Compounds which modulate the CB2 receptor
Compounds of formula (I) are disclosed. Compounds according to the invention bind to and are agonists, antagonists or inverse agonists of the CB2 receptor, and are useful for treating inflammation. Those compounds which are agonists are additionally useful for treating pain.
1. A compound of the formula
wherein:
R 1 is phenyl optionally independently substituted with 1 to 3 substituents chosen from C 1 -C 6 alkyl (which is optionally substituted with 1 to 3 halogen atoms), C 1 -C 6 cycloalkyl, C 1 -C 6 alkoxy (which is optionally substituted with 1 to 3 halogen atoms), C 1 -C 6 alkylthio, C 1 -C 6 alkylsulfonyl, C 1 -C 6 alkoxycarbonyl, C 1 -C 6 alkylamino, C 3 -C 6 cycloalkylamino, C 1 -C 6 dialkylamino, C 1 -C 6 alkylaminocarbonyl, acylamino, C 1 -C 6 dialkylaminocarbonyl, hydroxyl, halogen, cyano, nitro, oxo, heterocyclyl, aryl and heteroaryl;
R 2 and R 3 are independently hydrogen or C 1 -C 6 alkyl; or R 2 and R 3 together with the carbon which they are attached to form a 3- to 6-membered cycloalkyl or heterocyclic ring;
R 4 is hydrogen or methyl;
R 5 is pyrazolyl optionally independently substituted with 1 to 3 substituents chosen from C 1 -C 6 alkyl (which is optionally substituted with 1 to 3 halogen atoms or with a heterocyclyl group), C 1 -C 6 alkoxy (which is optionally substituted with 1 to 3 halogen atoms), C 1 -C 6 cycloalkyl, heterocyclyl, phenoxy, halogen, cyano, dimethylaminoalkyl, phenyl (which is optionally substituted with 1 to 2 halogen atoms or C 1 -C 4 alkyl optionally substituted with halogen), thienyl (which is optionally substituted with 1 to 2 halogen atoms or C 1 -C 4 alkyl optionally substituted with halogen), and pyridinyl (which is optionally substituted with 1 to 2 C 1 -C 4 alkyl optionally substituted with halogen);
wherein R 2 and R 3 , together with the carbon atom to which they are attached, do not form a cyclopropyl ring when R 5 is 1-phenyl 5-pyrazolyl, and R 1 is a phenyl, 4-chlorophenyl or 4-methylphenyl;
or a tautomer or pharmaceutically acceptable salt thereof.
2. The compound according to claim 1 wherein,
R 1 is a phenyl optionally independently substituted with 1 to 3 substituents chosen from C 1 -C 6 alkyl (which is optionally substituted with 1 to 3 halogen atoms), C 1 -C 6 cycloalkyl, C 1 -C 6 alkoxy (which is optionally substituted with 1 to 3 halogen atoms), C 1 -C 6 alkylthio, C 1 -C 6 alkylsulfonyl, C 1 -C 6 alkoxycarbonyl, C 1 -C 6 alkylamino, C 3 -C 6 cycloalkylamino, C 1 -C 6 dialkylamino, C 1 -C 6 alkylaminocarbonyl, acylamino, C 1 -C 6 dialkylaminocarbonyl, hydroxyl, halogen, cyano, nitro, oxo, phenyl, pyrazolyl, morpholinyl and azetidinyl;
R 2 and R 3 are independently hydrogen, methyl, ethyl, n-propyl, isopropyl, isobutyl, tert-butyl, or R 2 and R 3 together with the carbon they are attached to form cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or tetrahydropyranyl ring;
R 4 is hydrogen;
R 5 is pyrazolyl, optionally independently substituted with 1 to 3 substituents chosen from C 1 -C 6 alkyl (which is optionally substituted with 1 to 3 halogen atoms or piperidinyl), C 1 -C 6 alkoxy (which is optionally substituted with 1 to 3 halogen atoms), C 1 -C 6 cycloalkyl, tetrahydropyranyl, phenoxy, halogen, cyano, dimethylaminoalkyl, phenyl (which is optionally substituted with 1 to 2 halogen atoms, C 1 -C 4 alkyl optionally substituted with halogen), thienyl (which is optionally substituted with 1 to 2 halogen atoms, C 1 -C 4 alkyl optionally substituted with halogen), and pyridinyl (which is optionally substituted with 1 to 2 C 1 -C 4 alkyl optionally substituted with halogen).
3. The compound according to claim 2 wherein,
R 1 is a phenyl optionally independently substituted with 1 to 3 substituents chosen from C 1 -C 6 alkyl (which is optionally substituted with 1 to 3 halogen atoms), C 1 -C 6 cycloalkyl, C 1 -C 6 alkoxy (which is optionally substituted with 1 to 3 halogen atoms), C 1 -C 6 alkylthio, C 1 -C 6 alkylsulfonyl, C 1 -C 6 alkoxycarbonyl, C 1 -C 6 alkylaminocarbonyl, carboxyamino, C 1 -C 6 dialkylaminocarbonyl, hydroxyl, halogen, cyano, nitro, phenyl, pyrazolyl, morpholinyl and azetidinyl;
R 2 and R 3 are independently hydrogen, methyl, ethyl, n-propyl, isopropyl, isobutyl, tert-butyl, or R 2 and R 3 together with the carbon they are attached to form cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or tetrahydropyranyl ring;
R 4 is hydrogen;
R 5 is pyrazolyl, optionally independently substituted with 1 to3 substituents chosen from C 1 -C 6 alkyl (which is optionally substituted with 1 to 3 halogen atoms), C 1 -C 6 alkoxy (which is optionally substituted with 1 to 3 halogen atoms), C 1 -C 6 cycloalkyl, tetrahydropyranyl, phenoxy, halogen, cyano, dimethylaminoalkyl, phenyl (which is optionally substituted with 1 to 2 halogen atoms, C 1 -C 4 alkyl optionally substituted with halogen), thienyl (which is optionally substituted with 1 to 2 halogen atoms, C 1 -C 4 alkyl optionally substituted with halogen), and pyridinyl (which is optionally substituted with 1 to 2 C 1 -C 4 alkyl optionally substituted with halogen).
4. The compound according to claim 3 wherein,
R 1 is a phenyl, optionally independently substituted with 1 to 3 substitutents chosen from methyl, ethyl, n-propyl, isopropyl, cyclopropyl, tert-butyl, trifluoromethyl, trifluoroethyl, methoxy, trifluoromethoxy, methylsulfonyl, fluoro, chloro, bromo, cyano nitro, morpholine, and azetidine;
R 2 and R 3 are independently hydrogen, methyl, isopropyl, tert-butyl, or R 2 and R 3 together with the carbon they are attached to form cyclopropyl or cyclobutyl, ring;
R 4 is hydrogen;
R 5 is pyrazolyl optionally independently substituted with 1 to 3 substituents chosen from methyl, ethyl, cyclopropyl, tert-butyl, trifluoromethyl, phenoxy, chloro, phenyl (which is optionally substituted with chloro), thienyl, and pyridinyl.
5. A compound chosen from
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(4-chloro-benzenesulfonyl)-2-methyl-propionamide,
2-(4-Chloro-benzenesulfonyl)-2-methyl-N-(2-methyl-5-phenyl-2H-pyrazol-3-yl)-propionamide,
2-(4-Chloro-benzenesulfonyl)-N-(5-cyclopropyl-2-methyl-2H-pyrazol-3-yl)-2-methyl-propionamide,
2-(4-Chloro-benzenesulfonyl)-2-methyl-N-(5-methyl-2-phenyl-2H-pyrazol-3-yl)-propionamide,
2-(4-Chloro-benzenesulfonyl)-N-(2,5-dimethyl-2H-pyrazol-3-yl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-3-methyl-2-(4-trifluoromethyl-benzenesulfonyl)-butyramide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(4-chloro-2-fluoro-benzenesulfonyl)-2-methyl-propionamide,
2-(4-Bromo-benzenesulfonyl)-N-(5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(4-cyano-benzenesulfonyl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(3-fluoro-4-methyl-benzenesulfonyl)-2-methyl-propionamide,
4-(4-Trifluoromethyl-benzenesulfonyl)-tetrahydro-pyran-4-carboxylic acid (5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-amide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(3-fluoro-4-methoxy-benzenesulfonyl)-2-methyl-propionamide,
N-(5-tert-Butyl-2H-pyrazol-3-yl)-2-(4-chloro-benzenesulfonyl)-2-methyl-propionamide,
1-(4-Trifluoromethyl-benzenesulfonyl)-cyclopropanecarboxylic acid (5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-amide,
2-(4-Chloro-benzenesulfonyl)-N-(5-cyclohexyl-2-methyl-2H-pyrazol-3-yl)-2-methyl-propionamide,
2-(4-Chloro-benzenesulfonyl)-N-(5-cyclopentyl-2-methyl-2H-pyrazol-3-yl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-methyl-2-(toluene-4-sulfonyl)-propionamide,
2-Benzenesulfonyl-N-(5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-2-methyl-propionamide,
2-Benzenesulfonyl-2-methyl-N-(2-methyl-5-phenyl-2H-pyrazol-3-yl)-propionamide,
1-(4-Chloro-benzenesulfonyl)-cyclopropanecarboxylic acid (5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-amide,
1-(4-Chloro-benzenesulfonyl)-cyclopropanecarboxylic acid (5-tert-butyl-2H-pyrazol-3-yl)-amide
1-(4-Chloro-benzenesulfonyl)-cyclopropanecarboxylic acid (2-methyl-5-phenyl-2H-pyrazol-3-yl)-amide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(3-fluoro-benzenesulfonyl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(2-fluoro-benzenesulfonyl)-2-methyl-propionamide,
N-(5-tert-Butyl-2H-pyrazol-3-yl)-2-(2-fluoro-benzenesulfonyl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(2-fluoro-4-methyl-benzenesulfonyl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(4-cyano-2-fluoro-benzenesulfonyl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(4-fluoro-benzenesulfonyl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(2,5-difluoro-benzenesulfonyl)-2-methyl-propionamide,
2-(4-Chloro-benzenesulfonyl)-N-(2,4-dimethyl-5-phenyl-2H-pyrazol-3-yl)-2-methyl-propionamide,
2-(4-Chloro-benzenesulfonyl)-N-(5-isopropyl-2-methyl-2H-pyrazol-3-yl)-2-methyl-propionamide,
2-(2,4-Difluoro-benzenesulfonyl)-2-methyl-N-(2-methyl-5-phenyl-2H-pyrazol-3-yl)-propionamide,
N-(5-Cyclopropyl-2-methyl-2H-pyrazol-3-yl)-2-(2,4-difluoro-benzenesulfonyl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(2,4-difluoro-benzenesulfonyl)-2-methyl-propionamide,
2-(4-Methoxy-benzenesulfonyl)-2-methyl-N-(2-methyl-5-phenyl-2H-pyrazol-3-yl)-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(4-methoxy-benzenesulfonyl)-2-methyl-propionamide,
2-(4-Methoxy-benzenesulfonyl)-2-methyl-N-(2-methyl-5-thiophen-2-yl-2H-pyrazol-3-yl)-propionamide,
2-methyl-N-(1-methyl-3-phenyl-1H-pyrazol-5-yl)-2-{[4-(methylsulfonyl)phenyl]sulfonyl}propanamide,
N-(3-tert-butyl-1-methyl-1H-pyrazol-5-yl)-2-methyl-2-{[4-(methylsulfonyl)phenyl]sulfonyl}propanamide and
N-(1,4-dimethyl-3-phenyl-1H-pyrazol-5-yl)-2-[(4-methoxyphenyl)sulfonyl]-2-methylpropanamide,
N-(5-sec-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(4-chloro-benzenesulfonyl)-2-methyl-propionamide,
or a tautomer or pharmaceutically acceptable salt thereof.
6. A compound chosen from
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(4-chloro-benzenesulfonyl)-2-methyl-propionamide,
2-(4-Chloro-benzenesulfonyl)-2-methyl-N-(2-methyl-5-phenyl-2H-pyrazol-3-yl)-propionamide,
2-(4-Chloro-benzenesulfonyl)-2-methyl-N-(2-methyl-5-thiophen-2-yl-2H-pyrazol-3-yl)-propionamide,
2-(4-Chloro-benzenesulfonyl)-N-(5-cyclopropyl-2-methyl-2H-pyrazol-3-yl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(4-chloro-2-fluoro-benzenesulfonyl)-2-methyl-propionamide,
2-(4-Bromo-benzenesulfonyl)-N-(5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(4-cyano-benzenesulfonyl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(3-fluoro-4-methyl-benzenesulfonyl)-2-methyl-propionamide,
2-(4-Chloro-2-fluoro-benzenesulfonyl)-2-methyl-N-(2-methyl-5-phenyl-2H-pyrazol-3-yl)-propionamide,
4-(4-Trifluoromethyl-benzenesulfonyl)-tetrahydro-pyran-4-carboxylic acid (5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-amide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(3-fluoro-4-methoxy-benzenesulfonyl)-2-methyl-propionamide,
1-(4-Trifluoromethyl-benzenesulfonyl)-cyclopropanecarboxylic acid (5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-amide,
2-(4-Chloro-benzenesulfonyl)-N-(5-cyclohexyl-2-methyl-2H-pyrazol-3-yl)-2-methyl-propionamide,
2-(4-Chloro-benzenesulfonyl)-N-(5-cyclopentyl-2-methyl-2H-pyrazol-3-yl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-methyl-2-(toluene-4-sulfonyl)-propionamide,
2-Methyl-N-(2-methyl-5-phenyl-2H-pyrazol-3-yl)-2-(toluene-4-sulfonyl)-propionamide,
1-(4-Chloro-benzenesulfonyl)-cyclopropanecarboxylic acid (5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-amide,
1-(4-Chloro-benzenesulfonyl)-cyclopropanecarboxylic acid (5-tert-butyl-2H-pyrazol-3-yl)-amide
1-(4-Chloro-benzenesulfonyl)-cyclopropanecarboxylic acid (2-methyl-5-phenyl-2H-pyrazol-3-yl)-amide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(3-fluoro-benzenesulfonyl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(2-fluoro-benzenesulfonyl)-2-methyl-propionamide,
N-(5-tert-Butyl-2H-pyrazol-3-yl)-2-(2-fluoro-benzenesulfonyl)-2-methyl-propionamide
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(2-fluoro-4-methyl-benzenesulfonyl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(4-cyano-2-fluoro-benzenesulfonyl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(4-fluoro-benzenesulfonyl)-2-methyl-propionamide,
2-(4-Chloro-benzenesulfonyl)-N-(2,4-dimethyl-5-phenyl-2H-pyrazol-3-yl)-2-methyl-propionamide,
2-(4-Chloro-benzenesulfonyl)-N-(5-isopropyl-2-methyl-2H-pyrazol-3-yl)-2-methyl-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(2,4-difluoro-benzenesulfonyl)-2-methyl-propionamide,
2-(4-Methoxy-benzenesulfonyl)-2-methyl-N-(2-methyl-5-phenyl-2H-pyrazol-3-yl)-propionamide,
N-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(4-methoxy-benzenesulfonyl)-2-methyl-propionamide,
2-(4-Methoxy-benzenesulfonyl)-2-methyl-N-(2-methyl-5-thiophen-2-yl-2H-pyrazol-3-yl)-propionamide and
N-(5-sec-Butyl-2-methyl-2H-pyrazol-3-yl)-2-(4-chloro-benzenesulfonyl)-2-methyl-propionamide,
or a tautomer or pharmaceutically acceptable salt thereof.
7. A pharmaceutical composition comprising a therapeutically effective amount of a compound according to claim 1 .
8. A method for the treatment of a CB2 receptor-mediated disease or condition in an animal subject comprising administering to said animal subject in need of such treatment a therapeutically effective dose of the compound according to claim 1 , wherein the CB2 receptor-mediated disease or condition is pain.
9. The method according to claim 8 wherein said CB2 receptor-mediated disease or condition is selected from the group consisting of acute pain, visceral pain, neuropathic pain, inflammatory pain, nociceptive pain, cancer pain, and headache.