申请人:BOC, Inc.
公开号:US04994471A1
公开(公告)日:1991-02-19
This invention pertains to novel N-aryl-N-[N-substituted 3-alkoxy-4-piperidinyl]amides useful as analgesics, and methods of administering analgesia, which comprises the systemic administration to mammals of such compounds, and pharmaceutical compositions containing such compounds, wherein the novel compounds have the general formula: ##STR1## including optically active isomeric forms, cis/trans isomeric forms and the pharmaceutically acceptable acid addition salts therof, wherein: R is an aryl group selected from the group consisting of phenyl and substituted phenyl, wherein the substituents on the phenyl group are independently selected from the group consisting of halogen, lower-alkyl, lower-alkoxy, and combinations thereof; R.sub.1 is an alkyl group selected from the group consisting of lower-alkyl, lower-alkenyl, and lower-alkoxy lower-alkyl, each alkyl group having from 1 to 6 carbon atoms; R.sub.2 is a member selected from the group consisting of phenyl lower-alkyl, thienyl lower-alkyl, pyrazolyl lower-alkyl, tetrazolyl lower-alkyl, 4,5-dihydro-5-oxo-1H-tetrazolyl lower-alkyl, 1,3-dihydro-1,3-dioxo-2H-isoindolyl lower-alkyl, and 2,3-dihydro-2-oxo-1H-benzimidazolyl lower-alkyl; and R.sub.3 is a member selected from the group consisting of hydrogen, lower-alkyl and lower-alkyl aryl.
本发明涉及一种新型的N-芳基-N-[N-取代3-烷氧基-4-
哌啶基]酰胺,用作镇痛剂,以及给哺乳动物系统性地给予这种化合物的镇痛方法和含有这种化合物的制药组合物,其中这种新型化合物具有以下通式:##STR1## 包括光学活性异构体形式,顺反异构体形式和其药学上可接受的酸加成盐,其中:R是从苯基和取代苯基组成的群体中选择的芳基基团,其中苯基上的取代基是独立地从卤素、低烷基、低烷氧基和它们的组合中选择的;R.sub.1是从低烷基、低烯基和低烷氧基低烷基组成的群体中选择的烷基基团,每个烷基含有1至6个碳原子;R.sub.2是从苯基低烷基、
噻吩基低烷基、
吡唑基低烷基、
四唑基低烷基、4,
5-二氢-5-氧代-
1H-四唑基低烷基、1,3-二氢-1,3-二氧代-
2H-异吲哚基低烷基和
2,3-二氢-2-氧代-1H-
苯并咪唑基低烷基中选择的成员;以及R.sub.3是从氢、低烷基和低烷基芳基中选择的成员。