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头孢唑啉的合成路线
引用本文:邢俊德. 头孢唑啉的合成路线[J]. 山西化工, 2000, 20(2): 14-15
作者姓名:邢俊德
作者单位:华北制药集团太原有限责任公司 太原
摘    要:概述了头孢唑啉的主要合成路线。第一条路线,7-ACA(7-氨基头孢烷酸)和噻二唑、四氮唑乙酸反应;第二路线,GCLE先和噻二唑反应,然后脱去3位和7位的保护基团,最后和四氮唑乙酸缩合;第三路线,噻二唑和四氮唑乙酸先形成活性硫醇酯,再与7-ACA反应;第四条路线,以噻唑淋-丁啶酮为起始原料进行反应。

关 键 词:氨基头孢烷酸 头孢唑啉 合成 抗菌素

Summary about Synthetic Methods of Cefazolin
Xing Junde. Summary about Synthetic Methods of Cefazolin[J]. Shanxi Chemical Industry, 2000, 20(2): 14-15
Authors:Xing Junde
Abstract:This article summarizes main methods of synthesising cefazolin. There are four synthesising routes. First route, a beginning material is 7-ACA. 7-ACA reacts with 2-mercapto-5-methylthiadiazole and tetrazole-1-acetic acid. Now it is main method of productive cefazolin. Second route, a beginning material is GCLE. GCLE reacts with 2-mercapto-5-methylthiadiazole. The reactant take off protective groups which lie in 3-place and 7-place. Then the compound reacts with tetrazole-1-acetic acid. This route is newer and good. Third route, 2-mercapto-5-methylthiadiazole and tetrazole-1-acetic acid form active thiol ester. Then the ester reacts with 7-ACA. This method isn't used in produce,bnt it has high yield and less procedure. There is a good prospect. Fourth route,a beginning material is thiazoline-azetidinones. It is in a study stage.
Keywords:7-AC A  GCLE  cefazolin  synthesis
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