头孢拉定合成工艺的优化  

Optimization of Cefradine Synthesis Process

作　　者：李文杰 曹桂僖 Li Wen-jie;Cao Gui-xi(Henan Kang Da Pharmaceutical Co.,Ltd.,Zhoukou 466200)

机构地区：[1]河南康达制药有限公司,周口466200

出　　处：《国外医药（抗生素分册）》2019年第1期65-68,共4页World Notes on Antibiotics

摘　　要：7-ADCA与四甲基胍反应形成胍盐,再与苯酐氨酸邓钠盐的混合酸酐缩合,经水解得到头孢拉定,收率>94%。此工艺优化了反应条件,找到了可行的检测方法来监控反应终点,省去了炭脱色步骤,采用抽除二氯甲烷的方法稳定晶型,还可以从母液中回收复盐并套用,易于工业化生产。The cefradine is synthesized by hydrolysis from the condensation products of guanidine salt, which is the combination of 7-Aminodesacetoxycephalosporanic acid with an overall yield of more than 94%. It is easy to realize industrial mass production by optimizing reaction conditions and finding a feasible detection method to monitor the ending point of the reactions. It is also feasible to take several other measures to realize industrial mass production, including eliminating carbon decoloring process, adopting the method of pumping methylene chloride to stablize crystal structure and recycling double salts to reuse.

关 键 词：7-ADCA 混合酸酐法 合成 头孢拉定 复盐 

分 类 号：R914[医药卫生—药物化学]