摘要
氟罗沙星由2,3,4-三氟硝基苯经还原、缩合环合、氟乙基化、螯合、上甲基哌嗪、水解、精制等七步反应制得。反应条件温和,副反应少,总收率达40%。
An improved synthesis of antibacterial agent fleroxacin,starting from 2,3,4-trifluoronitrobenzene via reduction,condensation-cyclization,fluoroethylation,chelation,piperazination,hydrolysis,etc,was described.The reactions of all steps were carried out under very mederate conditions with the overall yield of 40%.
出处
《中国药科大学学报》
CAS
CSCD
北大核心
1995年第6期321-323,共3页
Journal of China Pharmaceutical University
关键词
氟喹诺酮类
抗菌剂
氟罗沙星
合成工艺
Fleroxacin
Fluoroquinolone antimicrobial agent
Synthesis