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Continuous preparation for rifampicin
Journal of Flow Chemistry ( IF 2.7 ) Pub Date : 2018-11-23 , DOI: 10.1007/s41981-018-0017-2 Xin Li , Zhuang Liu , Hao Qi , Zheng Fang , Siyu Huang , Shanshan Miao , Kai Guo
中文翻译:
连续制备利福平
更新日期:2018-11-23
Journal of Flow Chemistry ( IF 2.7 ) Pub Date : 2018-11-23 , DOI: 10.1007/s41981-018-0017-2 Xin Li , Zhuang Liu , Hao Qi , Zheng Fang , Siyu Huang , Shanshan Miao , Kai Guo
To reduce the cost and improve the efficiency for rifampicin preparation, a continuous flow synthesis of rifampicin starting from rifamycin S and tert-butylamine was studied in a microreactor. Two reaction steps and one purification step were coupled in a microreactor, and rifampicin was obtained with 67% overall yield. This method used 25% less 1-amino-4-methyl piperazine and got 16% higher overall yield without changing solvent and purification process between steps. This method has a good potential for further industrial application.
中文翻译:
连续制备利福平
为了降低成本并提高利福平的制备效率,在微反应器中研究了以利福霉素S和叔丁胺为起始原料连续流动合成利福平的方法。将两个反应步骤和一个纯化步骤在微反应器中偶联,获得利福平,总产率为67%。此方法使用的1-氨基-4-甲基哌嗪减少了25%,总产率提高了16%,而无需在步骤之间更改溶剂和纯化工艺。该方法具有进一步工业应用的良好潜力。