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头孢噻呋的合成改进
赵增任
0
(国家兽药工程技术研究中心)
摘要:
对硫代呋喃甲酸进行精制,用乙酸乙酯作溶剂,与7-ACA反应得到头孢呋酸(收率95.6%,含量≥98.0% (HPLC归一化法)),在三乙胺作用下直接与AE-活性酯缩合得到头孢噻呋(收率:74.2%,含量≥95.0% (HPLC外标法)),产品可直接制备冻干粉。
关键词:  头孢呋酸  精制  缩合  头孢噻呋
DOI:
投稿时间:2011-07-07修订日期:2011-08-03
基金项目:
Modification of Synthetic Method of Ceftiofur
Zhao zengren
(guojiashouyaogongchengjishuyanjiuzhongxin)
Abstract:
Purified 3-Thiofuroyi-formic acid reacts with 7- ACA to get 3-Thiofuroyi -7-Aminocephalosporanic acid using ethyl acetate as solvent (yield :95.6% , ), highly pure product(≥ 98.0%,HPLC).under the action of triethylamine, 3-Thiofuroyi-7- Aminocephalosporanic acid reacts with AE-thiolester to get ceftiofur (yield: 74.2%), highly pure product(≥ 95.0%,HPLC) , which can be prepared for freeze-dried powder directly .
Key words:  3-thiofuroyi-7-aminocephalosporanic acid  purification  7-ACA  ceftiofur

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