节点文献

盐酸头孢甲肟的合成

Synthesis of Cefmenoxime Hydrochloride

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 白国义李新娟彭洪伟贾春伟王海龙

【Author】 BAI Guo-yi,LI Xin-juan,PENG Hong-wei,JIA Chun-wei,WANG Hai-long (Key Laboratory of Chemical Biology of Hebei Province,College of Chemistry and Environmental Science,Hebei University,Baoding 071002,Hebei,China)

【机构】 河北大学化学与环境科学学院河北省化学生物重点实验室

【摘要】 以7-氨基头孢烷酸(7-ACA)为原料,通过两条路线对第三代头孢菌素——盐酸头孢甲肟的合成进行了系统考察。实验证明,7-ACA先在C-3位与5-巯基-1-甲基-1H-四氮唑(MMT)反应生成3-(1-甲基-1H-四氮唑-5-基)硫甲基-7-氨基头孢霉烷酸(7-ACT),再在C-7位和MAEM反应合成头孢甲肟的路线(摩尔收率为86%)优于先进行7-ACA的C-7位改造再进行C-3位改造的合成路线(摩尔收率为69%)。溶剂对反应的摩尔收率有较大影响,以二氯甲烷为溶剂时的反应效果最佳;同时证明超声能够显著缩短反应时间。

【Abstract】 The third generation cephalosporin of cefmenoxime hydrochloride was synthesized by two routes using 7-ACA as the raw material.The route,in which 7-ACT was synthesized firstly from the reaction of 5-mercapto-1-methyltetrazole(MMT) and 7-ACA in C3-position of 7-ACA and then reacted with MAEM in C7-position to produce cefmenoxime(the yield was 86%),was proved to be superior to the route that the C7-position of 7-ACA was transformed before the C3-position(the yield was 69%).It was found that solvent has remarkable effect on the yield and dichloromethane can give the best result.Moreover,it was proved that ultrasound can significantly shorten the reaction time.

【关键词】 头孢甲肟盐酸头孢甲肟7-ACA超声
【Key words】 cefmenoximecefmenoxime hydrochloride7-ACAultrasound
【基金】 河北省自然科学基金资助项目(B2007000156)~~
  • 【分类号】R914
  • 【被引频次】4
  • 【下载频次】629
节点文献中: 

本文链接的文献网络图示:

本文的引文网络