| abstract |
Formula I: Wherein R 1 is selected from hydrogen, halogen, hydroxyl, and C 1-4 alkoxy; R 2 is selected from hydrogen, halogen, hydroxyl, and C 1-4 alkoxy; R 3 is C 1-4 alkyl R4 is aryl substituted with a group selected from OSO 2 NH 2 , NHCONH 2 , NHSO 2 NH 2 , NHSO 2 C 1-4 alkyl, and CONH 2 ; and n is 0 or Wherein N- (1-benzylpiperidin-4-yl) -N-methyl-4- (4- (sulfamoylamino) phenyl) -1H-imidazole-1- The above compound which is not carboxamide or N- (1-benzylpiperidin-4-yl) -N-methyl-4- (3- (methylsulfonamido) phenyl) -1H-imidazole-1-carboxamide or a pharmaceutically acceptable salt thereof Salt. The present compounds can also be used as inhibitors of fatty acid amide hydrolase. |