixture (0.5 mL/g Co. No. 1, 4/1 v/v) was used to rinse. Water (650 uL/g Co. No. 1) was added drop-wise and seeding with Co. No. 1 was med. The mixture was stirred at 0-5 0C for 3-4 h. Water (14 mL/g Co. No. 1) was added drop- wise at 0-5 0C for 3-4 h, and then the suspension was stirred at 0-5 0C for 5-6 h. The wet product was filtered and rinsed with water (2 mL/g Co. No. 1), then dried in vacuo at 45-50 0C for 16 h to afford Co. No. 1 as a white solid.
For compound 1 (DSC mp = 155.35 0C), the hydrochloride salt (.HCl) (DSC mp = decomposes above 200 0C); the sulfate salt (.H2804) (DSC mp = decomposes above 200 CC); the methane sulfonate salt (.CHgSOgH) (DSC mp = 252 CC); and the maleate salt CH=CHC02H-cz's) (DSC mp = 163 oC); wherein the mp were determined by DSC (Mettler Toledo Q2000 MDSC, heating from 25 to 350 0C at 10 oC /min) were obtained following the procedure described below: Compound 1 (1.5 g) in 9 mL of IPA or acetone chloride and sulfate salts were generated in acetone; methanesulfonate and maleate salts were generated in IPA) were stirred at 50 0C until all the solid was dissolved. The acid (1.1 mol equivalents) was added to the solution and the reaction mixture was further stirred for 2 h at 50 CC, then cooled to 20 0C in 1 h and further stirred for 30 h at 20 oC. The suspension was filtered and the solids were dried at 50 0C in a vacuum oven overnight. (7S)—7-Methyl-3 -pyridinyl[4-(trifiuoromethyl)phenyl]-6,7-dihydropyrazolo [1,5-a]pyrazin-4(5H)-one (E-2, Co. No. 2) §f / Pd(PPh3)4 (41 mg, 0.036 mmol) was added to a stirred suspension of intermediate I-23 (300 mg, 0.71 mmol) and pyridineboronic acid (114 mg, 0.93 mmol) in 1,4-dioxane (3.3 mL) and a sat. sol. ofNaHC03 (1.5 mL). The mixture was stirred at 150 0C for 10 min under microwave irradiation. Then the mixture was diluted with H20 and extracted with DCM. The c layer was separated, dried (Na2SO4), filtered and the solvent evaporated in vacuo. The crude product was purified by flash column chromatography (silica; MeOH in DCM 0/100 to 6/94). The desired fractions were collected and the solvents evaporated in vacuo. The residue was purified by ion exchange tography using an ISOLUTE® SCX2 cartridge eluting first with MeOH and then with 7M solution of a in MeOH. The desired fractions contained in the 7M solution of ammonia in MeOH were collected and the solvents evaporated in vacuo.
The residue was precipitated with DIPE to yield compound 2 as a white solid (215 mg, 81%). 1H NMR (400 MHz, CDClg) 8 ppm 1.76 (d, J=6.5 Hz, 3 H), 4.03 (dd, J=12.7, 7.2 Hz, 1 H), 4.31 (dd, J=12.7, 4.2 Hz, 1 H), 4.81 (qdd, J=6.7, 6.7, 6.7, 6.5, 4.3 Hz, 1 H), 7.51 (d, J=8.1 Hz, 2 H), 7.65 (dd, J=4.4, 1.6 Hz, 2 H), 7.71 (d, J=8.3 Hz, 2 H), 7.83 (s, 1 H), 8.60 (dd, J=4.6, 1.8 Hz, 2 H). (7S)(2-Aminopyridinyl)methyl[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[l,5-a]pyrazin-4(5H)-one (E-3, Co. No. 71) N\N/ Pd(PPh3)4 (96 mg, 0.083 mmol) was added to a stirred suspension of ediate I-23 (700 mg, 1.66 mmol) and intermediate I-24 (458 mg, 3.32 mmol) in 1,4-dioxane (10 mL) and a sat. sol. ofNaHC03 (5 mL). The mixture was stirred at 150 0C for 10 min under microwave irradiation. Then the mixture was diluted with H20 and extracted with DCM. The organic layer was separated, dried (Na2SO4), filtered and the solvent evaporated in vacuo. The crude product was purified by flash column chromatography a; MeOH in DCM 0/100 to 10/90). The desired fractions were collected and the solvents evaporated in vacuo and the residue was purified by RP HPLC (RP C18 XBridgeTM 30 x 100 mm 5 um), mobile phase (gradient from 67% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 33% CH3CN to 50% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 50% CH3CN). The residue was purified by ion exchange tography using an ISOLUTE® SCX2 cartridge g first with MeOH and then with 7M solution of ammonia in MeOH. The d fractions contained in the 7M solution of ammonia in MeOH were collected and the solvents evaporated in vacuo to yield final product compound 71 as a white solid (163 mg, %). 1H NMR (500 MHz, CDC13)5 ppm 1.74 (d, J=6.4 Hz, 3 H) 4.01 (dd, J=12.6, 7.1 Hz, 1 H) 4.29 (dd, , 4.2 Hz, 1 H) 4.43 (br. s., 2 H) 4.78 , J=6.6, 4.3 Hz, 1 H) 6.94 (dd, J=5.5, 1.4 Hz, 1 H) 6.98 (s, 1 H) 7.51 (br. d, J=8.4 Hz, 2 H) 7.71 (br. d, J=8.4 Hz, 2 H) 7.79 (s, 1 H) 8.06 (d, J=4.9 Hz, 1 H).
Example 4 (7S)—3-[2-(Ethylamino)pyridyl]methyl[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[l,5-a]pyrazinone (E-4, Co. No. 44) H"/N\ Sodium triacetoxyborohydride (246 mg, 1.16 mmol) was added to a stirred solution of compound 71 (300 mg, 0.77 mmol) and acetaldehyde (0.048 mL, 0.85 mmol) in 1,2- dichloroethane (3 mL). The mixture was stirred at rt for 16 h. Then the mixture was diluted with a sat. sol. ofNaHC03 and ted with DCM. The organic layer was separated, dried (Na2SO4), filtered and the solvent evaporated in vacuo. The crude product was purified by flash column chromatography a; EtOAc in heptane 0/100 to 40/60). The desired fractions were ted and the solvents evaporated in vacuo.
The residue was purified by ion exchange chromatography using an ISOLUTE® SCX2 cartridge eluting first with MeOH and then with 7M solution of ammonia in MeOH.
The desired fractions ned in the 7M solution of ammonia in MeOH were collected and the solvents evaporated in vacuo and the residue was purified by RP HPLC (RP C18 XBridgeTM 30 x 100 mm 5 um), mobile phase (gradient from 60% 0.1% H/NH4OH pH 9 solution in Water, 40% CH3CN to 43% 0.1% NH4C03H/NH4OH pH 9 on in Water, 57% CH3CN). The residue was precipitated with DIPE to yield compound 44 as a white solid (28 mg, 9%). 1H NMR (500 MHz, CDC13)5 ppm 1.24 (t, J=7.2 Hz, 3 H) 1.74 (d, J=6.4 Hz, 3 H) 3.29 - 3.37 (m, 2 H) 4.00 (dd, J=12.6, 7.1 Hz, 1 H) 4.29 (dd, J=12.6, 4.2 Hz, 1 H) 4.42 (br. t, J=4.6 Hz, 1 H) 4.74 - 4.82 (m, 1 H) 6.83 (s, 1 H) 6.84 (dd, J=5.3, 1.3 Hz, 1 H) 7.51 (br. d, J=8.7 Hz, 2 H) 7.70 (br. d, J=8.7 Hz, 2 H) 7.79 (s, 1 H) 8.07 (d, J=5.5 Hz, 1 H).
Example 5 (7S)—3-(2-Methoxypyridyl)methyl[4-(trifiuoromethyl)phenyl]-6,7- dihydropyrazolo[l,5-a]pyrazinone (E-S, Co. No. 45) Copper(I) iodide (66 mg, 0.348 mmol) was added to a stirred suspension of intermediate I-25 (150 mg, 0.58 mmol), 4-bromobenzotrifluoride (209 mg, 0.93 mmol), K2C03 (161 mg, 1.16 mmol) and N,N-dimethylethylenediamine (0.037 mL, 0.348 mmol) in toluene (3.75 mL) in a sealed tube and under nitrogen. The mixture was stirred at 100 0C for 24 h. Then, more 4-bromobenzotrifiuoride (131 mg, 0.58 mmol) was added and the mixture was stirred at 100 0C for onal 16 h. The mixture was filtered through diatomaceous earth and washed with DCM. The c layer was evaporated in vacuo. The crude product was d by flash column chromatography (silica; EtOAc in Heptane 0/100 to 20/80). The desired fractions were collected and the solvents evaporated in vacuo. The product was precipitated with EtZO. The solid was purified by RP HPLC (RP C18 XBridgeTM 30 x 100 mm 5 um), mobile phase (gradient from 60% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 40% CH3CN to 43% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 57% CH3CN) to yield compound 45 as a white solid (130 mg, 56%). %). 1H NMR (500 MHz, CDClg) 8 ppm 1.75 (d, J=6.6 Hz, 3 H) 3.94 (s, 3 H) 4.02 (dd, J=12.7, 7.2 Hz, 1 H) 4.30 (dd, J=12.6, 4.2 Hz, 1 H) 4.75 - 4.83 (m, 1 H) 7.09 (s, 1 H) 7.23 (dd, J=5.5, 1.2 Hz, 1 H) 7.50 (br. d, J=8.7 Hz, 2 H) 7.70 (br. d, J=8.7 Hz, 2 H) 7.79 (s, 1 H) 8.14 (d, J=5.5 Hz, 1 H).
Example 6 -(2-Ethylpyridyl)methyl[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[l,5-a]pyrazinone (E-6, Co. No. 46) 2014/061478 H"/N\ A solution of intermediate I-27 (114 mg, 0.29 mmol) in EtOH (5.7 mL) was hydrogenated in a H-Cube® reactor (1 mL/min, 30 mm 2/C 20% cartridge, full H2 mode, rt, 1 cycle). Then, the solvent was evaporated in vacuo. The crude product was purified by RP HPLC (RP C18 XBridgeTM 30 x 100 mm 5 um), mobile phase (gradient from 60% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 40% CH3CN to 43% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 57% CH3CN) to yield compound 46 as a white solid (84 mg, 73%). 1H NMR (400 MHz, coon) 5 ppm 1.32 (t, J=7.6 Hz, 3 H) 1.75 (d, J=6.7 Hz, 3 H) 2.85 (q, J=7.6 Hz, 2 H) 4.02 (dd, J=12.7, 7.2 Hz, 1 H) 4.31 (dd, J=12.7, 4.2 Hz, 1 H) 4.80 (quind, J=6.7, 4.2 Hz, 1 H) 7.46 (dd, J=5.1, 1.6 Hz, 1 H) 7.48 (br. s, 1 H) 7.51 (br. d, J=8.3 Hz, 2 H) 7.71 (br. d, J=8.3 Hz, 2 H) 7.81 (s, 1 H) 8.51 (dd, J=5.3, 0.7 Hz, 1 H).
Example 7 1 5 7-(Hydroxymethyl)(2-methylpyridyl)[4-(trifluoromethyl)phenyl] -6,7- dihydropyrazolo[1,5-a]pyrazinone (E-7, Co. No. 87) Copper(I) iodide (0.135 g, 0.709 mmol) was added to a stirred sion of intermediate I-31 (305 mg, 1.18 mmol), 4-bromobenzotrifluoride (298 uL, 2.12 mmol), K2C03 (330 mg, 2.36 mmol) and N,N’-dimethylethylenediamine (76 uL, 0.71 mmol) in toluene (7.63 mL) in a sealed tube and under nitrogen. The mixture was stirred at 100 0C for 18 h. Then additional K2C03 (160 mg, 1.18 mmol), copper(I) iodide (0.067 g, 0.354 mmol), N,N’ hylethylenediamine (38 uL, 0.35 mmol) and 4- bromobenzotrifluoride (132 uL, 0.95 mmol) were added under nitrogen and the mixture was stirred at 100 0C for 5 h. The mixture was filtered through a pad of diatomaceous earth and washed with DCM. The organic layer was separated, dried 4), filtered and concentrated in vacuo. The crude product was purified by flash column chromatography (silica; ol in DCM 0/100 to 7/93). The d fractions were collected and concentrated in vacuo to yield compound 87 (321 mg, 68%) as yellow oil that precipitated upon standing at rt.
Example 8 7-(Fluoromethyl)(2-methylpyridyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[l,5-a]pyrazinone (E-8, Co. No. 52) (Diethylamino)sulfur ride (23 ML, 0.185 mmol) was added to a stirred solution of compound 87 (50 mg, 0.124 mmol) in DCM (2.4 mL) at -10 0C. The mixture was allowed to warm to rt and stirred for 18 h. The mixture was treated with water and extracted with DCM. The organic layer was separated, dried (Na2SO4), filtered and trated in vacuo. The crude product was purified by flash column chromatography (silica; EtOAc in DCM 0/100 to 100/0 and MeOH in EtOAc 0/100 to 1/99). The desired fractions were collected and concentrated in vacuo. Then the compound was triturated with DIPE to yield compound 52 (14.5 mg, 29%) as a white solid. 1H NMR (500 MHz, CDC13)5 ppm 2.58 (s, 3 H) 4.31 (dd, J=13.1, 4.8 Hz, 1 H) 4.47 - 4.53 (m, 1 H) 4.86 - 5.07 (m, 3 H) 7.45 (br. d, J=4.6 Hz, 1 H) 7.51 (br. d, J=8.7 Hz, 2 H) 7.50 (s, 1 H) 7.72 (br. d, J=8.7 Hz, 2 H) 7.85 (s, 1 H) 8.49 (d, J=5.2 Hz, 1 H).
Example 9 (7S)[4-Fluoro-3 -(trifluoromethyl)phenyl]methyl(2-methylpyridyl)-6,7- dihydropyrazolo[1,5-a]pyrazinone (E-9, Co. No. 67) Compound 67 was obtained ng from intermediate I-18 (160 mg, 0.66 mmol), 5- bromofluorobenzotrifluoride (149 uL, 1.06 mmol), N,N’ hylethylenediamine (42 uL, 0.396 mmol), copper(I) iodide (75 mg, 0.396 mmol), K2C03 (182mg, 1.32 mmol) in toluene (4.27 mL), following a ure similar to that described in E-l, yielding compound 67 (224 mg, 84%) as a pale yellow solid. 1H NMR (500 MHz, CDClg) 8 ppm 1.76 (d, J=6.4 Hz, 3 H) 2.58 (s, 3 H) 3.98 (dd, J=12.7, 7.2 Hz, 1 H) 4.25 (dd, J=12.6, 4.2 Hz, 1 H) 4.80 (quind, J=6.6, 4.3 Hz, 1 H) 7.29 (d, J=9.5 Hz, 1 H) 7.43 (dd, J=5.2, 1.2 Hz, 1 H) 7.48 (s, 1 H) 7.54 - 7.61 (m, 2 H) 7.80 (s, 1 H) 8.49 (d, J=5.2 Hz, 1 H).
Example 10 (7S)[4-(2-Flu0r0eth0xy)(trifluoromethyl)phenyl]methyl(2-methyl pyridyl)-6,7-dihydropyrazolo[1,5-a]pyrazinone (E-10, Co. No. 77) Sodium hydride (60% dispersion in mineral oil, 22 mg, 0.544 mmol) was added to a on of 2-fluoroethanol (453 uL, 0.495 mmol) in DMF (4.5 mL) at 0 0C and the e was stirred at rt for 10 minutes. Then compound 67 (200 mg, 0.495 mmol) was added. The mixture was stirred at 110 0C for 23 h. The on mixture was cooled to rt and a solution of 2-fluoroethanol (227 uL, 0.247 mmol) and Sodium hydride (60% dispersion in mineral oil, 12 mg, 0.297 mmol) in DMF (0.5 ml) was added. The resulting mixture was stirred at 110 0C for 16 h. The mixture was quenched with water and extracted with EtOAc. The organic layer was separated, dried (Na2SO4) and the solvents were evaporated in vacuo. The crude product was purified by flash column chromatography (silica; 7M solution of ammonia in MeOH in DCM/ DCM 0/100 to 2/98). The desired fractions were collected and the solvents evaporated in vacuo to afford 164 mg of compound 77, which was fiarther purified by RP HPLC (Stationary phase: C18 XBridgeTM 30 x 100 mm 5 um), mobile phase: nt from 67% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 33% CH3CN to 50% 0.1% NH4C03H/NH4OH pH 9 on in Water, 50% CH3CN), yielding 125 mg of compound 77, which was further purified by RP HPLC (Stationary phase: C18 XBridgeTM 30 x 100 mm 5 um), mobile phase: Gradient from 67% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 33% CH3CN to 50% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 50% CH3CN), yielding 117 mg of compound 77 which was further d by RP HPLC (Stationary phase: C18 XBridgeTM 30 x 100 mm 5 um), mobile phase: Gradient from 47% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 53% MeOH to 30% 0.1% NH4C03H/NH4OH pH 9 on in Water, 70% MeOH), ng compound 77 (39 mg, 18%), also recovering 38 mg of starting al, compound 67. For compound 77: 1H NMR (400 MHz, CDClg) 5 ppm 1.75 (d, J=6.5 Hz, 3 H) 2.57 (s, 3 H) 3.96 (dd, J=12.8, 7.3 Hz, 1 H) 4.24 (dd, , 4.4 Hz, 1 H) 4.28 - 4.38 (m, 2 H) 4.70 - 4.87 (m, 2 H) 4.75 - 4.83 (m, 1 H) 7.08 (d, J=8.6 Hz, 1 H) 7.44 (dd, J=5.2, 1.3 Hz, 1 H) 7.48 - 7.57 (m, 3 H) 7.79 (s, 1 H) 8.47 (dd, J=5.3, 0.5 Hz, 1 H).
Example 11 (7S)(4-Ethoxyphenyl)methyl(2-methylpyridyl)-6,7-dihydropyrazolo [1 ,5 - a]pyrazinone hydrochloride salt (E-l 1, Co. No. 81) . HCl Copper(I) iodide (47 mg, 0.247 mmol) was added to a stirred suspension of intermediate I-18 (0.1 g, 0.413 mmol), 4-iodophenetole (0.164 g, 0.661 mmol), K2C03 (114 mg, 0.825 mmol) and N,N’ -dimethylethylenediamine (26 uL, 0.211 mmol) in toluene (6 mL) in a sealed tube and under nitrogen. The mixture was stirred at 100 0C for 24 h. The mixture was filtered through a pad of diatomaceous earth and washed with DCM. The organic layer was evaporated in vacuo. The crude product was purified by flash column chromatography (silica; EtOAc in DCM 0/100 to 40/60). The desired fractions were collected and concentrated in vacuo to yield compound 81 as an oil. The residue was dissolved in EtOAc and HCl (4N) (103 uL, 0.413 mmol) was added. The residue was triturated from DIPE, filtered and dried in vacuo to yield compound 81 (163 mg, 99%) as a white solid. Free base: 1H NMR (300 MHz, CDClg) 8 ppm 1.35 (t, J=6.9 Hz, 3 H) 1.65 (d, J=6.5 Hz, 3 H) 2.50 (s, 3 H) 3.84 (dd, J=12.9, 7.0 Hz, 1 H) 3.97 (q, J=7.0 Hz, 2 H) 4.16 (dd, J=12.9, 4.3 Hz, 1 H) 4.60 - 4.76 (m, 1 H) 6.87 (br. d, J=8.8 Hz, 2 H) 7.18 (br. d, J=8.7 Hz, 2 H) 7.43 (br. d, J=4.8 Hz, 1 H) 7.48 (br. s, 1 H) 7.72 (s, 1 H) 8.39 (br. d, J=4.3 Hz, 1 H); HCl salt: 1H NMR (300 MHz, DMSO-d6) 5 ppm 1.34 —114— (t, J=6.9 Hz, 3 H) 1.60 (d, J=6.3 Hz, 3 H) 2.68 (s, 3 H) 3.38 (br. s., 1 H) 3.90 — 4.14 (m, 3 H) 4.28 (dd, J=13.0, 4.1 Hz, 1 H) 4.78 — 4.94 (m, 1 H) 7.00 (br. d, J=8.9 Hz, 2 H) 7.35 (br. d, J=8.8 Hz, 2 H) 8.23 — 8.42 (m, 3 H) 8.69 (d, J=6.3 Hz, 1 H).
Example 12 4-[(7S)Methyloxo[4-(trifiuoromethyl)phenyl]-6,7-dihydropyrazolo [l ,5 - a]pyrazinyl]pyridinecarbonitrile (E-12, Co. No. 127) Pd(PPh3)4 (42 mg, 0.036 mmol) was added to a stirred suspension of intermediate I-33a (250 mg, 0.593 mmol) and 4-bromopyridinecarbonitrile (162 mg, 0.884 mmol) in l,4-dioxane (4 mL) and a sat. sol. ofNa2C03 (2 mL). The e was stirred at 150 0C for 10 min under microwave irradiation. Then the mixture was diluted with H20 and extracted with DCM. The organic layer was dried 4), filtered and the solvent evaporated in vacuo. The crude t was purified by flash column chromatography (silica; EtOAc in DCM 0/100 to 50/50). The desired fractions were ted and evaporated in vacuo. The e was precipitated with DIPE. The solid was filtered to yield compound 127 as a white solid. 1H NMR (500 MHz, CDClg) 5 ppm 1.77 (d, J=6.4 Hz, 3 H) 4.05 (dd, J=l2.9, 7.4 Hz, 1 H) 4.32 (dd, J=l2.7, 4.0 Hz, 1 H) 4.79 - 4.88 (m, l H) 7.51 (br. d, J=8.4 Hz, 2 H) 7.74 (br. d, J=8.4 Hz, 2 H) 7.86 (s, l H) 7.92 (dd, J=5.2, 1.7 Hz, 1 H) 8.04 - 8.14 (m, l H) 8.67 (d, J=5.2 Hz, 1 H).
Example 13 (7S)—3-(2-Isopropylpyridyl)methyl[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[l,5-a]pyrazinone (E-13, Co. No. 126) Pd(PPh3)4 (26 mg, 0.022 mmol) was added to a stirred suspension of intermediate 1- 33b (150 mg, 0.442 mmol) and 4-bromoisopropyl-pyridine (prepared as described in WO2009/l 18292) (97 mg, 0.486 mmol) in a sat. aq. sol. NaHC03 (1 mL) and 1,4- WO 95311 e (1 mL). The mixture was stirred at 120 0C for 10 min under microwave irradiation. The mixture was filtered through aceous earth and washed with DCM. The organic layer was washed with water, separated, dried (Na2SO4), filtered and concentrated in vacuo. The crude product was purified by flash column chromatography ((silica; 7N solution of ammonia in MeOH in DCM 0/100 to 10/90) then (silica, EtOAc in DCM 0/100 to 30/70)) then by RP HPLC onary phase: C18 XSelectTM 19 x 100 mm 5 um, Mobile phase: Gradient from 80% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 20% CH3CN to 0% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 100% CH3CN)). The desired fractions were collected and evaporated in vacuo to yield compound 126 as a white solid. 1H NMR (400 MHz, CDClg) 8 ppm 1.32 (d, J=6.9 Hz, 6 H) 1.75 (d, J=6.7 Hz, 3 H) 3.08 (spt, J=6.9 Hz, 1 H) 4.02 (dd, J=12.7, 7.2 Hz, 1 H) 4.31 (dd, J=12.6, 4.0 Hz, 1 H) 4.80 (quind, J=6.7, 4.3 Hz, 1 H) 7.45 - 7.48 (m, 2 H) 7.51 (br. d, J=8.3 Hz, 2 H) 7.71 (br. d, J=8.6 Hz, 2 H) 7.81 (s, 1 H) 8.50 - 8.55 (m, 1 H) Example 14 -(3,4-Dichlorophenyl)[2-(hydroxymethyl)pyridyl]methyl-6,7- dihydropyrazolo[l,5-a]pyrazinone (E-14, Co. No. 125) A sion of intermediate I-34 (1.09 g, 4.56 mmol) in acetic anhydride (8 mL) was stirred at 100 0C for 2 h. The mixture was cooled to rt, and poured into water (15 mL) and EtOAc (30 mL). The organic layer was separated, washed with a sat. NaHC03 sol., dried (Na2SO4), filtered and concentrated in vacuo. The resultant oil was stirred with lithium ide (259 mg, 10.81 mmol) in MeOH (5.45 mL) and H20 (2.72 mL) at rt for 30 min. Then, EtOAc was added and the organic layer was washed with water, brine, dried (Na2SO4), filtered and concentrated in vacuo. The crude product was purified by flash column chromatography a; 7M solution of ammonia in MeOH in DCM 0/100 to 3/97). The desired fractions were collected and evaporated in vacuo to yield compound 125 (670 mg, 61%).
Crude compound 125 (100 mg) was purified by RP HPLC (Stationary phase: C18 XBridge 30 x 100 mm 5 um), Mobile phase: Gradient from 54% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 46% CH3CN to 64% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 36% CH3CN) 72 mg compound , yielding 125. 1H NMR (500 MHz, CDC13) 5 ppm 1.74 (d, J=6.4 Hz, 3 H) 3.73 (br. s., 1 H) 3.96 (dd, J=12.7, 7.2 Hz, 1 H) 4.24 (dd, J=12.7, 4.3 Hz, 1 H) 4.72 — 4.83 (m, 3 H) 7.23 (dd, J=8.7, 2.3 Hz, 1 H) 7.49 (d, J=2.3 Hz, 1 H) 7.51 (d, J=8.7 Hz, 1 H) 7.55 (d, J=4.9 Hz, 1 H) 7.59 (s, 1 H) 7.82 (s, 1 H) 8.54 (d, J=4.9 Hz, 1 H).
Example 15 (7S)—5 -(3 ,4-Dichlorophenyl)-3 -[2-(1-hydroxyethyl)pyridyl]methyl-6,7- dihydropyrazolo[1,5-a]pyrazinone (E-15, Co. No. 111) magnesium chloride 3M in THF (249 uL, 0.747 mmol) was added dropwise to a solution of intermediate I-39 (150 mg, 0.374 mmol) in THF (1.24 mL) at -78 0C and under en. The mixture was stirred at -78 0C for 2 h. Then, more methylmagnesium chloride 3M in THF (125 uL, 0.374 mmol) was added and the mixture was stirred at -78 0C for 1 h. Then, it was quenched at -78 0C with a sat. NH4Cl sol. and allowed to reach rt. The e was extracted with EtOAc. The organic layer was separated, dried (MgSO4), filtered and the solvents evaporated in vacuo. The crude product was purified by flash column chromatography (silica; MeOH in DCM 0/100 to /95). The desired fractions were ted and evaporated in vacuo. The residue was precipitated with Ether/Heptane to yield compound 111 as a pale yellow solid. 1H NMR (400 MHz, CDC13) 8 ppm 1.52 (dd, J=6.6, 0.8 Hz, 3 H) 1.74 (dd, J=6.5, 2.3 Hz, 3 H) 3.91 - 4.02 (m, 1 H) 4.13 - 4.31 (m, 2 H) 4.72 - 4.84 (m, 1 H) 4.92 (q, J=6.5 Hz, 1 H) 7.23 (dd, J=8.6, 2.5 Hz, 1 H) 7.49 (d, J=2.3 Hz, 1 H) 7.51 (d, J=8.6 Hz, 1 H) 7.56 (br. d, J=5.3 Hz, 1 H) 7.59 - 7.63 (m, 1 H) 7.82 (s, 1 H) 8.52 (dd, J=5.1, 0.7 Hz, 1 H) Example 16 (7S)—7-Methyl-3 -(2-methyloxido-pyridiniumyl)-5 -[4-(trifluoromethyl)phenyl] - 6,7-dihydropyrazolo[1,5-a]pyrazinone (E-16, Co. No. 140) 3-Chloroperoxybenzoic acid (2.96 g, 17.18 mmol) was added to a stirred solution of final compound E-l (3.32 g, 8.59 mmol) in DCM (133 mL) at 0 0C. The mixture was d to reach rt and stirred at rt for 3 h. The mixture was treated with Na2C03 sat sol. and diluted with DCM. The organic layer was separated, dried 4), filtered and the solvents evaporated in vacuo to yield compound 140 (3.4 g, 98%) as a pale yellow solid.
A small fraction (350 mg) was purified by flash column chromatography a; MeOH in DCM 0/100 to 5/95). The desired fractions were collected and evaporated in vacuo.
The residue was precipitated with EtZO and filtered to yield pure compound 140 (290 mg, 8%). 1H NMR (500 MHz, CDClg) 8 ppm 1.75 (d, J=6.4 Hz, 3 H) 2.53 (s, 3 H) 4.02 (dd, J=12.7, 7.2 Hz, 1 H) 4.30 (dd, J=12.7, 4.0 Hz, 1 H) 4.75 - 4.85 (m, 1 H) 7.50 (d, J=8.4 Hz, 2 H) 7.63 (dd, J=6.8, 2.5 Hz, 1 H) 7.67 - 7.77 (m, 3 H) 7.81 (s, 1 H) 8.21 (d, J=6.6 Hz, 1 H).
Example 17 -[4-(1-Hydroxyethyl)phenyl]methyl-3 -(2-methylpyridyl)-6,7- dihydropyrazolo[l,5-a]pyrazinone (E-17, Co. No. 149) Sodium borohydride (6 mg, 0.166 mmol) was added to a stirred solution of intermediate I-35 (60 mg, 0.166 mmol) in MeOH (5 mL) at 0 0C. The mixture was stirred at rt for 16 h. The solvent was concentrated in vacuo. The e was dissolved with DCM and washed with a sat. Na2C03 sol. The organic layer was separated, dried (MgSO4), filtered and the solvents evaporated in vacuo. The crude product was purified by flash column chromatography (silica; MeOH in DCM 0/100 to 100/0). The d fractions were collected and concentrated in vacuo to yield compound 149 (40 mg, 66%). 1H NMR (300 MHz, CDClg) 5 ppm 1.52 (d, J=6.5 Hz, 3 H) 1.73 (d, J=6.5 Hz, 3 H) 2.31 (br. s., 1 H) 2.57 (s, 3 H) 3.97 (dd, J=12.8, 6.9 Hz, 1 H) 4.16 - 4.39 (m, 1 H) W0 2014/195311 2014/061478 4.60 — 4.86 (m, 1 H) 4.95 (q, J=6.4 Hz, 1 H) 7.35 (br. d, J=8.2 Hz, 2 H) 7.42 — 7.59 (m, 4 H) 7.81 (s, 1 H) 8.37 — 8.49 (m, 1 H).
Example 18 (7S)—5-(4-Cyclopropylphenyl)methyl(2-methylpyridyl)-6,7- dihydropyrazolo[1,5-a]pyrazinone (E-18, Co. No. 156) Pd(PPh3)4 (37 mg, 0.032 mmol) was added to a stirred sion of intermediate I-36 (255 mg, 0.642 mmol), cyclopropylboronic acid (165 mg, 1.92 mmol) and K2C03 (177 mg, 1.28 mmol) in CH3CN (5 mL) and H20 (2 mL). The mixture was stirred at 150 0C for 10 min under microwave irradiation. Then more cyclopropylboronic acid (165 mg, 1.92 mmol) and Pd(PPh3)4 (37 mg, 0.032 mmol) were added. The mixture was stirred at 150 0C for another 10 min under microwave irradiation.Then the mixture was diluted with H20 and extracted with DCM. The organic layer was dried (MgSO4), filtered and the solvent evaporated in vacuo. The crude product was purified by flash column chromatography (silica; EtOAc in Heptane 0/100 to 75/25) and by RP HPLC (Stationary phase: C18 XBridgeTM 30 x 100 mm 5 um, Mobile phase: Gradient from 67% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 33% CH3CN to 50% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 50% CH3CN). The desired fractions were collected and concentrated in vacuo to yield compound 156 (80 mg, 24%) as a solid. 1H NMR (400 MHz, CDC13)0 ppm 0.62 - 0.77 (m, 2 H) 0.91 - 1.06 (m, 2 H) 1.72 (d, J=6.7 Hz, 3 H) 1.91 (tt, J=8.5, 5.1 Hz, 1 H) 2.56 (s, 3 H) 3.93 (dd, , 6.9 Hz, 1 H) 4.25 (dd, , 4.2 Hz, 1 H) 4.75 (quind, J=6.6, 4.4 Hz, 1 H) 7.09 - 7.18 (m, 2 H) 7.18 - 7.25 (m, 2 H) 7.48 (dd, J=5.1, 1.2 Hz, 1 H) 7.53 (s, 1 H) 7.79 (s, 1 H) 8.45 (d, J=5.1 Hz, 1 H) Example 19 (7S)—7-Methyl-3 -(6-piperazinyl-3 -pyridyl)-5 -[4-(trifluoromethyl)phenyl] -6,7- dihydropyrazolo[l,5-a]pyrazinone (E-19, Co. No. 176) roacetic acid (0.911 mL, 11.91 mmol) was added to a stirred solution of intermediate I-42 (663 mg, 1.19 mmol) in DCM (1.9 mL). The mixture was d at rt for 1 h. The solvent was concentrated in vacuo. The crude product was purified by flash column chromatography (silica; MeOH in DCM 0/100 to 20/80). The desired fractions were collected and evaporated in vacuo. The residue was itated with Et20 and filtrated a solid that was purified by RP HPLC (Stationary phase: C18 XBridgeTM 50 X 100 5 um, Mobile phase: Gradient from 53% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 43% CH3CN to 40% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 60% CH3CN), to yield compound 176 (151 mg, 28%) as a solid. 1H NMR (500 MHz, CDC13)5 ppm 1.73 (d, J=6.6 Hz, 3 H) 1.76 (br. s., 1 H) 2.92 - 3.02 (m, 4 H) 3.50 - 3.57 (m, 4 H) 4.00 (dd, J=12.4, 7.2 Hz, 1 H) 4.27 (dd, J=12.4, 4.0 Hz, 1 H) 4.70 - 4.82 (m, 1 H) 6.63 (d, J=8.7 Hz, 1 H) 7.50 (br. d, J=8.7 Hz, 2 H) 7.68 (br. d, J=8.7 Hz, 2 H) 7.71 (s, 1 H) 7.96 (dd, J=9.0, 2.3 Hz, 1 H) 8.42 (d, J=2.3 Hz, 1 H) Example 20 (7S)—7-Methyl-3 thylpyridyl)[6-(trifluoromethyl)pyridyl]-6,7- dihydropyrazolo[l,5-a]pyrazinone (E-20, Co. No. 186) Pd(PPh3)4 (155 mg, 0.134 mmol) was added to a stirred suspension of intermediate I-18 (325 mg, 1.341 mmol), 2-chloro(trifluoromethyl)pyridine (365 mg, 2.012 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (155 mg, 0.268 mmol), CS2C03 (874 mg, 2.683 mmol) in 1,4-dioxane (10 mL) in a sealed tube and under en. The mixture was stirred at 120 0C for 7 h. The mixture was filtered through a pad of diatomaceous earth and washed with DCM. The filtrate was evaporated in vacuo and the crude product was purified by flash column chromatography (silica, EtOAc in DCM 0/100 to 30/70). The desired fractions were collected and concentrated in vacuo.
The residue was purified by ion exchange chromatography using an (ISOLUTE® SCX2 cartridge) eluting first with MeOH then with 7M solution of ammonia in MeOH.
The desired fractions ned in the 7M solution of ammonia in MeOH were collected and the solvents evaporated in vacuo. The residue was triturated with Et20 to yield compound 186 (415 mg, 80%) as a white solid. 1H NMR (500 MHz, 5 , coon) ppm 1.73 (d, J=6.4 Hz, 3 H) 2.60 (s, 3 H) 4.35 - 4.44 (m, 1 H) 4.68 - 4.80 (m, 2 H) 7.41 (dd, J=5.2, 1.2 Hz, 1 H) 7.45 (s, 1 H) 7.78 (s, 1 H) 7.94 (dd, J=8.8, 2.2 Hz, 1 H) 8.24 (d, J=9.0 Hz, 1 H) 8.52 (d, J=5.2 Hz, 1 H) 8.69 - 8.73 (m, 1 H). e 21 (7S)—7-Methyl-3 -(2-methylpyridyl)[6-methyl(trifiuoromethyl)pyridyl]-6,7- dihydropyrazolo[l,5-a]pyrazinone (E-21, Co. No. 192) Tetramethyltin (32 uL, 0.231 mmol) was added to a mixture of intermediate I-43 (65 mg, 0.154 mmol), lithium chloride (13 mg, 0.308 mmol) and bis(triphenylphosphine)palladium(II) ride (6 mg, 0.007 mmol) in degassed DMF (2.4 mL), in a sealed tube under nitrogen. The mixture was stirred at 110 0C for 5 h.
The mixture was diluted with a sat. sol. ofNaHC03 and extracted with EtOAc. The organic layer was separated, dried (Na2SO4), d and the solvents evaporated in vacuo. The crude t was purified by flash column chromatography (silica; EtOAc in DCM 0/100 to 30/70). The desired fractions were collected and concentrated in vacuo. Then the product was triturated with EtZO to yield compound 192 (26 mg, 42%) as a white solid. 1H NMR (400 MHZ, CDClg) 5 ppm 1.73 (d, J=6.5 Hz, 3 H) 2.60 (s, 3 H) 2.69 (br. d, J=1.6 Hz, 3 H) 4.34 - 4.46 (m, 1 H) 4.66 - 4.80 (m, 2 H) 7.41 (dd, J=5.1, 1.2 Hz, 1 H) 7.44 (s, 1 H) 7.78 (s, 1 H) 7.90 (d, J=8.8 Hz, 1 H) 8.02 (d, J=8.6 Hz, 1 H) 8.52 (d, J=4.9 Hz, 1 H).
Example 223 (7S)—5-[6-Ethoxy(trifiuoromethyl)pyridyl]methyl-3 thylpyridyl)-6,7- dihydropyrazolo[1,5-a]pyrazinone (E-22a, Co. No. 189) 2014/061478 EtOH (114 uL, 1.95 mmol) was added to a stirred suspension of sodium hydride (60% dispersion in mineral oil) (78 mg, 1.95 mmol) in DMF (5 mL) at 0 0C. The mixture was stirred at rt for 10 min. Then, a solution of 2-chloroiodo(trifluoromethyl)pyridine (0.5 g, 1.62 mmol) in DMF (5 mL) was added at 0 0C and the mixture was stirred at rt for 18 h. Then, more sodium hydride (60% dispersion in mineral oil) (26 mg, 0.65 mmol) and EtOH (38 uL, 0.65 mmol) were added at 0 0C and the mixture was stirred at rt for 2 h. ediate I-18 (157 mg, 0.65 mmol) was then added and the mixture was cooled to 0 0C. More sodium hydride (60% dispersion in mineral oil) (52 mg, 1.301 mmol) was added and the e was stirred at rt for 1 h and at 80 0C for 16 h. Then more sodium hydride (60% dispersion in mineral oil) (13 mg, 0.325 mmol) was added at rt and the mixture was d at 80 0C for 2 h more. The mixture was treated with a % NH4Cl sol. and extracted with EtOAc/THF. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo. The residue was dissolved in DMF (10 mL). TEA (0.226 mL, 1.626 mmol) and HATU (0.247 g, 0.605 mmol) were added. The mixture was stirred at rt for 1 h. The mixture was treated with a sat. NaHC03 sol./brine at 0 0C and extracted with EtOAc. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo. The crude product was d by flash column chromatography a; EtOAc in DCM 0/100 to 100/0). The desired fractions were collected and concentrated in vacuo. Then the residue was repurified by RP HPLC (Stationary phase: C18 XBridgeTM 30 x 100 mm 5 um, Mobile phase: Gradient from 54% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 46% CH3CN to 64% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 36% CH3CN) to yield compound 189 (27 mg, 4%) as a beige solid. 1H NMR (500 MHz, CDC13)5 ppm 1.46 (t, J=6.9 Hz, 3 H) 1.71 (d, J=6.6 Hz, 3 H) 2.60 (s, 3 H) 4.15 - 4.27 (m, 2 H) 4.39 (dd, J=13.3, 7.2 Hz, 1 H) 4.65 - 4.80 (m, 2 H) 7.40 (dd, J=5.2, 1.2 Hz, 1 H) 7.43 (s, 1 H) 7.77 (s, 1 H) 7.82 (s, 1 H) 8.47 (s, 1 H) 8.52 (d, J=5.2 Hz, 1 H).
Example 22b -[4-Chloro(trifluoromethyl)pyridyl]methyl(2-methylpyridyl)-6,7- dihydropyrazolo[1,5-a]pyrazinone (E-22b, Co. No. 204) Pd(PPh3)4 (47 mg, 0.041 mmol) and 2,4-dichloro(trifluoromethyl)pyridine (134 mg, 0.619 mmol) were added to a stirred suspension of intermediate I-18 (100 mg, 0.413 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (48 mg, 0.082 mmol) and CS2C03 (269 mg, 0.082 mmol) in 1,4-dioxane (2.5 mL) in a sealed tube and under nitrogen. The mixture was stirred at 110 0C for 4 h and at 100 0C for 2 days. The e was filtered h a pad of diatomaceous earth and washed with DCM. The filtrate was evaporated in vacuo. The residue was ved in DMF (7 mL) and TEA (57 uL, 0.413 mmol) then HATU (157 mg, 0.413 mmol) were added. The mixture was stirred at rt for 2 h. The mixture was treated at 0 0C with a sat. sol. NaHC03/brine then EtOAc was added. The mixture was filtered through a pad of diatomaceous earth. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo. The crude product was purified by flash column chromatography (silica; EtOAc in DCM 0/100 to 100/0). The desired fractions were collected and concentrated in vacuo. The residue was repurified by RP HPLC (Stationary phase: C18 XBridgeTM 30 x 100 mm 5 um, Mobile phase: Gradient from 54% 0.1% NH4C03H/NH4OH pH 9 on in Water, 46% CH3CN to 64% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 36% CH3CN) to yield compound 204 (27 mg, 15%) as a white solid. 1H NMR (500 MHz, CDC13)5 ppm 1.72 (d, J=6.4 Hz, 3 H) 2.61 (s, 3 H) 4.36 - 4.45 (m, 1 H) 4.68 - 4.79 (m, 2 H) 7.39 (dd, J=5.2, 1.7 Hz, 1 H) 7.43 (s, 1 H) 7.78 (s, 1 H) 8.42 (s, 1 H) 8.54 (d, J=5.2 Hz, 1 H) 8.68 (s, 1 H).
Example 23 (7S)—3-(2-Iodopyridyl)methyl[4-(trifiuoromethyl)phenyl]-6,7- dihydropyrazolo[l,5-a]pyrazinone (E-23, Co. No. 225) Acetyl de (84 uL, 1.18 mmol) was added to a stirred suspension of intermediate I-26 (320 mg, 0.786 mmol) and NaI (1.18 g, 7.866 mmol) in CH3CN (12.8 mL) at rt.
The mixture was stirred at 120 0C for 30 min under MW ation. Then the mixture was diluted with EtOAc and washed with a sat. sol. ofNa2S203 and brine. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo. The crude product was purified by flash column chromatography (silica; EtOAc in Heptane 0/100 to 60/40). The desired fractions were collected and evaporated in vacuo to yield compound 225 (289 mg, 74%). 1H NMR (400 MHz, CDClg) 8 ppm 1.75 (d, J=6.5 Hz, 3 H) 4.02 (dd, J=12.8, 7.3 Hz, 1 H) 4.30 (dd, J=12.7, 4.2 Hz, 1 H) 4.80 , J=6.7, 4.2 Hz, 1 H) 7.50 (br. d, J=8.3 Hz, 2 H) 7.67 (dd, J=5.1, 1.6 Hz, 1 H) 7.72 (br. d, J=8.3 Hz, 2 H) 7.80 (s, 1 H) 8.03 - 8.05 (m, 1 H) 8.32 (dd, J=5.2, 0.6 Hz, 1 H) e 24 (7S)—7-Methyl-3 -(2-piperazinylpyridyl)[4-(trifluoromethyl)phenyl] -6,7- dihydropyrazolo[1,5-a]pyrazinone hydrochloride salt (E-24, Co. No. 175) .HCl Compound 175 was obtained starting from intermediate I-33a (200 mg, 0.474 mmol), 1- mopyridyl)piperazine (CAS: 12016435, 157 mg, 0.649 mmol, 1.06 mmol), 3)4 (34 mg, 0.029 mmol) in 1,4-dioxane (4 mL) and a sat. sol. ofNa2C03 (2 mL), following a procedure r to that described in E-12, then treatment with a solution of HCl 5N in z'PrOH, yielded compound 175 (224 mg, 84%) as a pale yellow solid. 1H NMR (400 MHz, DMSO-d6) 8 ppm 1.59 (d, J=6.5 Hz, 3 H) 3.22 (br. s., 4 H) 3.83 (br. s., 4 H) 4.10 (dd, J=12.9, 7.4 Hz, 1 H) 4.39 (dd, J=12.9, 4.2 Hz, 1 H) 4.81 - 4.92 (m, 1 H) 7.29 (br. d, J=4.4 Hz, 1 H) 7.56 (br. s., 1 H) 7.69 (br. d, J=8.6 Hz, 2 H) 7.84 (br. d, J=8.6 Hz, 2 H) 8.11 (d, J=5.8 Hz, 1 H) 8.19 (br. s, 1 H) 9.20 (br. s., 2 H).
Example 25 (7S)—3 -[2-(4-Acetylpiperazinyl)pyridyl] methyl-5 -[4-(trifluoromethyl)phenyl] - 6,7-dihydropyrazolo[1,5-a]pyrazinone (E-25, Co. No. 106) —124— Acetyl chloride (4 uL, 0.060 mmol) was added to a solution of compound 175 (25 mg, 0.054 mmol) and TEA (16 uL, 0.115 mmol) in DCM (1 mL) under nitrogen. The mixture was stirred at rt for 5 h. Then the mixture was diluted with HCl 0.1N and extracted with DCM. The organic layer was separated, dried (MgSO4), d and the solvent evaporated in vacuo. The crude product was purified by flash column chromatography a; MeOH in DCM 0/100 to 05/95). The desired fractions were collected and concentrated in vacuo to yield compound 106 (17 mg, 62%) as a solid. 1H NMR (400 MHz,CDC13)8 ppm 1.75 (d, J=6.5 Hz, 3 H) 2.13 (s, 3 H) 3.49 - 3.55 (m, 2 H) 3.55 - 3.61 (m, 2 H) 3.61 - 3.67 (m, 2 H) 3.70 - 3.77 (m, 2 H) 4.01 (dd, J=12.7, 6.9 Hz, 1 H) 4.30 (dd, J=12.7, 4.2 Hz, 1 H) 4.79 (quind, J=6.6, 4.4 Hz, 1 H) 6.94 (dd, J=5.2, 1.3 Hz, 1 H) 7.17 (br. s, 1 H) 7.46 - 7.55 (m, 2 H) 7.66 - 7.76 (m, 2 H) 7.80 (s, 1 H) 8.19 (dd, J=5.2, 0.6 Hz, 1 H). e 26 7-(Difluoromethyl)-3 -(2-methylpyridyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[l,5-a]pyrazinone (E-26, Co. No. 181) F F Compound 181 was obtained starting from intermediate I-46 (71 mg, 0.169 mmol) using Pd/C 10% (36 mg, 0.033 mmol) in EtOH (3 mL) under H2 atmospheric pressure, following a procedure similar to that bed in E-6, yielding compound 181 (13 mg, 19%) as a white solid. 1H NMR (400 MHz, CDClg) 5 ppm 2.58 (s, 3 H) 4.36 (dd, J=13.6, 3.2 Hz, 1 H) 4.61 (ddd,.]=13.6, 5.0, 1.3 Hz, 1 H) 4.88 - 4.99 (m, 1 H) 6.21 - 6.55 (m, 1 H) 7.45 (dd, J=5.2, 1.3 Hz, 1 H) 7.47 - 7.54 (m, 3 H) 7.73 (br. d, J=8.3 Hz, 2 H) 7.89 (s, 1 H) 8.50 (d, J=5.1 Hz, 1 H).
Example 27 (7S)—7-Methyl[2-(methylamino)pyridyl][4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[1,5-a]pyrazinone (E-27, Co. No. 147) 8 K("‘N/ Compound 147 was obtained ng from ediate I-33a (1.5 g, 3.561 mol), 4- N—methyl-pyridinamine (799 mg, 4.273 mmol, 1.06 mmol), Pd(PPh3)4 (206 mg, 0.178 mmol) in 1,4-dioxane (8.1 mL) and a sat. sol. ofNa2C03 (8.2 mL), following a procedure similar to that described in E-12, yielding compound 147 (1.14 g, 80%) as a white solid. 1H NMR (500 MHz, CDClg) 5 ppm 1.74 (d, J=6.4 Hz, 3 H) 2.93 (d, J=5.2 Hz, 3 H) 4.00 (dd, J=12.6, 7.1 Hz, 1 H) 4.29 (dd, , 4.0 Hz, 1 H) 4.54 (br. d, J=3.2 Hz, 1 H) 4.73 - 4.82 (m, 1 H) 6.84 (s, 1 H) 6.86 (d, J=5.2 Hz, 1 H) 7.50 (br. d, J=8.4 Hz, 2 H) 7.70 (br. d, J=8.4 Hz, 2 H) 7.79 (s, 1 H) 8.09 (d, J=5.2 Hz, 1 H).
Example 28 (7S)—5-[4-Iodo(trifluoromethyl)—2-pyridyl]methyl-3 -(2-methylpyridyl)-6,7- dihydropyrazolo[1,5-a]pyrazinone (E-28, Co. No. 212) Intermediate I-18 (320 mg, 1.32 mmol) was added portionwise to a stirred suspension of sodium hydride (60% dispersion in mineral oil, 78 mg, 1.98 mmol) in DMF (5 mL) at rt. The mixture was stirred at rt for 15 min and a solution of 2-chloroiodo (trifluoromethyl)pyridine (446 mg, 1.453 mmol) in DMF (5 mL) was added at rt. The mixture was stirred at 80 0C for 16 h. Then more sodium hydride (60% dispersion in mineral oil, 27 mg, 0.66 mmol) was added at rt and the mixture was stirred at 80 0C for 1 h. The mixture was treated with 10% NH4Cl sol/brine and extracted with EtOAc.
The organic layer was separated, washed with brine, dried (Na2SO4), filtered and the ts evaporated in vacuo. The crude product was purified by flash column tography (silica; EtOAc in DCM 0/100 to 100/0). The desired fractions were collected and the solvents concentrated in vacuo to yield compound 212 (220 mg, 32%) as a white foam. -l26- Example 29 -(3,4-Dichloroiodo-phenyl)methyl(2-methylpyridyl)-6,7- dihydropyrazolo[1,5-a]pyrazinone (Co. No. 220) and (7S)—5 -(3,4-dichloroiodo methyl-cyclohexa- l ,3 ,5 -trien- l -yl)methyl-3 -(2-methylpyridyl)-6,7- dihydropyrazolo[l,5-a]pyrazinone (Co. No. 221) (E-29, Co. No. 220 and Co. No. 221) 220 221 HATU (89 mg, 0.235 mmol) was added to a d solution of mixture intermediate compounds I-63a and I-63b (250 mg, 0.235 mmol) and TEA (65 uL, 0.471 mmol) in DMF (3 mL). The mixture was stirred at rt for 2 h. The mixture was treated with a sat. sol. of NH4Cl and a sat. sol. ofNaHC03 and extracted with EtOAc. The organic layer was separated, dried (MgSO4), filtered and the solvents evaporated in vacuo. The crude product was purified by flash column tography (silica; EtOAc in e 0/100 to 90/10). The desired fractions were collected and the solvents concentrated in vacuo to give two fractions that were triturated with DCM/Heptane to yield compound 220 (55 mg, 45%) and compound 221 (20 mg, 16%) as solids. nd 220: 1H NMR (500 MHz,CDC13)8 ppm 1.78 (d, J=6.4 Hz, 2 H) 1.85 (d, J=6.6 Hz, 1 H) 2.58 (s, 3 H) 3.82 (dd, J=12.7, 9.2 Hz, 0.65 H) 3.97 (dd, J=12.7, 7.2 Hz, 0.35 H) 4.00 - 4.07 (m, 1 H) 4.76 - 4.84 (m, 0.35 H) 4.92 - 5.00 (m, 0.65 H) 7.39 (s, 0.35 H) 7.40 (s, 0.65 H) 7.48 (br. d, J=5.2 Hz, 1 H) 7.52 - 7.56 (m, 1 H) 7.82 (s, 1 H) 8.03 (s, 0.35 H) 8.03 (s, 0.65 H) 8.48 (d, J=5.2 Hz, 1 H); compound 221: 1H NMR (500 MHz, CDClg) 5 ppm 1.78 (d, J=6.6 Hz, 2 H) 1.85 (d, J=6.6 Hz, 1 H) 2.57 (s, 3 H) 3.81 (dd, J=12.7, 9.0 Hz, 0.65 H) 3.98 (dd, J=12.7, 4.6 Hz, 0.35 H) 4.02 - 4.11 (m, 1 H) 4.76 - 4.84 (m, 0.35 H) 4.95 - 5.04 (m, 0.65 H) 7.16 (d, J=8.7 Hz, 0.35 H) 7.17 (d, J=8.7 Hz, 0.65 H) 7.49 (br. d, J=5.2 Hz, 1 H) 7.52 - 7.61 (m, 2 H) 7.83 (s, 0.65 H) 7.83 (s, 0.35 H) 8.47 (d, J=5.2 Hz, 1 H).
The following final nds were synthesized by following an analogous synthetic procedure as reported for compound 1 (E-l) followed by the procedure for intermediates I-18 and I-19 when needed. 2014/061478 Structure Com ound number Startin_ material -l28- n material Co. No. 121 The following compound was sized by following the sequence of an analogous synthetic procedure as reported for intermediate I-22 starting from intermediate I-14 and l-bromo-3,4-dichlorobenzene, followed by the procedure for intermediates I-23 then following an analogous synthetic procedure as ed for compound 2 (E-2) using 2-meth l 4,4,5,5-tetrameth l-l,3,2-dioxaborolan l o ridine.
Structure Intermediate number Starting material Co. No. 6a Example 30 3-(2-Methylpyridyl)(trifluoromethyl)[4-(trifluoromethyl)phenyl]-6,7- dihydropyrazolo[l,5-a]pyrazinone (Co. No. 238) WN‘N/ Compound 238 (E-30) was ed starting from intermediate I-68 (20 mg, 0.042 mmol), 2-picolineboronic acid (8 mg, 0.059 mmol), Pd(PPh3)4 (2 mg, 0.002 mmol) in l,4-dioxane (0.4 mL) and a sat. sol. ofNaHC03 (0.4 mL) following a procedure similar to that described in E-12 and purified by RP HPLC ((Stationary phase: C18 XBridge 30 X 100 5 um), e phase: Gradient from 60% 0.1% NH4C03H/NH4OH pH 9 solution in Water, 40% CH3CN to 43% 0. l% NH4C03H/NH4OH pH 9 on in Water, 57% CH3CN)), yielding compound 238 (14 mg, 75%). 1H NMR (500 MHz, CDC13)5 ppm 2.53 (s, 3 H) 4.23 (dd, J=l4.0, 1.3 Hz, 1 H) 4.67 - 4.74 (m, l H) 5.07 - 5.14 (m, l H) 7.38 - 7.43 (m, 3 H) 7.47 (s, l H) 7.67 (br. d, J=8.4 Hz, 2 H) 7.87 (s, l H) 8.44 (d, J=5.2 Hz, 1 H).
Tables la (compounds 1-87) and lb (with an alternative representation for nds 1-87) below list additional compounds of a (1).
Tables 1a and 1b. The following compounds were prepared following the methods exemplified in the Experimental Part (Ex. No.). Compounds exemplified and described in the experimental part are marked with an asterisk *. The work-up for compounds synthesized by an analogous ure to El can be performed either by filtration through a pad of diatomaceous earth or by extraction with an organic solvent, washing with aqueous ammonia. The coupling agent used in the synthesis of compounds synthesized by an analogous procedure to E2 was either a boronic acid or a boronic ester. For some nds the stereochemical configuration has been designated as *R or *8 when the absolute chemistry is undetermined although the compound itself has been isolated as a single stereoisomer and is enantiomerically pure.
Table 1a 0 R2 R\NM R3 R4 Co. Salt form 1 2 4 3 Ex. No. R R R R 1a .HCl 1b .HZSO4 1c E1* -Me (S) -H .CH3SO3H .HOzCC 1d H=CHC OzH-cz's 2 E2* -Me (S) -H 3 E1 -Me (S) -H 4 E1 -Me (S) -H WO 95311 C0. Salt form R R3 -Me (S) -H . HCl 6 -Me (S) -H . HCl 6a -Me (S) -H 7 -Me (S) -H 8 -Me (S) -H 9 -Me (S) -H -H 11 -Me -H 12 -Me (S) -H . HCl 13 -Me (S) -H 14 -Me (S) -H -Me (S) -H . HCl 16 -Me (S) -H WO 95311 — 131 — X. 0.
E1 -Me (S) -H . HCl 21 E1 6:: -Me (S) -H 22 E2 'QCFs -Me (S) -H . HCl 23 E1 "C; -Me (S) -H 24 E2 "W -Me (S) -H E1 "@FFg -Me (S) -H . HCl 26 E1 -Me (R) -H 27 E1 -Me (S) -H 23 E1 _ _ <: CH(CH3) E1 11 E1 Q CH(CH3) CH CH( 3) 12 E1 .HCl CF3 (S) 13 E1 @"3 CH(CH3) 14 E2 @ CH CH( 3) E1 .HCl CH(CH3) 16 E1 CH CH( 3) 17 E1 .HCl CH(CH3) 18 E1 CH(CH3) 19 E1 CH CH( 3) E1 .HCl CH(CH3) 21 E1 CH CH( 3) 22 E2 .HCl WO 95311 —139— N0. N0.
CH(CH3) CH(CH3) CH CH ((8) 3) .HC1 CH(CH3) CH(CH3) CH CH( 3) 28 .HC1 CH(CH3) CH(CH3) _ CH(CH3) 31 E1 "@CF3 " \ /N (R) "@CFs _N CH CH 32 E2 " \ / ((3) 33 E1 "@0F3 __ CH2 \ /N _ CH CH( 3) 34 E1 -- OMe __ \ N / (S) -- OMe _ CH CH( 3) E1 Q .HC1 __ \ N / (S) — 140 — C0. EX. Salt form 3 4 CR R N0 N0 CH(CH3) 37 E2 CH CH( 3) 38 E1 .HCl 39 E1 CH2 CH(CH3) 41 E1 42 E1 CH(CH3) 44 E4* CH(CH3) CH(CH3) 45 E5* CH(CH3) 46 E6* CH(CH3) 47 E1 __ CI (S) o_\— 48 E1 CH(CH3) " CFs " \ )N (S) W0 2014/195311 C0. EX. Salt form CR3R4 N0. N0.
CH(CH3) 49 E1 50 E1 CH(CH3) 51 E1 52 E8* CH(CH2F) CH(CH3) 53 E1 CH(CH3) 54 E1 CH(CH3) 55 E1 CH(CH3) 56 E1 CH(CH3) 57 E1 CH 58 E1 . HC1 CH(CH3) 59 E1 CH(CH3) 60 E1 C0. Salt form CR3R4 CH(CH3) CH(CH3) 63 .HC1 CH(CH3) CH 65 .HC1 CH(CH3) 66 .HC1 CH(CH3) CH(CH3) CH(CH3) 69 .HC1 70 E1 '< >—CF3 __ \— N CH(CH2CH3) " \ /N (S) WO 95311 C0. EX. Salt form 3 4 CR R N0 N0 72 E1 _ _ CH(CH3) 74 @CF CH(CH20H) CH(CH3) 75 E1 _ _ (S) CH(CH3) 76 E1 _ _ (S) CH(CH3) 77 1310* __ CH(CH3) 78 E1 CH 79 E1 .HCl CH(CH3) 80 E1 81 E11* CH(CH3) .HCl CH(CH3) 82 E1 CH(CH3) 83 E1 — 144 — C0. Salt form 3 4 CR R CH(CH3) CH(CH3) 85 __ 86 Q ) 87 @ CH(CH20H) CH(CH3) 88 E3 89 E3 "QCI — CH(CH3) \ /N (S) CI \N_ CH(CH2F) 90 E8 _ \ /N (*R) CI \N_ CH(CH2F) 91 E8 _ __ \ /N (*S) C' d 92 E13 N CH(CH3) CF3 — (S) " \ /N CI HN— 93 E8 — CI __ CH(CH2F) \ N 94 E13 -@CF3 Nrj CH(CH3) — (S) " \ /N WO 95311 —145— C0. EX. Salt form 1 2 3 4 R R CR R N0. N0.
CH(CH3) 95 E13 CH(CH3) 96 E1 CH(CH3) 97 E13 CH(CH3) 98 E8 CH(CH3) 99 E13 CH(CH3) 100 E13 CH(CH3) 101 E12 CH(CH3) 102 E12 CH CH( 3) 103 E3 CH CH( 3) 104 E3 CH(CH3) 105 E12 W0 95311 — 146 - C0. Salt form 3 4 CR R CH CH( 3) CH CH( s) 107 ,HCl CH CH( 3) CH CH( 3) CH CH( 3) CH CH( 3) CH CH( 3) CH CH( 3) 113 ©—< CH CH( 3) CH CH F( 2 ) (*5) —147- C0. EX. Salt form N0. No.
CH(CH2F) 116 IE8 "Q7 "CF (*R) CH(CH3) 117 E8 '_\)N (S) 118 IE1 "Q7 "C CH(CH20Me) (*S) CH(CH20Me) 119 IE1 "67 - ---<\:// .2HC1 -\—/N CH(CH3) 123 E2 __@CF3 ---\_E _\/N (S) CH(CH3) 124 E13 ----\ /N (S) 125 E14* CH(CH3) 0' \ )N (S) 126 E13* '-Q CH(CH3) N (S) * __ "CNN CH(CH3) 127 E12 @Cfi (S) C0. EX. Salt form 3 4 N0 N0 CH(CH3) 128 E14 CH(CH2CH3) 129 E1 CH(CH2CH3) 130 E1 CH(CH3) 131 E8 CH(CH3) 132 E1 CH CH( 3) 133 E2 .HC1 CH(CH3) 134 E6 135 E17 CH(CH3) 136 E1 CH CH( 3) 137 E2 .HC1 CH CH( 3) 138 E2 .HC1 CH(CH3) 139 E1 —149— CH CH( 3) CH CH( 3) CH CH( 3) 143 CH(CH20Me) 144 CH(CH20Me) CH CH( 3) CH CH( 3) CH CH( 3) CH CH( 3) > _ 149 E17* "©—< __ N OH \ / (S) ""QCFg, — / 0 CH 150 E3 \ / N (S) E2 ""@CF3 \ / CN CH(CH3) N (S) CH(CH3) — 152 E1 WQOCQ __ \ N / (S) N0. N0.
CH CH 153 "@Ca ((5) 3) 0% CH(CH3) 154 ----@CF3 (S) CH(CH3) 155 "Goa (S) CH(CH3) 156 < >—< (S) 157 H3) 158 CHESC)H3) 159 CHESC)H3) 160 CHESC)H3) 161 CHESC)H3) 162 CHESC)H3) 163 CHESC)H3) 164 CHESC)H3) 2014/061478 CH(CH3) CH(CH3) CH(CH3) CH(CH3) CH(CH3) CH(CH3) 171 C(CH3)2 CH(CH3) CH 173 . HCl CH(CH3) 174 __ CH 175 . HCl CH(CH3) W0 95311 C0. EX. Salt form 3 4 CR R N0. N0.
CH(CH3) 177 E10 CH CH CH CH CH CH 181 "Q CH(CHF2) CH CH( 3) "3 (S) CH CH( 3) "3 (S) CH CH F( 2 ) CI (*R) CH CH F( 2 ) (*8) CH CH( 3) CH CH( 3) 187 CI CH CH( 3) CF3 (S) / CFs CH CH( 3) O—\ (S) WO 95311 Salt form WO 95311 —154— Salt form 3 4 CR R CH(CH3) CH(CH3) CH(CH3) CH(CH3) CH(CH3) CH(CH3) CH(CH3) CH(CH3) CH(CH3) 211 E1 ----\ / CF3 CH2 CH(CH3) CH(CH3) 213 E28 ____\ / wo 2014/195311 C0. EX. Salt form 3 4 N0 N0 CH(CH3) 214 E13 I-26* CH(CH3) E3 (S) 216 E1 SL4? I’ OH \ H 217 E1 *S CH CH 219 E2 CH(CH20H) CH(CH3) 220 E29* CH(CH3) 221 E29* 222 F) CH CH 224 CH(CH20H) CH(CH3) 225 E23* CH CH OH (*S) 2014/061478 C0. Salt form 3 4 CR R CH CH CH( 2 ) (*R) CH CH( 3) CH CH( 3) CH CH( 3) CH CH CH( 2 ) (*5) CH CH CH( 2 ) (*R) 233 CH(CH20H) CH CH( 3) CH CH( 3) CH CH( 3) 236 ,HCl CH CH( 3) 238 CH(CF3) WO 95311 — 157 — CH CH( 3) CH CH( 3) CH CH( 3) CH CH( 3) CH CH( 3) 244 CH2 CH CH( 3) CH CH( 3) CH CH( 3) CH CH( 3) CH CH( 3) WO 95311 C0. EX Salt form N0. N0 250 E20 251 E12 252 E16 253 E13 254 E4 255 E13 256 E12 257 E13 258 E12 259 E13 260 E12 261 E12 C0. Salt form 3 4 CR R CH(CH3) CH(CH3) CH(CH3) CH(CH3) CH(CH3) CH(CH3) The values of salt stoichiometry or acid content in the nds as provided , are those obtained experimentally and may vary when using ent ical methods. The content of hydrochloric acid reported herein was determined by 1H NMR integration and/or elemental analysis. For compound 1 the salt stoichiometry was ined by ion chromatography (hydrochloride and sulfate salts) and by NMR (methanesulfonate and maleate salts).
Analytical part Melting points Values are peak values, and are obtained with experimental uncertainties that are commonly ated with this analytical method.
Mettler PF 62 1A): For a number of compounds, melting points were determined in open capillary tubes on a Mettler FP62 apparatus. Melting points were measured with a temperature gradient of 3 or 10 oC/minute. Maximum temperature was 300 oC. The melting point was read from a digital display. 2014/061478 -l60- Mettler PF 62 (Al 1: Melting points (m.p.) were determined in open capillary tubes on a Mettler FP62 apparatus. Melting points were measured with a temperature ranging from 50°C to 300°C a gradient of 10 oC/minute. The melting point value was , using read from a digital display.
Mettler FP 81HT / FP90 1B 1: For a number of compounds, melting points were determined in open capillary tubes on a PP 81HT / FP90 apparatus (Mettler-Toledo).
Melting points were measured with a temperature gradient of l, 3, 5 or 10 C’C/minute.
Maximum temperature was 300 CC. The melting point was read from a l display.
Mettler Toledo MP50 1C 1: For a number of compounds, melting points were determined in open capillary tubes on a Mettler Toledo MP50. Melting points were measured with a temperature gradient of 10 0C/minute. Maximum temperature was 300 0C. The melting point data was read from a l display and checked from a video recording system.
DSC823e 1D 1: For a number of compounds, g points (m.p.) were determined with a DSC823e (Mettler-Toledo). Melting points were ed with a temperature gradient of 30 oC/minute. Maximum temperature was 400 oC. Peak values were recorded.
LCMS l grocedure The High Performance Liquid Chromatography (HPLC) measurement was performed using a LC pump, a array (DAD) or a UV detector and a column as specified in the respective methods. If necessary, additional detectors were included (see table of methods .
Flow from the column was brought to the Mass Spectrometer (MS) which was configured with an atmospheric pressure ion source. It is within the knowledge of the d person to set the tune parameters (e.g. scanning range, dwell time...) in order to obtain ions allowing the identification of the compound’s nominal otopic molecular weight (MW). Data acquisition was performed with appropriate software.
Compounds are described by their experimental ion times (R) and ions. If not specified differently in the table of data, the reported molecular ion corresponds to the [M--H]+ (protonated molecule) and/or [M-H]' tonated molecule). In case the compound was not directly ionizable the type of adduct is specified (i.e. [M+NH4]+, [M--HCOO]', [M+CH3COO]' etc. . .). For molecules with multiple isotopic patterns (Br, Cl..), the reported value is the one obtained for the lowest isotope mass. All s were obtained with experimental uncertainties that are commonly associated with the method used. - l6l - after, "LCT" means LC-Time of , "SQD" Single Quadrupole Detector, "MSD" Mass Selective Detector, "QTOF" Quadrupole-Time of Flight, "RT" room temperature, "BEH" bridged ethylsiloxane/silica hybrid, "DAD" Diode Array Detector.
Table 2. LC-MS Methods (Flow expressed in ; column temperature (T) in CC; Run time in minutes . ment Mobile phase Gradient : Agilent: A: 95% Acquity® From 95% A Eclipse Plus CH3COONH4 UPLC® — to 5% A in C18 RRHD 6.5mM + 4.6min, held DAD and (1.8um, 5% CH3CN, for 0.4min SQD 2. lx50mm) B: CH3CN 95% A kept for 0.2 min, A' 95W. 0 Agilent: to 0% A in Agflent'. _ CH3COONH4 HPl 100— 2.8min, held Eclipse Plus 6.5mM + DAD, for 0.15min, Waters: C2118£33623, B? l/jlcéllilcgl’fl/ back to 95% SQD ' ' 3 A in 0.15min, CH3OH held for l.7min From 95% A Agilent YMC-pack A: 0.1% to 5% A in 1100 - ODS-AQ HCOOH in 4.8 min, held DAD-MSD C18 (50 x 4.6 H20 for 1.0 min, Gl956A mm, 3 um) B: CH3C\I to 95% A in 0.2 min.
A: 95% . Agilent: ' From 95% A Eclipse Plus CH3COOI\H4 Acquit ® to 5% A in C18 RRHD 6'5mM __ UPLC — 1.8min, held (1.8um, 5% CH3C\I, DAD/SQD for 0.2mm. 2‘ 1X50mm) B: CH3C\I A' 95 A). 0 Waters: Waters: From 95% A Acquity® CSHTM C18 "£3533?" to 5% A in UPLC® - (l .7um, ' 0 4.6min, held DAD/SQD 2.1X50mm) 51;) SIZES?) for 0.4min l62- Method Instrument Mobile phase Gradient 95% A for 0.2 min, to A: 95% 0% A in Agilent: Agilent: CH3COONH4 2.8mm, held HP 1 100- Eclipse Plus 6.5mM + 5% for 0. 15min, DAD, MSD C l 8 (3 .5 gm, CH3CN, back to 95% Gl956B 2. 1X30mm) B: CH3CN A in 0. 15min, held for l.7min From 95% A A: 95% Waters: : to 40% A in CH3COONH4 Acquity® CSHTM C l 8 l.2min, to 6.5mM + 5% UPLC® - (1.70m, 5% A in CH3CN, B: DAD/ SQD 2. lx50mm) 0.6mm, held CH3CN for 0.2min 84.2% A for 0.49min, to A: 95% 10.5% A in Waters: BEH CH3COONH4 2. l 8min, held C18 (1 .7nm, 7mM / 5% for 1.94min, 2.1x100mm) CH3CN, back to B: CH3CN 84.2% A in n, held for 0.73min.
From 95% A A: 95% to 0% A in Agilent: Agilent: CH3COONH4 50min, held HPl 100- Eclipse Plus 6.5mM + 5% for 0. 15min, DAD, Cl 8 (3 .5 gm, CH3CN, B: back to 95% 2. 1X30mm) CH3CN/CH30 A in 0. 15min, H, l/l held for l .7min -l63- Instrument Mobile phase Gradient From 95% A A: 95% to 0% A in Agilent: CH3COONH4 Agilent: 5.0mm, held HP 1 100- 6.5mM + 5% Eclipse Plus for 0.15min, DAD, CH3CN, Cl 8 (3 .5 gm, back to 95% Waters: B: 2. 1X30mm) A in 0.15min, SQD CH30 held for H, 1/1 l.7min From 95% A Agilent: A: 95% Waters: to 40% A in Eclipse Plus CH3COONH4 Acquity® l.2min, to Cl 8 RRHD 6.5mM + 5% UPLC® - 5% A in (l .8 gm, CH3CN, B: D 0.6mm, held 2. ) CH3CN for 0.2mm From 95% A Waters: A: 95% Waters: to 40% A in Acquity® CH3COONH4 CSHTM C l 8 l.2min, to UPLC® - 6.5mM + 5% (l .7nm, 5% A in DAD / CH3CN, B: 2. lx50mm) 0.6mm, held QTOF G2-S CH3CN for 0.2mm Waters: A: 95% Waters: From 95% A Acquity® CH3COONH4 CSHTM C l 8 to 5% A in UPLC® - 6.5mM + 5% (l.7nm, 4.6mm, held DAD / CH3CN, B: 2.lx50mm) for 0.4mm QTOF G2-S CH3CN — 164 — Table 3a. Analytical data — melting point (M.p.) and LCMS: [M+H]+ means the protonated mass of the free base of the compound, [M-H]' means the onated mass of the free base of the compound or the type of adduct specified [M+CH3COO]'). Rt means retention time in min . For some comounds, exact mass was ined.
[M-H] or adduct_ 1 -CH3COO ' 2 181.9 (A) -CH3COO)' 1 3 103.3 (B) -CH3COO)' 1 4 247.0 (A) -CH3COO)' 1 >300 (A) -CH3COO)' 1 6 >300 (A) -CH3COO)' 1 7 126.7 (B) -CH3COO)' 1 8 ' 1 9 1 1 11 1 12 1 13 1 14 201.1 (B) O)' 1 >300 (A) -CH3COO)' 1 17 >300 (B) -CH3COO)' 1 18 98.5 (B) -CH3COO)' 1 19 137 (B) -CH3COO)' 1 293.6 (B) -CH3COO)' 1 21 ' 1 22 1 23 1 24 1 26 2 27 1 29 140.8 (B) 401 459 (\/I--CH3COO)' 2.41 1 78.6 (B) 371 429 (\/I--CH3COO)' 2.07 1 31 112.8 (B) 431 489 (\/I--CH3COO)' 2.49 1 32 n.d. 373 431 (\/I--CH3COO)' 2.05 1 33 162.8 (B) 417 475 (\/I--CH3COO)' 2.26 1 2014/061478 [M-H] or adduct 34 -CH3COO 36 1282 (B) -CH3COO) 1 37 254.0 (B) -CH3COO) 1 38 294.0 (B) -CH3COO)' 1 39 185.2 (B) -CH3COO)' 1 40 137.0 (B) -CH3COO)' 1 41 166. 9 (B) -CH3COO)' 1 43 \/1--CH3COO) 1 44 > 300 B 5 45 143. 9 A1 1 46 124.6 B 1 47 185.6 B 5 49 183.9 B 1 50 146. 8 (B) -CH3COO) 5 51 93 (B) -CH3COO) 1 52 >300 (B) O)' 5 53 233.1 (B) -CH3COO)' 5 54 205.1 (B) -CH3COO)' 5 55 104.2 (B) -CH3COO)' 5 56 ' 5 57 5 59 5 60 5 61 5 62 1 64 273.9 (B) -CH3COO)' 5 68 >300 (B) -CH3COO)' 5 70 n.d. -CH3COO)' 5 71 218.9 (B) -CH3COO)' 1 72 88 (B) -CH3COO)' 1 73 144.3 (B) -CH3COO)' 5 74 1 [M-H] or adduct_ 60. 8 (A, 77 Temp. grad; 507 (M+CH3COO)' 3 C’C/rnin 157.75 c’C 88 O)' 92 n.d. -CH3COO)' 93 n.d. -CH3COO)' 94 n.d. -CH3COO)' 210.61 c’C 95 -CH3COO)' 97 n. d. 5 99 126.4 °C B VI-CHgCOO)' 5 100 144. 9 CC B CH3COO 2. 56 5 101 >300 c’C B \/I2--CH3COO 1. 91 5 102 129. 8 CC B 6\/I--CH3COO 2. 33 5 103 164. 7 CC B 4\/I--CH3COO 2.25 5 104 183 CC B 5\/I--CH3COO 2. 66 5 105 124 °C (B) -CH3COO) 5 106 n.d. -CH3COO) 5 107 294 °C (B) -CH3COO)' 5 108 128.1 0C (B) -CH3COO)' 5 109 149.8 °C (B) -CH3COO)' 5 110 2579 °C (B) 5 111 VI-CH3COO)' 5 113 nd 3:\/1——CH3C00 229 11 116 3COO 279 8 118 n.d. 417 475 \/I--CH3COO 2.87 8 119 n.d. 417 475 (\/I--CH3COO)' 2.87 8 120 n.d. 417 475 (\/I--CH3COO)' 2.78 8 121 n.d. 417 475 (\/I--CH3COO)' 2.78 8 122 n.d. 413 471 (\/I--CH3COO)' 2.55 5 123 189.5 °C (B) 417 475 (\/I--CH3COO)' 3.92 10 2014/061478 C0. LCMS M.p. (°C) [M+H]+ [M-H] or adduct N0. Method 105.4 (A, 125 temp. grad: -CH3COO)' 3 C’C/rnin) 126 70.5 °C (B) -CH3COO)' 5 127 155.1 °C (B) -CH3COO)' 5 128 139.8 °C (B) -CH3COO)' 5 129 135.1 °C (B) -CH3COO)' 8 130 134.4 °C (B) VI-CHgCOO)" 8 131 134. 7 °C B ' 5 132 148 °C B 1\/I--CH3COO 2. 33 5 133 191. 5 °C B 5\/I--CH3COO 2. 70 5 134 n. d. 9\/I--CH3COO 2.40 5 135 76. 8 °C B 1\/I--CH3COO 1. 76 5 136 126.2 °C B CH3COO 2. 38 5 137 193. 8 °C (B) -CH3COO) 5 138 173.9 °C (B) -CH3COO) 5 140 231.5 °C (B) -CH3COO)' 5 143 >300 °C (B) -CH3COO)' 5 144 133.2 °C (B) O)' 5 145 57. 5 °C (B) VI-CHgCOO)" 5 146 166. 8 °C B ' 5 147 85.9 °C B 0\/I--CH3COO 2. 01 5 150 >300 °C B 1\/I--CH3COO 2. 39 5 151 157. 6 °C B 6\/I--CH3COO 2.28 5 152 105.4 °C B 1\/I--CH3COO 2.13 5 153 162 °C B 5\/I--CH3COO 2.15 5 154 1695 °C (B) -CH3COO) 155 101.8 °C (B) -CH3COO) 157 158.9 °C (B) -CH3COO)' 158 48.2 0c (B) -CH3COO)' 159 71.5 °C (B) -CH3COO)' 160 1295 °C (B) -CH3COO)' 162 185.9 c’C B [M-H] or adduct 163 n. (1. 477 OO 170.3 0C (A, 164 temp. grad: 389 3 C’C/rnin) 165 n.d. 489 (V1—-CH3COO)' 166 99.8 °C (B) 474 (V1--CH3COO)' 168 108.5 °C (B) 417 169 64.7 °C (B) 495 (V1—-CH3COO)' 171 158 8 °Cd(B) VI--CH3COO)' 174 127.5 °C B M--CH3COO 2.12 01010101010101 175 220. 8 CC B 5\/1--CH3COO 1. 70 U‘I 176 >300 °C B 5\/1--CH3COO 1. 78 179 n..d M--CH3COO 1.93 180 768°C A M--CH3COO 2.41 181 49811(M+CH3C00) 182 67.8 °C (B) 478 (V1—-CH3COO) 183 125.6 °C (B) 490 (V1—-CH3COO)' 184 n.d. 478 (V1—-CH3COO)' 185 n.d. 478 (V1—-CH3COO)' 188 1614 0C (B) 48090(V1—-CH3COO)' 189 142.4°C B 200 122.3 0C A 3COO 2.81 Hmmoooommmmmm 201 119. 7 °C B 6\/I--CH3COO 2.44 U‘I 204 292. 8 °C B 0\/1--CH3COO 2. 51 205 1792°C B 4".-CH3COO 277 207 1476°C B 6".-CH3COO 244 010101 208 1413°C (B) 4767(VI--CH3COO) U‘I 125.66 °C 210 461 (V1--CH3COO)' U‘I 214 n.d. 476 (V1—-CH3COO)' 216 n.d. 415 217 255.5 °C (B) 415 219 n.d. 401 Co. LCMS M660 [M+H]+ [M-H]' or adduct R No. Method 220 n.d. 513 572 M--CH3COO ' 2.48 5 222 >300 °C (B) 405 463 (M--CH3COO) 5 225 n.d. 499 557 (M--CH3COO)' 7 226 n.d. 407 405 7 227 n.d. 407 405 7 229 n.d. 465 523 (M--CH3COO)' 5 235 93 (B) 470 528 (M--CH3COO)' 5 236 491 5 237 125.82 D 433 431 2.34 5 238 n.d. 439.0995 2.32 13 240 107.87 D 434 492 M--CH3COO ' 2.73 5 241 d. 4 16 474 M--CH3COO ' n. 2.04 5 248 n.d. 416 474 COO ' 1.35 7 249 n.d. 478.1874 2.47 13 n.d. = not determined Table 3b. Analytical data — melting point (M.p.) and LCMS: [M+H]+ means the protonated mass of the free base of the compound, Rt means retention time (in min), method refers to the method used for LCMS. 0" LCMS M.p. (°C) [M+H]+ Rt N0. Method 16 174.0 (A) 353 2.00 1 >300 (A) 355 1.87 1 28 >300 (A) 337 1.74 1 >300 A 367 1.79 1 377 1.71 1 48 75.2 A 449 2.27 1 403 2.51 3 371 2.369 3 65 n.d. 361 2.626 3 66 281.8 (C) 361 2.68 3 67 138.0 (C) 405 1.16 4 69 n.d. 403 2.438 3 75 186.5 (C) 362 2.087 3 0" LCMS M.p. (°C) [M+H]+ Rt N0. Method 76 124.5 C 351 2.327 3 91.1 (B) 333 2.149 3 266.7 (C) 377 2.314 3 n.d. 344 1.902 3 288.4 (C) 363 2.241 3 144.2 (B) 355 2.178 3 94.5 (A) 363 2.178 3 (10°C/min) 101.2 (A) 385 2.263 3 °C/min 133.0 (A) 85 367 2.278 3 °C/mm_ 319.2 2 3 403 0.99 1 89 136.75 D 369 2.17 5 93.7 (A, temp. grad: 434 2.33 5 3 C’C/min 86 (A, temp. grad: 3 434 2.34 5 C’C/min) 262.88 (D) 462 2.85 6 n.d. 419 2.15 5 154.9 (A, temp. grad: 405 2.16 5 3 n) n.d. 405 2.26 5 182.3 (B) 397 1.97 5 . 375 2.51 5 403 2.45 5 149.7 (A1, 148 363.2 1.79 3 °C/mm_ 363 0.36 3 156 123.7 B 359 2.06 5 WO 95311 —171— 0" LCMS M.p. (°C) [M+H]+ Rt N0. Method 161 82.7 B 383 1.92 5 96.7 (B) 387 2.10 5 276.2 (B) 403 1.70 5 124.7 (B) 367 2.02 5 174.13 (D) 469 2.72 5 n.d 368 1.81 5 >300 (A) 388 2.28 1 354 2.02 1 374 2.02 5 60.7 (A, temp. grad: 382 1.97 5 3 C’C/min 192 155.9 B 402 2.43 5 402 2.31 5 402 2.26 5 195 75.9 (B) 398 2.08 5 136.9 (B) 368 2.18 5 146.6 (A, temp. grad: 392 2.37 5 3 C’C/min) 112.8 (B) 368 2.09 5 112.8 (A) 432 2.37 1 255.8 (B) 388 2.35 5 . 388 2.31 5 384 2.21 5 459 2.91 6 211 n.d 374 1.99 1 212 n.d 514 1.44 11 213 n.d 480 1.32 7 215 n.d 407 1.33 167.3 (A, 218 temp. grad: 407 2.50 5 3 C’C/min) 221 n.d 513 2.40 5 0" LCMS M.p.(°C) [M+H]+ Rt N0. Method 223 n.d. 451 2.97 2 407 2.80 2 425 1.40 7 445 1.25 12 432 1.12 432 1.11 418 0.96 . . 437 2.88 13 417 0.99 7 432 2.44 5 420. 1455 2.38 13 244 188.41 D 373.0626 --0.3rnDa 1.11 12 245 n.d. 446.1820 2.0 13 n.d. 448.1765 (--0.5mDa) 2.43 13 155.12 (D) 391.1184 mDa) 2.33 13 158.03 (D) 447.1756 (0.0mDa) 2.78 13 416.1698 151.45 (D) 2.29 13# (-0.0mDa) n.d. 437.0994 (--0.2mDa) 1.94 13 n.d. 430.1857 (--0.3rnDa) 2.63 13 n.d. 464.1469 --0.4rnDa 2.88 13 450.1310 --0.2mDa 2.52 13 430.1855 --0.1mDa 2.48 13 257 n.d. 46 --0.1mDa 2.38 13 444.2012 --0.1mDa 2.7 13 259 115.50 D 430.1856 --0.2mDa 2.49 13 442.1852 141.74 (D) 2.56 13 (-0.2mDa) n.d. 430.1202 (+0.1mDa) 2.54 13 . 464.1463 (-0.2mDa) 2.71 13 n.d. 430.1199 (-0.2mDa) 2.55 13 n.d. 65 (--0.0mDa) 2.72 13 n.d. 439.0951 (--0.2mDa) 2.50 13 173.08 430.1853 -0.lrnDa 2.51 13 -l73- LCMS Mp ( C)o [M+H] Method 13130 4442012 (+0 lmDa) 2.9 n.d. = not determined SFC-MS General grocedure The SFC measurement was performed using Analytical system from Berger instrument comprising a FCM-1200 dual pump fluid control module for ring carbon dioxide (C02) and modifier, a CTC ics tic liquid sampler, a TCM-20000 thermal control module for column heating from room temperature to 80°C. An Agilent 1100 UV photodiode array detector equipped with a high-pressure flow cell standing up to 400 bars was used. Flow from the column was split to a MS spectrometer. The MS detector was configured with an atmospheric pressure ionization source.The following ionization parameters for the Waters ZQ mass spectrophotometer are: corona: 9ua, source temp: 140°C, cone: 30 V, probe temp 450°C, tor 3 V, desolvatation gas 400L/hr, cone gas 70 L/hr. Nitrogen was used as the nebulizer gas. Data acquisition was performed with a Waters-Micromass MassLynx-Openlynx data system.
Table 4. Analytical SFC-MS Methods (Flow expressed in mL/min; column temperature (T) in CC; Pressure in Mpa).
Method Column Mobile Phase Flow T Pressure cel OD-H COz/EtOH (0.3% l 250x4.6mm, 5um 3 35 100 _ IPrNHz) 70/30 Da1cel Chiralpak IC OH (0.3% 2 250x4.6mm 5um 3 35 100 _ ) 70/30 Da1cel Ch1ralpak IC COz/EtOH (0.3% 3 250x4.6mm 5um 3 35 100 _ IPrNHZ) 60/40 Da1cel — 174 — Method Mobile Phase Pressure _ COz/MeOH (0.3% Ch1ralpak IC lPrNH2)/1PrOH. 4 6mm, 5mm _ (0.3% lPrNHz) Da1cel 80/10/10 _ COz/MeOH (0.3% Ch1ralpak AD-H lPrNH2)/1PrOH. 150X4.6mm, 5um 3 35 100 _ (0.3% ) Da1cel 60/20/20 Table 5. Analytical SFC data — Rt means retention time (in minutes), [M+H]+ means the protonated mass of the compound, method refers to the method used for SFC/MS analysis of enantiomerically pure nds. The measurement was compared against the mixture.
Co. Isomer Rt [M+H] UV Area % Method No. Elution Order 130 2.65 401 100 A 1 129 3.84 401 100 B 1 120 3.28 417 100 A 2 121 4.40 417 100 B 2 119 A 3 118 B 3 116 A 4 115 B 4 184 A 5 185 5.22 420 100 B 5 Optical Rotations Optical rotations were ed on a Perkin-Elmer 341 polarimeter with a sodium lamp and reported as follows: [0L]0 (9», c g/ 100ml, solvent, TOC). [ahT = (100(1) / (l X c) : where l is the path length in dm and c is the concentration in g/100 ml for a sample at a temperature T (C) and a wavelength 9» (in nm). If the wavelength of light used is 589 nm (the sodium D line), then the symbol D might be used instead. The sign of the rotation (+ or -) should always be given. When using this equation the tration and solvent are always provided in parentheses after the rotation. The rotation is reported using degrees and no units of concentration are given (it is assumed to be g/100 ml).
Table 6. O otical on data.
Concentration Temp.
Solvent w/v % ° C 0.59 USH1 20 UUUU SSSSmmmm 20 USn1 No UUUU SSSSmmmm 2"11 UUUUSSS "11’11’11Sn1 NNNNNNNN OOOOOOOO USS"U’fi MN 00 cooSS"11’11 NM 00 USn1 Ii0 USS"U’fi MN 00 cooSS"11’11 NM 00 USn1 Ii0 USn1 No WO 95311 Concentration w/V % 2014/061478 Concentration w/V % 589 0.50 589 0.51 W WO 95311 Concentration w/V % 2014/061478 Concentration w/V % 589 0.50 589 0.51 WO 95311 Concentration w/v % 262 589 263 589 264 589 266 589 267 20.3 589 0.51 DVIF 20 Co. No. 237: 1H NMR (500 MHz, CDC13) 8 ppm 1.72 (d, J=6.6 Hz, 3 H) 2.96 (d, J=5.2 Hz, 3 H) 4.05 (s, 3 H) 4.42 (dd, J=13.7, 7.1 Hz, 1 H) 4.53 - 4.59 (m, 1 H) 4.64 (dd, J=13.6, 4.0 Hz, 1 H) 4.70 - 4.78 (m, 1 H) 6.76 (s, 1 H) 6.84 (d, J=5.2 Hz, 1 H) 7.78 (d, J=8.7 Hz, 1 H) 7.77 (s, 1 H) 7.88 (d, J=8.4 Hz, 1 H) 8.13 (d, J=5.2 Hz, 1 H) cological examples The compounds provided in the present invention are negative allosteric modulators of mG1uR2. These compounds appear to inhibit glutamate responses by g to an a110steric site other than the glutamate binding site. The response of mG1uR2 to a concentration of glutamate is decreased when compounds of Formula (I) are present. Compounds of Formula (I) are ed to have their effect substantially at mG1uR2 by virtue of their ability to reduce the fimction of the receptor. The effects of negative a110steric modulators tested at mG1uR2 using the [35S]GTPyS binding assay method bed below and which is suitable for the identification of such compounds, and more particularly the compounds according to Formula (I), are shown in Table 7. 1) [35$]GTPyS binding assay The [35S]GTPyS binding assay is a fimctional membrane-based assay used to study G-protein coupled receptor (GPCR) fimction whereby incorporation of a non-hydrolysable form of GTP, [3SS]GTPyS (guanosine 5’-triphosphate, labelled with gamma-emitting 35S), is measured. The G-protein 0t subunit catalyzes the exchange of guanosine 5 ’-diphosphate (GDP) by guanosine triphosphate (GTP) and on activation of the GPCR by an agonist, [3SS]GTPyS, s incorporated and cannot be cleaved to continue the ge cycle (Harper (1998) Current Protocols in Pharmacology 2.6.1-10, John Wiley & Sons, Inc.). The amount of radioactive TPyS incorporation is a direct measure of the activity of the G-protein and hence the activity of the antagonist can be determined. mGlu2 receptors are shown to be preferentially coupled to God-protein, a preferential coupling for this method, and hence it is widely used to study receptor activation of mGlu2 receptors both in recombinant cell lines and in tissues. Here we describe the use of the [3SS]GTPyS binding assay using membranes from cells transfected with the human mGlu2 receptor and adapted from Schaffhauser et al. (Molecular Pharmacology, 2003, 4:798-810) for the detection of the negative allosteric modulation (NAM) ties of the compounds of this invention.
Membrane preparation CHO-cells were ed to pre-confluence and stimulated with 5 mM butyrate for 24 h. Cells were then collected by scraping in PBS and cell suspension was centrifuged (10 min at 4000 RPM in benchtop fuge). Supernatant was discarded and pellet gently resuspended in 50 mM Tris-HCl, pH 7.4 by mixing with an Ultra Turrax homogenizer. The sion was centrifuged at 12,400 RPM (Sorvall Fl4S- 6x250Y) for 10 s and the supernatant discarded. The pellet was homogenized in mM Tris-HCl, pH 7.4 using an Ultra Turrax homogenizer and centrifuged again (13,000 RPM, 20 min, 4 CC). The final pellet was resuspended in 50 mM Cl, pH 7.4 and stored at —80 CC in appropriate aliquots before use. Protein concentration was determined by the Bradford method (Bio-Rad, USA) with bovine serum albumin as [35SZ GTPzS binding assay Measurement ofmGluR2 negative allosteric modulatory activity of test compounds was performed as follows. Test compounds and glutamate were diluted in assay buffer containing 10 mM HEPES acid, 10 mM HEPES salt, pH 7.4, 100 mM NaCl, 3 mM MgClz and 10 uM GDP. Human mGlu2 receptor-containing nes were thawed on ice and diluted in assay buffer supplemented with 18 ug/ml saponin.
Membranes were pre-incubated with compound together with a predefined (~EC80) concentration of glutamate (60 uM) for 30 min at 30 °C. After addition of [3SS]GTPyS (fc. 0.1 nM), assay mixtures were shaken briefly and r incubated to allow 2014/061478 [3SS]GTPyS incorporation on activation (30 minutes, 30 CC). Final assay mixtures contained 7 ug of membrane protein in 10 mM HEPES acid, 10 mM HEPES salt, pH 7.4, 100 mM NaCl, 3 mM MgClz, lO uM GDP and 10 ug/ml saponin. Total reaction volume was 200 ul. Reactions were ated by rapid filtration through Unifilter-96 GF/B plates (Perkin Elmer, Massachusetts, USA) using a 96-well filtermate universal harvester. Filters were washed 6 times with ice-cold 10 mM NaH2PO4/10 mM 4, pH 7.4. Filters were then air-dried, and 30 ul of liquid scintillation cocktail (Microscint-O) was added to each well. Membrane-bound radioactivity was counted in a Topcount.
Data analysis The concentration-response curves of representative compounds of the present invention were generated using the Lexis software interface (developed at J&J). Data were ated as % of the control glutamate response, defined as the response that is generated upon on of an ECgo-equivalent concentration of glutamate. Sigmoid tration-response curves plotting these percentages versus the log concentration of the test compound were analyzed using non-linear regression analysis. The concentration producing half-maximal inhibition was calculated as the IC50.
The pICso values were calculated as the —log ICso, when the ICso is expressed in M.
Emax is defined as the ve maximal effect (i.e. maximal % inhibition relative to the control glutamate response).
Table 7. Pharmacological data for compounds according to the invention.
WO 95311 Co. No. Co. No. 88 7.3 102 89 7.38 104 90 8.51 103 91 7.25 103 WO 95311 — 184 — Co. No. Co. No. 92 129 94 131 95 132 96 133 97 134 98 135 99 136 100 137 101 138 102 139 103 140 108 105 106 109 143 104 107 7.75 114 144 7.02 103 108 108 145 105 109 7.73 107 146 7.78 105 110 8.29 108 147 8.24 106 111 6.53 108 148 5.25 100 112 7.45 103 149 <43 49 114 8.15 104 151 5.92 103 115 108 152 105 116 6.25 105 153 7.84 103 109 154 104 119 5.6 100 156 7.25 106 120 106 157 104 121 4.79 75 158 7.6 106 122 8.43 108 159 7.87 104 123 8.18 107 160 6.97 106 124 8.52 108 161 4.81 76 125 105 162 102 126 8.24 108 163 7.96 103 127 7.56 103 164 8.26 107 128 6.23 104 165 7.71 102 WO 95311 C0.N0. C0.N0. 166 . 203 105 107 168 106 205 102 169 8.2 105 206 7.75 111 170 107 207 109 171 4.77 94 208 7.65 107 172 5.98 105 209 8.19 104 173 8.36 106 210 7.63 105 174 8 105 211 5.43 92 175 102 176 5.2 85 213 n.t. 177 8.03 105 178 7.62 107 215 n.t. 180 106 181 6.38 103 218 n.t. 182 106 183 7.64 103 220 n.t. 184 6.56 105 221 185 8.22 104 222 186 7.42 102 223 .. 187 108 188 8.39 108 225 n.t. 189 102 190 6.68 105 227 n.t. 191 109 228 192 106 193 7.72 103 230 n.t. 194 107 195 5.39 92 232 n.t. 196 7.3 107 233 197 6.8 104 234 198 7.04 104 235 . 102 236 105 200 8.23 105 237 8.5 111 201 8.08 105 238 5.67 103 202 7.99 103 239 n.t. n.t. means not tested 2) Reversal of the effect of the mGluR2 PAM JNJ—42153605 0n scopolamine- induced ocomotion Apparatus Motor activity was measured in microprocessor-based motor activity arenas (closed gray PVC cylinders with a height of 39 cm and a diameter of 31 cm). Each arena was placed on an infrared LED (8 x 8 LEDs) lit box (white PVC squared box; 40 X 40 cm2; height 12.5 cm. An infrared-sensitive tube camera and a white light source were mounted to the ceiling above the ation chamber to track the animal. The total distance traveled (cm) was recorded and analyzed using the Noldus Ethovision XT Video Tracking System (Version 7.0.418; Noldus, Wageningen, The Netherlands).
The intensity of the light within the activity cages (measured in the centre at the level of the floor) ranged between 4 and 8 LUX.
General Procedure The rats were pretreated with test nd or vehicle at 60 min before the start of the activity recordings and placed into dual cages. The rats were challenged with 153605 (3-(cyclopropylmethyl)—7-(4-phenylpiperidinyl) (trifluoromethyl)[1,2,4]triazolo[4,3 -a]pyridine; WO2010/130424; Cid et al. J. Med.
Chem. 2012, 55, 8770-8789) (20 mg/kg, iv.) 30 min before the start ofthe activity recording combined with scopolamine (0.16 mg/kg, iv.) just before the start of the ty ements. Immediately after the injection of scopolamine, the rats were placed into the ty monitors and total distance travelled over the first 30 min was measured.
Solvent-pretreated l rats.
Frequency distributions obtained in historical series of solvent-pretreated control rats are given in figure 1 and Table 8 below. Animals receiVing the combination of JNJ-42153605 and scopolamine (n = 433) almost always travelled a distance of less than 1500 cm (< 1500 cm) (only 2.5% of the control rats travelled a distance of more than 1500 cm (> 1500 cm)). On the other hand, animals challenged with scopolamine alone (n = 215) always travelled a total distance of more than 1500 cm (> 1500 cm) and almost always (in 95.8% of the rats) a distance of more than 4400 cm (> 4400 cm).
Rats that did not receive any challenge travelled almost always a distance of more than 1500 cm (> 1500 cm) (in 93.3% of the rats) and less than 4400 cm (< 4400 cm) (in 98.9% of the rats). For reversal of the inhibitory effect of JNJ-42153605 on the scopolamine-induced hyperlocomotion, two all-or-none criteria were adopted: (1) reversal: total distance > 1500 cm; (2) normalization: total distance > 4400 cm.
The results on the reversal of the effect of 153605 are shown in table 9 below.
Table 8. Frequency distributions obtained in historical series of solvent-pretreated control rats. Ntested means number of animals tested.
Median cm Combination . .
N0 challenge 2618 93.3 1.1 638 Scopolamine 7246 100 95.8 215 Table 9. Reversal of the effect of NJ 42153605 on scopolamine-induced hyperlocomotion. ED50 means ive dose; PO means oral route; SC means subcutaneous route.
Co. No. Route ED50 SC 2 10 16 SC 2 10 PO 1.26 WO 95311 (m.Nm (m.Nm 2 201 186 147 6 142 200 236 4 127 104 14 103 19 102 3 100 99 9 95 13 180 18 182 45 237 46 242 43 251 47 255 44 256 152 257 3) V-maze test The V-maze-test is a two-trial short term Visual-spatial working memory task based on spontaneous exploration of a new and a familiar arm in a 2-arm maze (Embrechts et al. (2013) "Longitudinal characterization of the TauPS2APP mouse model of Alzheimer’s disease in a two trial discrimination task of Visuo-spatial recognition memory", 45th European Brain and Behaviour Society Meeting 6-9 September 2013, Munich, Abstract P202). Performance in this task can be disrupted by a low dose of PCP, such that the animals do not discriminate anymore between the new and a familiar arm.
Method Male Long Evans rats er, France, body weight 280 to 295 g) were group housed in enriched indiVidually ventilated cages and habituated to environmental conditions for 5 days. After acclimatization, animals were single housed for 4 days until g.
During this period animals were handled for 2 min per day and received sham dosing -l89- once a day for 3 days prior to the test. The V-maze consisted of two arms (LxWxH: 70><10><30 cm) at a 900 angle to each other to form a V-shaped maze connected by guillotine doors to a center zone. The walls of each arm were of a different context displaying horizontally black and white striped in one arm vs. uniform black walls in the other. Background red illumination was provided via the bottom of the maze and a top view video camera above the rm was used for video recording of the experiments. The animal’s exploration of each arm was automatically quantified using Ethovision XT 7.0 (Noldus, The Netherlands). Animals were d with Co. No. l or its vehicle (20% HP-B-CD + 1 eq. HCl) administered p.0. 4 h before the start of the test. PCP (0.75 mg/kg s.c.) or its vehicle (0.9% NaCl solution) was administered 30 min prior to the test. The test consisted of 2 sessions of 5 min each: in the first session (exploration) the animal was placed in the center zone and given access to one of both arms (=familiar). After 5 min, the animal was taken out of the maze, the door of the other arm (new) was also opened, and the animal was put back in the center zone for a second session (choice). The time spent in the familiar and new arm respectively during the choice session was recorded for 5 min.
Results Co. No. l was evaluated in rats in a series of dose-response studies evaluating doses from 0.16 to 10 mg/kg. While control s (treated with vehicle of the test nd and the vehicle of PCP) displayed a strong preference for ation of the new vs. the familiar arm in the second session, the PCP-treated rats did not discriminate anymore n both arms in each of these studies. PCP-challenged rats that were pretreated with Co. No. l at doses from 0.32 mg/kg onwards showed again a clear preference for the new arm (Figure 2). This reversal effect t PCP was observed up to the highest dose tested (10 . 4) Reserpine interaction test in rats Some exemplified compounds were observed to induce mydriasis in rats.
It was investigated to what extent the mydriatic action of test compounds was sufficient to counteract the miosis induced by the monoamines-depleting agent reserpine (10 mg/kg; SC) in Wiga rats. Test compounds induced mydriasis before the reserpine challenge (time = -l h unless otherwise stated; Table 10).
For ce, Co. No. 1 induced mydriasis before the reserpine challenge (ED50: 1.78 mg/kg s.c.; 1.55 mg/kg p.o., -l h; 0.89 mg/kg, p.o., -4 h) and reversed the reserpine- induced ptosis (ED50: 1.03 mg/kg s.c.; 0.78 mg/kg p.o., -l h; 0.78 mg/kg, p.o., -4 h), miosis (ED50: 4.1 mg/kg s.c.; 9.4 mg/kg p.o., -l h; 9.4 mg/kg, p.o., -4 h) and sedation (ED50: 9.4 mg/kg s.c.; 7.1 mg/kg p.o., -l h; 14 mg/kg, p.o., -4 h). The effects are illustrated in Figure 3. Co. No. 1 did not affect the tail-pinch response before reserpine nor the reserpine-induced blockade of the tail-pinch response and did not induce scratching or hyperemia after reserpine. The reference mGlu2 NAMs RO-4995819 (40 mg/kg, p.o.), RO-4491533 (40 mg/kg, p.o.; 10 mg/kg, s.c.) and [CAS 1] (40 mg/kg, s.c.) were devoid of these ctions with reserpine.
Without Wishing to be bound by theory, the observed effect may be mediated by a mechanism different from, and onal to, mGluR2 NAM activity.
Table 10. Reversal of reserpine-induced ptosis (reserpine; 10 mg/kg; SC; -lh) in Wiga rats.
C0.N0. Route 40 P0 "— 33 P0 26 P0 31 PO 2 PO 186 PO 200 P0 P0 41 P0 38 P0 36 P0 24 P0 34 P0 22 P0 79 P0 78 P0 82 P0 81 P0 80 PO 148 P0 83 PO WO 95311 - l9l - Co. No. Route 86 PO 187 PO 149 P0 84 P0 45 PO 150 P0 85 PO 190 PO 191 P0 44 PO 194 PO 195 PO 161 PO 167 PO 147 PO 171 PO 172 PO 129 PO 125 PO 119 PO 116 PO 244 PO ) R01284 interaction test in rats The relative ability of Co. No. l to increase palpebral g was also studied in rats nged with another monoamines ing agent, viz. Rol284 (1.25 mg/kg, s.c.). Effects on body temperature immediately before the injection of Rol284 were also measured. The cumulative palpebral opening score (every 5 min over a 1-h period) was used for evaluation. The median cumulative palpebral opening in solventpretreated control animals (n = 70) was 18; a scores > 25 occurred in only 1.4% of these control animals and was adopted as all-or-none criterion for drug-induced reversal of the Rol284-induced palpebral ptose. Co. No. 1 increased palpebral opening to scores > 25 (ED50: 0.51 mg/kg, p.o.) without affecting body temperature (> 10 mg/kg, p.o.). -l92- 6) al of LYinduced decrease of palpebral opening in apomorphinechallenged rats.
Male Wiga Wistar rats (Crl:Wl; Charles River Germany; 220 :: 40 g) were housed under standard laboratory conditions (21 :: 2 0C; 50-65% ve humidity; dark cycle set at 12 h; lights on at 6.00 h) and fasted overnight prior to the start of the experiments (tap water remained available ad libitum). During the test period, they were housed in individual cages. The local l Committee ed all studies in compliance with the Declaration of Helsinki. Palpebral opening was scored every 5 min over the first hour after injection of phine (1.0 mg/kg, iv) in animals either ated or not pretreated with LY-404039 (2.5 mg/kg, 5.0.) at l h prior to the apomorphine injection. The animals were also pretreated with test compound or solvent at a ned interval before phine challenge. The score system was: (5) exophthalmos, (4) wide open, (3) open for three-quarters, (2) half open, (1) open for one-quarter, (0) closed. The scores for palpebral opening were cumulated over the 60- min observation period. A cumulative palpebral opening score > 26 was selected for drug-induced reversal of the LYinduced decrease of palpebral opening (occurrence in 3.2% of control animals pretreated with LY-404039 (n = 154) versus in 99.5% of control rats not pretreated with LY-404039 (n = 6335)).
Table 1 la shows the palpebral opening score in control animals receiving apomorphine alone and in animals receiving apomorphine and LY-404039. In animals receiving apomorphine alone the median palpebral opening is 43 whereas in animals receiving apomorphine and LY-404039, the median palpebral opening is 17. In animals treated with apomorphine alone, the palpebral opening score is almost always (in 95.5% of the rats) greater than 34, whereas in s treated with the combination rphine + 039) only 3.2% of the animals show palpebral opening greater than 26.
Table 11a. Palpebral opening score in control animals.
Apomorphine alone Apomorphine + LY-404039 Measurement (11 = 6335) (n = 154) Palpebral opening score Median score: 43 17 Occurrence score > 26 (%): 99.5 3.2 Occurrence score > 34 (%): 95.9 0.0 -l93- Table 11b. Reversal of LYinduced decrease of palpebral opening in phine challenged rats.
Co. No. Route ED50 33 PO >25 31 PO 210 1 PO 0.45 SC 0.3 8 PO 5 PO 11.22 2 PO 0.50 PO >10 45 PO 0.79 46 PO 0.32 44 PO 0.50 167 PO >40 147 PO 1.26 172 SC >40 140 PO 1.99 7) Reversal of mGluRZ-agonism in hippocampal brain slices Introduction Electrophysiology recordings of field tory postsynaptic potentials (fEPSPs) in acute hippocampal brain slices represent a model for testing synaptic transmission and plasticity. The effect of Co. No. l on ic transmission and plasticity in dentate gyrus synapses was investigated using this model. This region was chosen because of the high expression of mGluR 2 (Shigemoto et al., The Journal ofNeuroscience, r 1, 1997, 17(19), 7503-7522).
Methods Recordings of fEPSPs were made from hippocampal brain slices using a multi- electrode array (MEA) biochip, and 3-dimensional- (3D) tip odes, according to a standard ol. These recordings were used to monitor glutamate-mediated synaptic transmission (Figure 4).
Results Superfusion of rat hippocampal brain slices with the mGlu2/3-specific agonist LY-354740 (1 uM) depressed fEPSP by 50% within 15 min of application (Figure 5) and was associated with an increase of the paired-pulse ratio (PPR), indicating a —194— presynaptic mechanism. Fifteen min after the application of 10 uM Co. No. 1 the depression of fEPSP had recovered by 80%. This was associated with a decrease of the PPR, indicating an increase in neurotransmitter release (Figure 5, n = 17 slices from 4 rats).
Subsequently, the effects of Co. No. 1 on ic function using long-term iation (LTP) protocols in the dentate gyrus (Goeldner et. al., Neuropharmacology 2013, 64, 337-346) were evaluated.
Small ude LTP (110%) was induced using isolated glutamatergic-mediated fEPSP: trains of theta-burst ation that are known to induce LTP at these particular synapses were d (Dinklo et al., J. Pharmacol. Exp. Ther. 2011, 336(2), 560-574). In the ce of 10 uM Co. No. 1, the magnitude of LTP was enhanced by 150% compared to baseline (p=0.005). Also noteworthy is the finding that the post-theta potentiation (PTP) in the presence of 10 uM Co. No. 1 was significantly different from vehicle treatment: 160% vs. 120% respectively (p=0.01) (Figure 6, 22 slices from 4 SD rats). At the end of the experiments, addition of 1 mM kynurenic acid to block glutamatergic ransmission, confirmed that the ynaptic se is mediated by glutamate neurotransmission.
Discussion LY-354740 stimulates presynaptic mGlu2/3 receptors to limit the release of glutamate.
Furthermore, the effects of Group II mGluR agonists and antagonists in rodent models of cognition are totally absent in mGluR2 knock-out mice (Higgins et al.
Neuropharmacology, 2004, 46, 907-917). Co. No. 1 reversed synaptic depression evoked by the mGlu2/3 -agonist LY-354740. These data illustrate that Co. No. 1 is able to restore depressed synaptic ission in rat hippocampal slices in vitro. The increase in network excitability, as a result of enhanced excitatory neurotransmission, affected the threshold of LTP induction. Thus, LTP was efficiently induced by weak theta stimulation, but only when Co. No. 1 was pre-applied. Thus, the compound might act as a cognitive enhancer via an ability to e the synaptic strength in glutamatergic synapses and by priming the system for enhanced LTP.
Prophetic composition examples e ingredient" as used throughout these examples relates to a final compound of Formula (I), the pharmaceutically acceptable salts thereof, the solvates and the stereochemically isomeric forms and the tautomers thereof.
Typical es of recipes for the formulation of the invention are as follows: 2014/061478 1. Tablets Active ingredient 5 to 50 mg cium phosphate 20 mg Lactose 30 mg Talcum 10 mg Magnesium stearate 5 mg Potato starch ad 200 mg In this Example, active ingredient can be replaced with the same amount of any of the compounds according to the present invention, in particular by the same amount of any of the exemplified compounds. 2. Suspension An aqueous suspension is prepared for oral administration so that each 1 milliliter contains 1 to 5 mg of one of the active nds, 50 mg of sodium carboxymethyl cellulose, 1 mg of sodium benzoate, 500 mg of sorbitol and water ad 1 ml. 3. Injectable A parenteral composition is prepared by stirring 1.5 % by weight of active ingredient of the invention in 10% by volume propylene glycol in water. 4. Ointment Active ient 5 to 1000 mg Stearyl alcohol 3 g ne 5 g White petroleum 15 g Water ad 100 g In this Example, active ingredient can be replaced with the same amount of any of the compounds according to the present invention, in particular by the same amount of any of the exemplified compounds.
Reasonable variations are not to be ed as a departure from the scope of the invention. It will be obvious that the thus described invention may be varied in many ways by those skilled in the art.
WO 95311 -l96-

Claims (29)

1. A compound of Formula (I) 0 R2 R\NM R3 R4 (1) or a stereoisomeric form thereof, wherein R1 is phenyl or 2-pyridinyl, each optionally substituted with one or more substituents each independently selected from the group of halo, C1_4alkyl, mono- or 10 poly-haloC1_4alkyl, -O-C1_4alkyl, -C1_4alkyl-O-C1_4alkyl, mono- or poly-haloC1_4alkyloxy, -C1_4alkyl-OH, C1_4alkylthio, mono- or poly-haloC1_4alkylthio, cyano, C3_7cycloalkyl optionally substituted with trifluoromethyl, and —SF5; or is 15 R2 is ed from R5 N\ R6 R5 U \ N i and : wherein R5 and R6 are each independently selected from the group of hydrogen, halo, cyano, C1_4alkyl, lkyl-OH, cloalkyl, mono- or poly-haloC1_4alkyl, -C1_4alkyl-O-C1_4alkyl, -O-C1_4alkyl, mono- or poly-haloC1_4alkyloxy, 20 l-acetylazetidinyl, and NR’R”; wherein R’ is selected from hydrogen and C1_4alkyl; R” is selected from hydrogen and C1_4alkyl; or R’ and R” together with the Nitrogen atom to which they are attached form a heterocyclic group selected from the group of l-azetidinyl, l-pyrrolidinyl, 25 l-piperidinyl, razinyl, and 4-morpholinyl; wherein each of the heterocyclic groups may be optionally substituted with a tuent selected from halo, hydroxyl, C1_4alkyl, mono- or poly-haloC1_4alkyl, and —(CO)C1_4alkyl; R3 is selected from hydrogen and C1_4alkyl; -l97- R4 is selected from the group of hydrogen, C1_4alkyl, mono- or poly-haloC1_4alkyl, -C1_4alkyl-O-C1_4alkyl, and -C1_4alkyl-OH; or a N—oxide, or a pharmaceutically acceptable salt or a solvate thereof.
2. A compound according to claim 1, or a stereoisomeric form thereof, wherein R1 is phenyl or 2-pyridinyl, each ally substituted with one or more substituents each independently selected from the group of halo, C1_4alkyl, mono- or poly-haloC1_4alkyl, -O-C1_4alkyl, -C1_4alkyl-O-C1_4alkyl, mono- or poly-haloC1_4alkyloxy, -C1_4alkyl-OH, mono- or poly-haloC1_4alkylthio, cyano, and 10 —SF5;oris __I_CEO] R2 is selected from R6 R5 i and : 15 wherein R5 and R6 are each independently selected from the group of hydrogen, halo, cyano, C1_4alkyl, -C1_4alkyl-OH, C3_7cycloalkyl, mono- or poly-haloC1_4alkyl, -C1_4alkyl-O-C1_4alkyl, -O-C1_4alkyl, mono- or poly-haloC1_4alkyloxy, and NR’R”; wherein R’ is selected from hydrogen and C1_4alkyl; R” is selected from hydrogen and C1_4alkyl; or 20 R’ and R” together with the Nitrogen atom to which they are attached form a heterocyclic group selected from the group of l-azetidinyl, l-pyrrolidinyl, and l-piperidinyl; n each of the heterocyclic groups may be optionally substituted with a halo substituent; R3 is selected from hydrogen and C1_4alkyl; 25 R4 is ed from the group of en, C1_4alkyl, mono- or poly-haloC1_4alkyl, -C1_4alkyl-O-C1_4alkyl, and -C1_4alkyl-OH; or a N—oxide, or a pharmaceutically acceptable salt or a solvate f.
3. A compound according to claim 1 or 2, or a isomeric form thereof, wherein 30 R1 is phenyl, optionally substituted with one or more tuents each independently selected from the group of halo, C1_4alkyl, mono- or aloC1_4alkyl, -O-C1_4alkyl, mono- or poly-haloC1_4alkyloxy, cyano and —SF5; or is -l98- "CE? R2 is selected from R6 R5 i and : wherein R5 and R6 are each independently selected from the group of hydrogen, C1_4alkyl, mono- or poly-haloC1_4alkyl, -C1_4alkyl-O-C1_4alkyl, -O-C1_4alkyl, and NR’R”; wherein R’ is selected from hydrogen and C1_4alkyl; R” is selected from en and kyl; 10 R3 is selected from hydrogen and C1_4alkyl; R4 is selected from the group of hydrogen, C1_4alkyl, mono- or poly-haloC1_4alkyl, -C1_4alkyl-O-C1_4alkyl, and -C1_4alkyl-OH; or a ceutically acceptable salt or a e thereof. 15
4. The compound according to any one of claims 1 to 3, or a stereoisonieric form thereof, wherein R1 is phenyl, optionally substituted with one or more substituents each independently selected from the group of halo, C1_4alkyl, mono- or poly-haloC1_4alkyl, -O-C1_4alkyl, mono- or poly-haloC1_4alkyloxy, cyano and —SF5; or is CEO/ 20 O R2 is selected from R5 N\ R6 R5 U \ N i and : wherein R5 and R6 are each independently selected from the group of hydrogen, 25 kyl, -C1_4alkyl-O-C1_4alkyl, -O-C1_4alkyl, and NR’R”; wherein R’ is hydrogen; R” is hydrogen; R3 is selected from en and C1_4alkyl; R4 is selected from the group of hydrogen and C1-4alkyl; or a pharmaceutically acceptable salt or a solvate f.
5. The compound according to any one of claims 1 to 4, or a isomeric form 5 thereof, wherein R1 is phenyl, optionally substituted with one or more substituents each independently selected from the group of halo, C1-4alkyl, poly-haloC1-4alkyl and –SF5; R2 is selected from R5 N R6 R5 10 and wherein R5 and R6 are each independently selected from the group of hydrogen, C1-4alkyl and 4alkyl; R3 is selected from hydrogen and C1-4alkyl; R4 is hydrogen; 15 or a pharmaceutically acceptable salt or a solvate thereof.
6. A compound according to any one of claims 1 to 4, or a stereoisomeric form thereof, wherein R1 is selected from the group of F Cl F3C F3C ; ; F3C F3C ; ; Cl CF3 Cl Cl Cl ; ; and ; and the rest of variables are as d in any one of claims 1 to 4.
7. A compound according to claim 1 or 2, wherein the compound is F N F O or a N-oxide, or a pharmaceutically acceptable salt or a solvate thereof.
8. The compound according to claim 7 wherein the compound is the free base, the 5 hydrochloride salt, the sulfate salt, the methane sulfonate salt or the e salt.
9. The compound according to claim 7, wherein the compound is or a pharmaceutically acceptable salt or a solvate thereof.
10. A compound according to claim 1 or 2, wherein the compound is F N F O or a pharmaceutically acceptable salt or a solvate thereof. 15
11. A pharmaceutical ition comprising a eutically effective amount of a compound according to any one of claims 1 to 10 and a ceutically acceptable carrier or excipient.
12. A compound according to any one of claims 1 to 10 or a pharmaceutical 20 composition according to claim 11 for use as a ment.
13. A compound according to any one of claims 1 to 10 or a pharmaceutical composition according to claim 11 for use in the treatment or in the prevention of central s system conditions or a diseases selected from mood disorders; delirium, dementia, amnestic and other cognitive disorders; disorders usually first diagnosed in infancy, childhood or adolescence; substance-related disorders; schizophrenia and other psychotic disorders; somatoform ers; and omnic sleep disorder.
14. A compound according to any one of claims 1 to 10 or a ceutical composition according to claim 11 for use in the treatment or prevention of central nervous system disorders or conditions selected from depressive disorders; neurocognitive ers; evelopmental disorders; substance-related and 10 addictive disorders; schizophrenia spectrum and other psychotic ers; somatic symptom and related disorders; and omnolence disorder.
15. The compound or the pharmaceutical composition for use according to claim 13 or 14, wherein the central nervous system conditions or diseases are selected from 15 dementia or neurocognitive disorder, major depressive disorder, sion, treatment resistant depression, attention-deficit/hyperactivity disorder and schizophrenia.
16. The compound according to any one of claims 7 to 10 for use in the treatm ent or tion of major depressive er, depression, or treatment resistant depression.
17. A process for preparing the pharmaceutical composition according to claim 11, wherein a pharmaceutically acceptable carrier or excipient is intimately mixed with a therapeutically ive amount of a compound according to any one of claims 1 to 10. 25
18. Use of a compound according to any one of claims 1 to 10 or a pharmaceutical composition according to claim 11 in the manufacture of a medicament for treating or preventing central nervous system conditions or a e selected from mood disorders; delirium, dementia, amnestic and other cognitive disorders; disorders usually first diagnosed in infancy, childhood or adolescence; substance-related disorders; 30 schizophrenia and other psychotic disorders; somatoform disorders; and hypersomnic sleep disorder.
19. Use of a compound according to any one of claims 1 to 10 or a pharmaceutical composition according to claim 11 in the manufacture of a medicament for treating or 35 ting central nervous system disorders or conditions selected from depressive disorders; neurocognitive disorders; neurodevelopmental disorders; substance-related and addictive ers; schizophrenia spectrum and other psychotic disorders; somatic symptom and d disorders; and hypersomnolence disorder.
20. The use according to claim 18 or 19, wherein the central nervous system conditions or diseases are selected from dementia or neurocognitive disorder, major depressive disorder, depression, treatment resistant depression, attention-deficit/hyperactivity er and schizophrenia.
21. Use of the compound according to any one of claims 7 to 10 in the manufa cture of a medicament for treating or preventing major depressive disorder, depression, or treatment resistant depression. 10
22. A product comprising a compound according to any one of claims 1 to 10 and an additional ceutical agent, as a combined preparation for simultaneous, separate or tial use in the treatment or prevention of central nervous system ions or diseases selected from mood disorders; delirium, dementia, amnestic and other cognitive disorders; disorders usually first diagnosed in infancy, childhood or 15 adolescence; substance-related disorders; schizophrenia and other psychotic disorders; form disorders; and hypersomnic sleep disorder.
23. A product comprising a compound according to any one of claims 1 to 10 and an additional ceutical agent, as a combined preparation for aneous, separate 20 or sequential use in the treatment or tion of central nervous system conditions or diseases selected from depressive disorders; neurocognitive disorders; neurodevelopmental disorders; substance-related and addictive disorders; schizophrenia spectrum and other psychotic disorders; somatic symptom and related disorders; and omnolence disorder.
24. A compound of Formula (V) wherein R2a is halo, and R3 and R4 are as defined in any one of claims 1 to 10. 30
25. A compound ing to claim 24, having the Formula (V’) (V’).
26. A compound according to claim 24 or 25, having the Formula (I-13) or (I-13a) O I (I-13) (I-13a), or a salt thereof.
27. A compound of Formula (II) O R2 5 R3 R4 (II) wherein R2, R3 and R4 are as defined in any one of claims 1 to 10.
28. A process for the preparation of a compound according to Formula (I) as d in any one of claims 1 to 10, sing steps a) and b) 10 a) reacting a nd of Formula (V), wherein R2a is halo, with a suitable boron species, in the presence of a palladium catalyst and a suitable base and solvent, to form a compound of Formula (II) b) reacting the compound of a (II) obtained in step a) with a compound of 15 Formula (III) where X is halo, in the presence of a suitable coupling agent or a catalyst and ligand, in the presence of a base in a suitable solvent O R2 O R2 HN R1X R1 N N N (III) N R3 R4 R3 R4 (II) (I) .
29. The compound according to claim 1, substantially as herein described with 20 reference to any one of the Examples and/or
NZ713458A 2013-06-04 2014-06-03 6,7-DIHYDROPYRAZOLO[1,5-a]PYRAZIN-4(5H)-ONE COMPOUNDS AND THEIR USE AS NEGATIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS NZ713458B2 (en)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
EP13170447.0 2013-06-04
EP13170447 2013-06-04
EP13173939.3 2013-06-27
EP13173939 2013-06-27
EP14166450 2014-04-29
EP14166450.8 2014-04-29
PCT/EP2014/061478 WO2014195311A1 (en) 2013-06-04 2014-06-03 6,7-DIHYDROPYRAZOLO[1,5-a]PYRAZIN-4(5H)-ONE COMPOUNDS AND THEIR USE AS NEGATIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS

Publications (2)

Publication Number Publication Date
NZ713458A NZ713458A (en) 2021-06-25
NZ713458B2 true NZ713458B2 (en) 2021-09-28

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