IP Library › Granted Patent US 7,572,785

Granted Patent B2

US 7,572,785 · App. 11/265,850 · Granted Aug 11, 2009

Substituted imidazoles as cannabinoid receptor modulators

View Patent ↗

Loading inventors, assignments & file history…

Monitor This Case

Get email alerts when status or documents change.

Order Certified Copies

Most orders are placed with the USPTO same day — all within 24 business hours.

Order via The Patent Place →

Pre-filled with this patent's details

Quick Facts

Patent No.: US 7,572,785
App. No.: 11/265,850
Granted: Aug 11, 2009
Kind: B2

External Links

USPTO Patent Center↗ Full Patent PDF↗

Abstract

The use of compounds of the present invention as antagonists and/or inverse agonists of the Cannabinoid-1 (CB1) receptor particularly in the treatment, prevention and suppression of diseases mediated by the Cannabinoid-1 (CB1) receptor. The invention is concerned with the use of these novel compounds to selectively antagonize the Cannabinoid-1 (CB1) receptor. As such, compounds of the present invention are useful as psychotropic drugs in the treatment of psychosis, memory deficits, cognitive disorders, migraine, neuropathy, neuro-inflammatory disorders including multiple sclerosis and Guillain-Barre syndrome and the inflammatory sequelae of viral encephalitis, cerebral vascular accidents, and head trauma, anxiety disorders, stress, epilepsy, Parkinson's disease, and schizophrenia. The compounds are also useful for the treatment of substance abuse disorders, particularly to opiates, alcohol, and nicotine. The compounds are also useful for the treatment of obesity or eating disorders associated with excessive food intake and complications associated therewith. Novel compounds of structural formula (I) are also claimed.

Claims (102)

1. A compound of structural formula (I):

or a pharmaceutically acceptable salt thereof, wherein:

R 1 is selected from:

(1) hydrogen

(2) C 1-10 alkyl,

(3) C 2-10 alkenyl,

(4) C 2-10 alkynyl,

(5) cycloalkyl,

(6) cycloalkyl-C 1-10 alkyl,

wherein alkyl, alkenyl, alkynyl, and cycloalkyl, are optionally substituted with one to four substituents independently selected from C 1-4 alkoxy, amino, and R a ;

R 2 is selected from:

(1) —OR d , and

(2) —NR d R e ;

Ar 1 and Ar 2 are each independently selected from:

(1) phenyl,

(2) 4-chlorophenyl,

(3) 4-methylphenyl, and

(4) 2,4-dichlorophenyl;

each R a is independently selected from:

(1) —OR d ,

(2) —NR d S(O) m R e ,

(3) —S(O) m R d ,

(4) —SR d ,

(5) —S(O) m NR d R e ,

(6) —NR d R e ,

(7) —O(CR f R g ) n NR d R c ,

(8) —CO 2 R d ,

(9) —CO 2 (CR f R g ) n CONR d R e ,

(10) —OC(O)R d ,

(11) —C(O)NR d R e ,

(12) —NR d C(O)R e ,

(13) —OC(O)NR d R e ,

(14) —NR d C(O)OR e ,

(15) —NR d C(O)NR d R e , and

(16) —CR d (N—OR e );

wherein R d is selected from piperidinyl, morpholinyl, pyrrolidinyl, azepinyl, tetrahydropyranyl and 2,2-dimethyl tetrahydropyranyl; R e is selected from hydrogen and methyl; or R d and R e together with the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, or morpholinyl ring;

R f and R g are independently selected from hydrogen, C 1-10 alkyl, cycloalkyl; and

cycloalkyl-C 1-10 alkyl;

wherein cycloalkyl is selected from: cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and cycloheptyl;

m is selected from 1 and 2; and

n is selected from 1, 2, and 3.

2. The compound according to claim 1 , wherein:

R 1 is C 1-10 alkyl;

R 2 is as in claim 1 ;

Ar 1 is 4-chlorophenyl, and Ar 2 is 2,4-dichlorophenyl; and

R d is selected from piperidinyl, morpholinyl, and pyrrolidinyl; R e is selected from hydrogen and methyl; or R d and R e together with the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, or morpholinyl ring;

or a pharmaceutically acceptable salt thereof.

3. The compound according to claim 2 , wherein:

R 1 is methyl;

R 2 is —NR d R e ;

Ar 1 is 4-chlorophenyl, and Ar 2 is 2,4-dichlorophenyl;

R d is 1-piperidinyl;

or a pharmaceutically acceptable salt thereof.

4. A compound selected from:

(1) N-(piperidin-1-yl)-4,5-diphenyl-1-methylimidazole-2-carboxamide,

(2) 2-(piperidin-1-ylcarbonyl)-4,5-diphenyl-1-methylimidazole,

(3) N-(morpholin-4-yl)-4,5-diphenyl-1-methylimidazole-2-carboxamide,

(4) N-(piperidin-1-yl)-4,5-di-(4-methylphenyl)-1-methylimidazole-2-carboxamide,

(5) 2-(piperidin-1-ylcarbonyl)-4,5-di-(4-methylphenyl)-1-methylimidazole,

(6) N-(morpholin-4-yl)-4,5-di-(4-methylphenyl)-1-methylimidazole-2-carboxamide,

(7) 2-(pyrrolidin-1-ylcarbonyl)-4,5-di-(4-methylphenyl)-1-methylimidazole,

(8) N-(piperidin-1-yl)-4,5-di-(4-chlorophenyl)-1-methylimidazole-2-carboxamide,

(9) 2-(piperidin-1-ylcarbonyl)-4,5-di-(4-chlorophenyl)-1-methylimidazole, N-(morpholin-1-yl)-4,5-di-(4-chlorophenyl)-1-methylimidazole-2-carboxamide,

(11) N-(piperidin-1-yl)-4,5-di-(4-chlorophenyl)imidazole-2-carboxamide, N-(piperidin-1-yl)-4,5-di-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxamide,

(13) N-(piperidin-1-yl)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxamide,

(14) N-(piperidin-1-yl)-4-(2,4-dichlorophenyl)-5-(4-chlorophenyl)-1-methylimidazole-2-carboxamide,

(15) N-(morpholin-4-yl)-4-(2,4-dichlorophenyl)-5-(4-chlorophenyl)-1-methylimidazole-2-carboxamide,

(16) N-(piperidin-1-yl)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-ethylimidazole-2-carboxamide,

(17) N-(piperidin-1-yl)-5-(4-chlorophenyl)-4-(2,4-dichlorophenyl)-1-methyl-imidazole-2-carboxamide,

(18) N-(pyrrolidin-1-yl)-5-(4-chlorophenyl)-4-(2,4-dichlorophenyl)-1-methyl-imidazole-2-carboxamide,

(19) N-(azepin-1-yl)-5-(4-chlorophenyl)-4-(2,4-dichlorophenyl)-1-methyl-imidazole-2-carboxamide,

(20) N-(tetrahydropyran-4-yl)-4-(2,4-dichlorophenyl)-5-(4-chlorophenyl)-1-methylimidazole-2-carboxamide,

(21) N-(2,2-dimethyl-tetrahydropyran-4-yl)-4-(2,4-dichlorophenyl)-5-(4-chlorophenyl)-1-methylimidazole-2-carboxamide,

(22) N-(piperidin-1-yl)-5-(4-chlorophenyl)-4-(2,4-dichlorophenyl)-1-ethyl-imidazole-2-carboxamide,

(23) N-(piperidin-1-yl)-5-(4-chlorophenyl)-4-(2,4-dichlorophenyl)-1-(1-methyl)ethyl-imidazole-2-carboxamide,

(24) N-(piperidin-1-yl)-5-(4-chlorophenyl)-4-(2,4-dichlorophenyl)-1-(1,1-dimethyl)ethyl-imidazole-2-carboxamide,

(25) N-(piperidin-1-yl)-5-(4-chlorophenyl)-4-(2,4-dichlorophenyl)-1-(2-dimethylamino)ethyl-imidazole-2-carboxamide,

(26) N-(piperidin-1-yl)-5-(4-chlorophenyl)-4-(2,4-dichlorophenyl)-1-propyl-imidazole-2-carboxamide,

(27) N-(piperidin-1-yl)-5-(4-chlorophenyl)-4-(2,4-dichlorophenyl)-1-butyl-imidazole-2-carboxamide,

(28) N-(piperidin-1-yl)-5-(4-chlorophenyl)-4-(2,4-dichlorophenyl)-1-(2-methoxy)ethyl-imidazole-2-carboxamide, and

(29) N-(piperidin-1-yl)-4-(2-chlorophenyl)-5-(4-chlorophenyl)-1-methyl-imidazole-2-carboxamide, and pharmaceutically acceptable salts thereof.

5. The compound according to claim 4 selected from: