首页> 外国专利> Process for the preparation of novel 7 beta-(fluorinated methylthio)-acetamido-7 alpha-methoxy-3-(1-(2- hydroxyalkyl)-1H-tetrazol-5-yl)thiomethyl-1-dethia-1-oxa- 3-cephem-4-carboxylic acid derivatives

Process for the preparation of novel 7 beta-(fluorinated methylthio)-acetamido-7 alpha-methoxy-3-(1-(2- hydroxyalkyl)-1H-tetrazol-5-yl)thiomethyl-1-dethia-1-oxa- 3-cephem-4-carboxylic acid derivatives

机译:制备新型7β-(氟化甲硫基)-乙酰氨基-7α-甲氧基-3-(1-(2-羟烷基)-1H-四唑-5-基)硫基甲基1-deia-1-oxa-的方法3-头孢-4-羧酸衍生物

摘要

7 Beta-(fluorinated methylthio)-acetamido-7 alpha-methoxy- 3-(1-(2-hydroxyalkyl)-1H-tetrazol-5-yl)-thiomethyl-1- dethia-1-oxa-3-cephem-4-carboxylic acid derivatives of the general formula I in which R is FCH2- or F2CH-, R1 is optionally protected 2-hydroxyalkyl, and R2 is hydrogen, a light metal atom or a carboxyl protective group, have antibacterial activity. They are obtained by reacting a 7 beta-(fluorinated methylthio)-acetamido-7 alpha-methoxy-3-halomethyl-1- dethia-1-oxa-3-cephem-4-carboxylic acid derivative with 1- (2-hydroxyalkyl)-1H-tetrazol-5-ylthiol. IMAGE
机译:7β-(氟化甲硫基)-乙酰胺基7α-甲氧基-3-(1-(2-羟烷基)-1H-四唑-5-基)-硫代甲基-1- dethia-1-oxa-3-cephem-4通式I的通式-I的羧酸衍生物具有抗菌活性,其中R是FCH 2-或F 2 CH-,R 1是任选被保护的2-羟基烷基,并且R 2是氢,轻金属原子或羧基保护基。它们是通过7-β-(氟化甲硫基)-乙酰氨基-7α-甲氧基-3-卤代甲基-1-二硫-1-氧杂-3- Cephem-4-羧酸衍生物与1-(2-羟烷基)反应制得的。 -1H-四唑-5-基硫醇。 <图像>

著录项

  • 公开/公告号AT389699B

    专利类型

  • 公开/公告日1990-01-10

    原文格式PDF

  • 申请/专利权人 SHIONOGI & CO. LTD.;

    申请/专利号AT19860002564

  • 发明设计人 TSUJI TERUJI;SATO HISAO;HAMASHIMA YOSHIO;

    申请日1986-09-25

  • 分类号C07D498/04;

  • 国家 AT

  • 入库时间 2022-08-22 06:16:46

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号