首页> 外国专利> Method for preparing acid compounds (6 - 7 - 1,2 dihydro - phenyl - 2 - 3 - oxopiridina carbonylamino) - fenilacetamino - 3 - methyl - 3-cephem-4-carboxylic - carboxylic acid and its Salts

Method for preparing acid compounds (6 - 7 - 1,2 dihydro - phenyl - 2 - 3 - oxopiridina carbonylamino) - fenilacetamino - 3 - methyl - 3-cephem-4-carboxylic - carboxylic acid and its Salts

机译:制备酸化合物的方法(6-7-1,2-二氢-苯基-2-3-氧代氧化吡啶基羰基氨基)-苯乙酰胺基氨基-3-甲基-3-苯甲基-4-羧酸-羧酸及其盐

摘要

Cephalosporin compounds, intermediate compounds therefor, and processes for preparation thereof are described; the compounds have the formula (I) IMAGE (I) IMAGE wherein R1 and R2 can each represent hydrogen, a hydroxyl group, a lower alkoxy group, or a substituted or unsubstituted phenylalkoxy group; R3 represents hydrogen or a lower alkyl group; R4 represents hydrogen or a hydroxyl group; and R5 represents IMAGE +TR IMAGE wherein R6 is hydrogen, a lower alkyl group, an aminoalkyl group, an aminoaralkyl group, a -(CH2)n-SO3Na group, or a -(CH2)n-COR9 group [wherein R9 is a hydroxyl group, an OM group (wherein M is an alkali metal), an alkoxy group, or an IMAGE group, (wherein R10 and R11, which may be the same or different, can represent hydrogen or an alkyl group), and n is 0 or an integer of from 1 to 4]; R7 is hydrogen, a lower alkyl group, an amino group, or a substituted or unsubstituted aryl group; and R8 represents hydrogen or a lower alkyl group; or, a pharmaceutically acceptable salt thereof.
机译:描述了头孢菌素化合物,其中间体化合物及其制备方法。所述化合物具有式(I)<图像>(I)<图像>,其中R 1和R 2可以分别表示氢,羟基,低级烷氧基或取代或未取代的苯基烷氧基。 R3代表氢或低级烷基; R4代表氢或羟基; [化5] [式中,R5表示氢,低级烷基,氨基烷基,氨基芳烷基,-(CH2)n-SO3Na或-(CH2)n-COR9 [其中R9是羟基,OM基团(其中M是碱金属),烷氧基或基团(其中R10和R11可以相同或不同,可以表示氢或烷基)组),n为0或1到4的整数]; R7是氢,低级烷基,氨基或取代或未取代的芳基; R 8表示氢或低级烷基。或其药学上可接受的盐。

著录项

  • 公开/公告号AR227452A1

    专利类型

  • 公开/公告日1982-10-29

    原文格式PDF

  • 申请/专利权人 MEIJI SEIKA KAISHA LTD;

    申请/专利号AR19810287751

  • 发明设计人

    申请日1981-12-10

  • 分类号C07D501/36;

  • 国家 AR

  • 入库时间 2022-08-22 13:56:58

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