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左氧氟沙星绿色合成工艺 被引量:4

Green Synthesis of Levofloxacin
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摘要 介绍一种合成左氧氟沙星的新工艺。以(2,3,4,5)-四氟苯甲酰氯为起始原料,与3-乙氧基丙烯酸乙酯反应,然后L-氨基丙醇进行胺化反应,环合、水解后与N-甲基哌嗪缩合制得左氧氟沙星,总收率为50.15%。该工艺操作简单,环境污染小,符合绿色化学发展方向,值得进一步研究和推广。 New process for preparing Levofloxacin was described. The target was prepared from (2,3,4,5 )- fluorobenzoic chloride, which reacted with ethyl 3-ethoxyacrylate, amination with S-(+ )-2-aminopropanol, cyclization ,hydrolysis and condensation with N-methyl piperazine. The total yield was 50.15%. The process has many advantages, such as simple operation, less environmental pollution. In line with the green chemistry development direction, it deserves further research and popularization.
出处 《浙江化工》 CAS 2013年第9期13-15,22,共4页 Zhejiang Chemical Industry
关键词 左氧氟沙星 3-乙氧基丙烯酸乙酯 绿色合成 Levofloxacin ethyl 3-ethoxyacrylate green synthesis
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