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氟伏沙明的合成工艺改进
引用本文:刘滔,盛荣,胡永洲. 氟伏沙明的合成工艺改进[J]. 浙江大学学报(医学版), 2003, 32(5): 441-442
作者姓名:刘滔  盛荣  胡永洲
作者单位:浙江大学药学院,浙江,杭州,310031
摘    要:
目的:改进氟伏沙明的合成方法。方法:以对三氟甲基苯甲腈为原料,经格氏反应和水解制成5-甲氧基-4’-三氟甲基苯基戊酮,再经肟化制成5-甲氧基-4'-三氟甲基-O-(2-胺乙基)戊酮肟,最后与马来酸成盐制得氟伏沙明。结果:合成产物总收率达36.1%,其结构经核磁共振谱确证。结论:此改进的合成路线是可行的。

关 键 词:氟伏沙明 化学合成
文章编号:1008-9292(2003)05-0441-02
修稿时间:2001-07-11

Improved method of fluvoxamine synthesis
LIU Tao,SHENG Rong,HU Yong-zhou. Improved method of fluvoxamine synthesis[J]. Journal of Zhejiang University. Medical sciences, 2003, 32(5): 441-442
Authors:LIU Tao  SHENG Rong  HU Yong-zhou
Affiliation:College of Pharmaceutical Sciences Zhejiang University, Hangzhou 310031 China.
Abstract:
Objective: To modify the synthetic method of fluvoxamine. Methods: Fluvoxamine was synthesized from 4-trifluoromethylbenzonitrile by the steps of Grignard reaction, hydrolysis and oximation. Results: The chemical structure of the synthesized product was confirmed by 1HNMR, and the total yield reached to 36.16%. Conclusion: The results indicate that the synthetic route is practical.
Keywords:Fluvoxamine/chem syn
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