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Process for preparing of novel antimicrobial -5- (n-heterosubstituted amino) quinolones

机译:新型抗菌药物-5-(正杂取代氨基)喹诺酮类药物的制备方法

摘要

Antimicrobial 5-(N-heterosubstituted amino) quinolone compounds of general formula (I), wherein (1) R1, R2 and R3 form any of a variety of quinolone and related heterocyclic structures similar to those known in the art to have antimicrobial activity; and (2) (a) R4 and R5 are, independently, hydrogen; lower alkyl; cycloalkyl; heteroalkyl; or -C(=O)-X-R8, where X is a covalent bond, N, O, or S, and R8 is lower alkyl, lower alkenyl, arylalkyl, a carbocyclic ring, or a heterocyclic ring; or (b) R4 and R5 together comprise a heterocyclic ring that includes the nitrogen to which they are bonded; and pharmaceutically-acceptable salts and biohydrolyzable esters thereof, and solvates thereof.
机译:通式(I)的抗微生物的5-(N-杂取代氨基)喹诺酮化合物,其中(1)R 1,R 2和R 3形成多种喹诺酮及其相关杂环结构中的任何一种本领域已知具有抗微生物活性; (2)(a)R 4和R 5独立地为氢。低级烷基;环烷基杂烷基或-C(= O)-X-R 8,其中X是共价键,N,O或S,并且R 8是低级烷基,低级烯基,芳基烷基,碳环或杂环; (b)R 4和R 5一起构成杂环,该杂环包括与它们键合的氮;及其药学上可接受的盐和生物水解酯,及其溶剂化物。

著录项

  • 公开/公告号EG20543A

    专利类型

  • 公开/公告日1999-07-31

    原文格式PDF

  • 申请/专利权人 THE PROCTOR & GAMBLE CO.;

    申请/专利号EG19930000686

  • 发明设计人 DEMUTH THOMAS PROSSER JR;

    申请日1993-01-30

  • 分类号C07D215/56;C07D401/04;A61K31/47;

  • 国家 EG

  • 入库时间 2022-08-22 02:27:38

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