Tetrazolyl-substituted quinuclidines as substance P antagonists

摘要

This invention provides a compound of the formula: and its pharmaceutically acceptable salts, wherein R<1> is halo, C1-C6 alkyl, halo C1-C6 alkyl, C1-C6 alkoxy or halo C1-C6 alkoxy; R<2> is hydrogen, C1-C6 alkyl, halo C1-C6 alkyl, C1-C6 alkyl-S-, C1-C6 alkyl-SO-, C1-C6 alkyl-SO2-, cyclopropyl, phenyl, -NH2, -NH(CH3), -NHC(=O)CH3, -N(CH3)2, - N(C2H5)2 or -CH2C(=O)CF3; Ar<1> and Ar<2> are independently phenyl, halophenyl or thienyl; X is NH, O or S; and Y is hydrogen, -COOR<3> or -CONR<4>R<5>, wherein R<3>, R<4> and R<5> are independently hydrogen or C1-C6 alkyl. These compounds are useful as analgesics or anti-inflammatory agents, or in the treatment of allergic disorders, angiogenesis, CNS disorders, emesis, gastrointestinal disorders, sunburn, urinary incontinence, or diseases, disorders or adverse conditions caused by Helicobacter pylori, or the like, in a mammalian subject, especially human, especially as analgesics or anti-inflammatory agents in the periphery.