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Piperidine derivatives as 5-HT4 receptor antagonists (Piperidine Derivatives as 5-HT4 Receptor Antagonists)
Piperidine derivatives as 5-HT4 receptor antagonists (Piperidine Derivatives as 5-HT4 Receptor Antagonists)
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机译:哌啶衍生物作为5-HT4受体拮抗剂(哌啶衍生物作为5-HT4受体拮抗剂)
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摘要
The present invention also relates to the compounds of the general formula (I) and pharmaceutically acceptable salts thereof and the compounds of the general formula (I) or the pharmaceutically acceptable salts or the salts thereof wherein the CO-Y bond is substituted by a heterocyclic bioequivalent I) and for use as pharmaceutical preparations in the treatment of gastrointestinal tract disorders, cardiovascular disorders and CNS disorders.;X-CO-Y-Z (1);Wherein X is a monocyclic or polycyclic aromatic group and Y is O or NH; Z is the following formula;(Wherein,-(CH2)nOneIs asked for carbon; nOneIs 0, 1, 2, 3 or 4; p is 0, 1, 2 or 3; RaR7Substituted straight chain or branched chain alkylene having 1 to 6 carbon atoms, wherein R7Is a 9-or 10-membered fused bicyclic heteroaryl linked via a 3-to 8-membered cycloalkyl, a 3-to 8-membered heterocyclyl, a 5-or 6-membered monocyclic heptaloaryl or a carbon, or R7C2-7Alkoxycarbonyl or a secondary or tertiary hydroxy substituted C1-6Alkyl; R6Is hydrogen or C1-6Alkyl.
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机译:本发明还涉及通式(I)的化合物及其药学上可接受的盐,以及其中CO-Y键被杂环取代的通式(I)的化合物或其药学上可接受的盐或它们的盐。 X-CO-YZ(1);其中X为单环或多环芳族基团,Y为O或NH;(C)生物等效物I)并用作药物制剂,用于治疗胃肠道疾病,心血管疾病和CNS疾病。 Z是下式;(其中,-(CH 2 Sub>) n Sub> 一个 Sup>被要求碳; n 一个 Sup >为0、1、2、3或4; p为0、1、2或3; R a Sup> R 7 Sub>具有1至1的取代的直链或支链亚烷基6个碳原子,其中R 7 Sub>是经由3至8元环烷基,3至8元杂环基,5或6键连接的9元或10元稠合双环杂芳基元单环七芳基或碳,或R 7 Sub> C 2-7 Sub>烷氧羰基或仲或叔羟基取代的C 1-6 Sub>烷基; R 6 Sub>是氢或C 1-6 Sub>烷基。
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