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伊潘立酮合成缩合反应的工艺改进
引用本文:李陈.伊潘立酮合成缩合反应的工艺改进[J].辽宁化工,2011(8):783-784.
作者姓名:李陈
作者单位:四川阳光润禾药业;
摘    要:通过对伊潘立酮关键缩合反应的工艺条件优化,最终确定的最佳反应工艺为:以6-氟-3-(4-哌啶基)-1,2-苯并异噁唑盐酸盐和1-4-(3-氯丙氧基)-3-甲氧苯基]乙酰酮为原料,乙腈为溶媒,碳酸钾为束酸剂,于74~81℃缩合成伊潘立酮;收率86.4%

关 键 词:伊潘立酮  合成  工艺优化

Improvement of Condensation Process for Synthesizing Iloperidone
LI Chen.Improvement of Condensation Process for Synthesizing Iloperidone[J].Liaoning Chemical Industry,2011(8):783-784.
Authors:LI Chen
Affiliation:LI Chen(Sichuan Sunheal Pharmaceutical Company Limited,Sichuan Chengdu 610041,China)
Abstract:By the technological optimization of condensation process for synthesizing Iloperidone,the optimum technology conditions were determined as follows: 6-Fluoro-3-(4-piperidine)-1,2-benzoisoxazole hydrochloride and 1-4-(3-chloropropoxy)-3-methoxyphenyl]ethanone were used as starting material,acetonitrile was used as solvent,potassium carbonate was used as acid trapping agent,the condensation reaction was carried out at 74~81 ℃,yield of product was 86.4%.
Keywords:Iloperidone  Synthesis  Process optimization  
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