节点文献
司氟沙星合成工艺研究
SYNTHESIS OF SPARFLOXACIN
【摘要】 司氟沙星由2,3,4,5-四氟苯甲酸经硝化、酰氯化、缩合、环合、还原、水解、酰化,再与顺式2,6-二甲基哌嗪缩合、水解而得,工艺简便,反应条件温和,可用于工业化生产。
【Abstract】 A facile preparation of sparfloxacin,starting from 2,3,4,5 tetrafluorobenzoic acid,via nitration,chlorination,condensation,cyclization,reduction,hydrolysis,acylation,piperazination,hydrolysis,etc,is described.The reactions of all steps were carried out in moderate conditions to be applicable to large scale preparation.
【关键词】 司氟沙星;
氟喹诺酮;
抗菌剂;
合成;
【Key words】 sparfloxacin; fluoroquinolone; antimicrobial agent; synthesis;
【Key words】 sparfloxacin; fluoroquinolone; antimicrobial agent; synthesis;
- 【文献出处】 中国医药工业杂志 ,CHINESE JOURNAL OF PHARMACEUTICALS , 编辑部邮箱 ,1997年04期
- 【分类号】TQ460.31
- 【被引频次】17
- 【下载频次】256