US2018290966A1PendingUtilityA1
Phenyl derivatives as cannabinoid receptor 2 agonists
Est. expiryDec 9, 2035(~9.3 yrs left)· nominal 20-yr term from priority
Inventors:Olivier GavelleUwe GretherMatthias NettekovenStephan RoeverMark Rogers-EvansDidier Rombach
A61P 35/00A61P 37/06A61P 9/00A61P 3/10A61P 43/00A61P 9/10A61P 25/04A61P 29/00A61P 27/02A61P 27/00A61P 19/00A61P 1/16A61P 1/02A61P 17/02A61P 13/12A61P 1/04A61P 25/00C07D 231/12C07D 271/06C07B 2200/07C07D 413/06C07D 413/10C07C 237/22C07D 277/28C07D 331/04C07D 209/54C07D 401/10C07D 403/10C07D 305/08C07C 2601/02C07D 207/10C07D 213/61C07D 413/12C07D 205/04C07D 207/16C07C 235/52C07C 231/02A61K 31/426C07D 277/30C07D 277/22C07C 235/48C07D 207/14C07D 305/06C07C 235/46C07D 401/12C07D 403/12C07C 67/31C07C 51/09C07C 231/14A61P 27/06A61P 1/00A61P 11/00A61P 9/04A61P 19/08
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Claims
Abstract
wherein R1 to R3 are defined as in the description and in the claims. The compound of formula (I) can be used as a medicament.
Claims
exact text as granted — not AI-modified1 . A compound of formula
wherein
R 1 is cyclopropyl, alkyl or haloazetidinyl;
R 2 is cyclopropylmethoxy, alkoxy, haloalkoxy, halopyridinyl, alkylpyrazolyl or halopyrrolidinyl;
provided that at least one of R 1 and R 2 is cyclopropyl or cyclopropylmethoxy;
R 3 is —C(O)—NH—C(R 4 R 5 )—R 6 , —C(O)—R 7 or R 1 ;
R 4 and R 5 are independently selected from hydrogen, alkyl, cycloalkyl, cycloalkylalkyl, alkylsulfonylalkyl and alkyloxetanyl;
or R 4 and R 5 together with the carbon atom to which they are attached form oxetanyl or dioxothiethanyl;
R 6 is aminocarbonyl, 5-methyl-1,2,4-oxadiazol-3-yl, hydroxyalkyl, thiazolyl, alkoxycarbonyl, carboxy, difluoroazetidinylcarbonyl, 5-amino-1,2,4-oxadiazol-3-yl, alkylaminocarbonyl or aminocarbonylalkyl;
R 7 is (aminocarbonyl)(difluoro)pyrrolidinyl or (aminocarbonyl)azaspiro[2.4]heptyl; and
R 8 is 3-alkyl-1,2,4-oxadiazol-5-yl or 5-alkyl-1,2,4-oxadiazol-3-yl;
or a pharmaceutically acceptable salt or ester thereof.
2 . The compound according to claim 1 , wherein R 1 is cyclopropyl.
3 . The compound according to claim 1 , wherein R 2 is cyclopropylmethoxy, alkoxy, haloalkoxy or halopyrrolidinyl.
4 . The compound according to claim 1 , wherein R 2 is cyclopropylmethoxy, propyloxy, fluoroethoxy, trifluoroethoxy or difluoropyrrolidinyl.
5 . The compound according to claim 1 , wherein R 4 and R 5 are independently selected from the group consisting of hydrogen, alkyl, cycloalkyl and cycloalkylalkyl.
6 . The compound according to claim 1 , wherein R 4 and R 5 are independently selected from the group consisting of hydrogen, methyl, butyl, cyclopropyl and cyclopropylmethyl.
7 . The compound according to claim 1 , wherein R 6 is aminocarbonyl, 5-methyl-1-1,2,4-oxadiazol-3-yl, hydroxyalkyl or alkylaminocarbonyl.
8 . The compound according to claim 1 , wherein R 6 is aminocarbonyl, 5-methyl-1,2,4-oxadiazol-3-yl, hydroxymethyl or methylaminocarbonyl.
9 . The compound according to claim 1 , wherein R 7 is (aminocarbonyl)(difluoro)pyrrolidinyl.
10 . The compound according to claim 1 , wherein R 8 is 3-tert.butyl-1,2,4-oxadiazol-5-yl, 5-tert.butyl-1,2,4-oxadiazol-3-yl or 5-methyl-1,2,4-oxadiazol-3-yl.
11 . The compound according to claim 1 , wherein the compound is selected from the group consisting of:
(R)—N-(1-amino-4-methyl-1-oxopentan-2-yl)-3-(cyclopropylmethoxy)-4-methylbenzamide; 3-(cyclopropylmethoxy)-4-methyl-N-[2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]benzamide; 4-cyclopropyl-3-(cyclopropylmethoxy)-N-[2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]benzamide; N2-[4-cyclopropyl-3-(cyclopropylmethoxy)benzoyl]-L-leucinamide; 4-cyclopropyl-3-(cyclopropylmethoxy)-N-(1-hydroxy-2-methylpropan-2-yl)benzamide; 4-cyclopropyl-3-(cyclopropylmethoxy)-N-[2-(1,3-thiazol-2-yl)propan-2-yl]benzamide; ethyl 2-[4-cyclopropyl-3-(cyclopropylmethoxy)benzamido]-2-ethylbutanoate; 2-[4-cyclopropyl-3-(cyclopropylmethoxy)benzamido]-2-ethylbutanoic acid; 4-cyclopropyl-3-(cyclopropylmethoxy)-N-[3-(3,3-difluoroazetidine-1-carbonyl)pentan-3-yl]benzamide; 3-(cyclopropylmethoxy)-4-(3,3-difluoroazetidin-1-yl)-N-[2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]benzamide; N-[2-(5-amino-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-(cyclopropylmethoxy)-4-(3,3-difluoroazetidin-1-yl)benzamide; N2-[3-(cyclopropylmethoxy)-4-(3,3-difluoroazetidin-1-yl)benzoyl]-N-methyl-L-leucinamide; 3-(cyclopropylmethoxy)-4-(3,3-difluoroazetidin-1-yl)-N-[(2S)-1-hydroxy-4-methylpentan-2-yl]benzamide; 3-tert-butyl-5-[4-cyclopropyl-3-(cyclopropylmethoxy)phenyl]-1,2,4-oxadiazole; N-[3-(2-amino-2-oxoethyl)oxetan-3-yl]-4-cyclopropyl-3-(cyclopropylmethoxy)benzamide; N-[3-(2-amino-2-oxoethyl)-1,1-dioxothietan-3-yl]-4-cyclopropyl-3-(cyclopropylmethoxy)benzamide; 1-[4-cyclopropyl-3-(cyclopropylmethoxy)benzoyl]-4,4-difluoro-L-prolinamide; N-(3-carbamoylpentan-3-yl)-4-cyclopropyl-3-(cyclopropylmethoxy)benzamide; N2-[4-cyclopropyl-3-(cyclopropylmethoxy)benzoyl]-N-methyl-L-leucinamide; 4-cyclopropyl-3-(cyclopropylmethoxy)-N-[(2S)-1-(methanesulfonyl)-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]benzamide; 4-cyclopropyl-3-(cyclopropylmethoxy)-N-[(2R)-1-(methanesulfonyl)-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]benzamide; 5-[4-cyclopropyl-3-(cyclopropylmethoxy)benzoyl]-5-azaspiro[2.4]heptane-6-carb oxamide; 5-tert-butyl-3-[4-cyclopropyl-3-(2,2,2-trifluoroethoxy)phenyl]-1,2,4-oxadiazole; 5-tert-butyl-3-[4-cyclopropyl-3-(2,2-difluoroethoxy)phenyl]-1,2,4-oxadiazole; 4-cyclopropyl-N-[(2R)-1-cyclopropyl-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-(2,2,2-trifluoroethoxy)benzamide; 4-cyclopropyl-N-[(2S)-1-cyclopropyl-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-(2,2,2-trifluoroethoxy)benzamide; N-[3-(2-amino-2-oxoethyl)-1,1-dioxo-thietan-3-yl]-4-cyclopropyl-3-(2,2,2-trifluoroethoxy)benzamide; 4-cyclopropyl-N-[(2R)-1-(methanesulfonyl)-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-(2,2,2-trifluoroethoxy)benzamide; 4-cyclopropyl-N-[(2S)-1-(methanesulfonyl)-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-(2,2,2-trifluoroethoxy)benzamide; 5-tert-butyl-3-[4-cyclopropyl-3-(2-fluoroethoxy)phenyl]-1,2,4-oxadiazole; 4-cyclopropyl-N-[(2R)-1-cyclopropyl-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-(2,2-difluoroethoxy)benzamide; 4-cyclopropyl-N-[(2S)-1-cyclopropyl-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-(2,2-difluoroethoxy)benzamide; 4-cyclopropyl-N-[(2R)-1-cyclopropyl-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-(2-fluoroethoxy)benzamide; 4-cyclopropyl-N-[(2S)-1-cyclopropyl-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-(2-fluoroethoxy)benzamide; N-[(2S)-4-amino-2-cyclopropyl-4-oxobutan-2-yl]-4-cyclopropyl-3-(2,2,2-trifluoroethoxy)benzamide; N-[(2R)-4-amino-2-cyclopropyl-4-oxobutan-2-yl]-4-cyclopropyl-3-(2,2,2-trifluoroethoxy)benzamide; 4-cyclopropyl-N-[(2S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl]-3-[(propan-2-yl)oxy]benzamide; 4-cyclopropyl-N-[(2S)-1-cyclopropyl-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-[(propan-2-yl)oxy]benzamide; 4-cyclopropyl-N-[(2S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl]-3-(2-fluoroethoxy)benzamide; 1-[4-cyclopropyl-3-(2-fluoroethoxy)benzoyl]-4,4-difluoro-L-prolinamide; 4-cyclopropyl-N-[(2S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl]-3-(2,2,2-trifluoroethoxy)benzamide; 1-[4-cyclopropyl-3-(2,2,2-trifluoroethoxy)benzoyl]-4,4-difluoro-L-prolinamide; N-[(2S)-4-amino-2-cyclopropyl-4-oxobutan-2-yl]-4-cyclopropyl-3-[(propan-2-yl)oxy]benzamide; N-[(2R)-4-amino-2-cyclopropyl-4-oxobutan-2-yl]-4-cyclopropyl-3-[(propan-2-yl)oxy]benzamide; N-[(2R)-4-amino-2-cyclopropyl-4-oxobutan-2-yl]-4-cyclopropyl-3-(2-fluoroethoxy)benzamide; 3-tert-butyl-5-{4-cyclopropyl-3-[(propan-2-yl)oxy]phenyl}-1,2,4-oxadiazole; 3-tert-butyl-5-[4-cyclopropyl-3-(3,3-difluoropyrrolidin-1-yl)phenyl]-1,2,4-oxadiazole; 1-{4-cyclopropyl-3-[(propan-2-yl)oxy]benzoyl}-4,4-difluoro-L-prolinamide; 4-cyclopropyl-N-[(2R)-1-cyclopropyl-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-[(propan-2-yl)oxy]benzamide; 4-cyclopropyl-N-[(2R)-1-cyclopropyl-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-(6-fluoropyridin-3-yl)benzamide; N-[(2S)-4-amino-2-cyclopropyl-4-oxobutan-2-yl]-4-cyclopropyl-3-(2,2,2-trifluoroethoxy)benzamide; N-[(2R)-4-amino-2-cyclopropyl-4-oxobutan-2-yl]-4-cyclopropyl-3-(6-fluoropyridin-3-yl)benzamide; N-[(2S)-4-amino-2-cyclopropyl-4-oxobutan-2-yl]-4-cyclopropyl-3-(6-fluoropyridin-3-yl)benzamide; N-[(2S)-4-amino-2-cyclopropyl-4-oxobutan-2-yl]-4-cyclopropyl-3-(2-fluoroethoxy)benzamide; 1-[4-cyclopropyl-3-(1-methyl-1H-pyrazol-5-yl)benzoyl]-4,4-difluoro-L-prolinamide; 4-cyclopropyl-N-[(2S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl]-3-(1-methyl-1H-pyrazol-5-yl)benzamide; 1-[4-cyclopropyl-3-(6-fluoropyridin-3-yl)benzoyl]-4,4-difluoro-L-prolinamide; 4-cyclopropyl-N-[(2S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl]-3-(6-fluoropyridin-3-yl)benzamide; 4-cyclopropyl-N-[(2S)-1-cyclopropyl-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-(1-methyl-1H-pyrazol-5-yl)benzamide; 4-cyclopropyl-N-[(2S)-1-cyclopropyl-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-(6-fluoropyridin-3-yl)benzamide; N-[(2R)-4-amino-2-cyclopropyl-4-oxobutan-2-yl]-4-cyclopropyl-3-(3,3-difluoropyrrolidin-1-yl)benzamide; N-[(2S)-4-amino-2-cyclopropyl-4-oxobutan-2-yl]-4-cyclopropyl-3-(3,3-difluoropyrrolidin-1-yl)benzamide; 4-cyclopropyl-N-[(2R)-1-cyclopropyl-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-(3,3-difluoropyrrolidin-1-yl)benzamide; 4-cyclopropyl-N-[(2S)-1-cyclopropyl-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-(3,3-difluoropyrrolidin-1-yl)benzamide; 1-[4-cyclopropyl-3-(3,3-difluoropyrrolidin-1-yl)benzoyl]-4,4-difluoro-L-prolinamide; 4-cyclopropyl-3-(3,3-difluoropyrrolidin-1-yl)-N-[(2S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl]benzamide; 4-cyclopropyl-N-[(5-methyl-1,2,4-oxadiazol-3-yl)(3-methyloxetan-3-yl)methyl]-3-(2,2,2-trifluoroethoxy)benzamide; 4-cyclopropyl-N-[(5-methyl-1,2,4-oxadiazol-3-yl)(3-methyloxetan-3-yl)methyl]-3-[(propan-2-yl)oxy]benzamide; N-[3-amino-1-(3-methyloxetan-3-yl)-3-oxopropyl]-4-cyclopropyl-3-(2,2,2-trifluoroethoxy)benzamide; and 4-cyclopropyl-3-(2-fluoroethoxy)-N-[(5-methyl-1,2,4-oxadiazol-3-yl)(3-methyloxetan-3-yl)methyl]benzamide; or a pharmaceutically acceptable salt thereof.
12 . The compound according to claim 1 , wherein the compound is selected from the group consisting of:
N2-[4-cyclopropyl-3-(cyclopropylmethoxy)benzoyl]-L-leucinamide; 4-cyclopropyl-3-(cyclopropylmethoxy)-N-(1-hydroxy-2-methylpropan-2-yl)benzamide; 3-tert-butyl-5-[4-cyclopropyl-3-(cyclopropylmethoxy)phenyl]-1,2,4-oxadiazole; N-[3-(2-amino-2-oxoethyl)oxetan-3-yl]-4-cyclopropyl-3-(cyclopropylmethoxy)benzamide; N-[3-(2-amino-2-oxoethyl)-1,1-dioxothietan-3-yl]-4-cyclopropyl-3-(cyclopropylmethoxy)benzamide; 1-[4-cyclopropyl-3-(cyclopropylmethoxy)benzoyl]-4,4-difluoro-L-prolinamide; 5-tert-butyl-3-[4-cyclopropyl-3-(2-fluoroethoxy)phenyl]-1,2,4-oxadiazole; N-[(2S)-4-amino-2-cyclopropyl-4-oxobutan-2-yl]-4-cyclopropyl-3-(2,2,2-trifluoroethoxy)benzamide; 4-cyclopropyl-N-[(2S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl]-3-[(propan-2-yl)oxy]benzamide; 4-cyclopropyl-N-[(2S)-1-cyclopropyl-2-(5-methyl-1,2,4-oxadiazol-3-yl)propan-2-yl]-3-[(propan-2-yl)oxy]benzamide; and N-[(2R)-4-amino-2-cyclopropyl-4-oxobutan-2-yl]-4-cyclopropyl-3-[(propan-2-yl)oxy]benzamide; or a pharmaceutically acceptable salt thereof.
13 . A process for the preparation of a compound according to claim 1 , comprising one of the following steps:
(a) reacting a compound of formula (A)
in the presence of H 2 N—C(R 4 R 5 )—R 6 , a coupling agent and a base, wherein R 2 is cyclopropylmethoxy, alkoxy or haloalkoxy;
(b) reacting a compound of formula (A) as defined above in the presence of H—R 7 , a coupling agent and a base, wherein R 2 is cyclopropylmethoxy, alkoxy or haloalkoxy;
(c) reacting a compound of formula (A) as defined above in the presence of a compound of formula (B)
and carbonydiimidazole, wherein R 8′ is methyl or tert-butyl; or
(d) reacting a compound of formula (C)
in the presence of R 2′ —X, wherein R 2′ is cyclopropylmethyl, alkyl or haloalkyl, R 8′ is methyl or tert-butyl and X is a leaving group.
14 . A compound according to claim 1 , when manufactured according to a process of claim 13 .
15 . (canceled)
16 . A pharmaceutical composition comprising a compound in accordance with claim 1 , or a pharmaceutically acceptable salt or ester thereof, and a therapeutically inert carrier.
17 .- 19 . (canceled)
20 . A method for the treatment or prophylaxis of pain, atherosclerosis, age-related macular degeneration, diabetic retinopathy, glaucoma, diabetes mellitus, inflammation, inflammatory bowel disease, ischemia-reperfusion injury, acute liver failure, liver fibrosis, lung fibrosis, kidney fibrosis, systemic fibrosis, acute allograft rejection, chronic allograft nephropathy, diabetic nephropathy, glomerulonephropathy, cardiomyopathy, heart failure, myocardial ischemia, myocardial infarction, systemic sclerosis, thermal injury, burning, hypertrophic scars, keloids, gingivitis pyrexia, liver cirrhosis or tumors, regulation of bone mass, neurodegeneration, stroke, transient ischemic attack or uveitis, which method comprises administering to a patient in need thereof an effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt or ester thereof.
21 . (canceled)Join the waitlist — get patent alerts
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