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萘哌地尔合成工艺的改进
引用本文:汪洪湖,谢延,蔡奇峰.萘哌地尔合成工艺的改进[J].安徽化工,2011,37(3):23-25.
作者姓名:汪洪湖  谢延  蔡奇峰
作者单位:蚌埠丰原涂山制药有限公司,安徽蚌埠,233010;蚌埠丰原涂山制药有限公司,安徽蚌埠,233010;蚌埠丰原涂山制药有限公司,安徽蚌埠,233010
摘    要:改进了萘哌地尔的合成工艺条件:投料比n(3-(1-萘氧基)-1,2-环氧丙烷)∶n(邻甲氧基哌嗪氢溴酸盐)∶n(K2CO3)=1.01∶1∶1.5,以氯仿-水的非均相溶液为反应溶剂,在回流温度(60~63℃)反应5h制得萘哌地尔粗品;再以丙酮-水(4∶1)为溶剂,精制得到高纯度的成品(纯度≥99%)。该工艺条件温和,操作简便,产品质量稳定可靠,两步总收率达到72.3%。

关 键 词:萘哌地尔  合成工艺  精制

Improved Synthesis of Eapidil
WANG Hong-hu,XIE Yan,CAI Qi-feng.Improved Synthesis of Eapidil[J].Anhui Chemical Industry,2011,37(3):23-25.
Authors:WANG Hong-hu  XIE Yan  CAI Qi-feng
Affiliation:WANG Hong-hu,XIE Yan,CAI Qi-feng(Bengbu BBCA Tushan Medicine Co.,Ltd.,Bengbu 233010,China)
Abstract:This article introduced the process conditions of improved synthetic process for Eapidil:the mole ratio was 3-(1-naphthyloxy)-1,2-propylene oxide∶o-methoxypiperazine∶Potassium carbonate=1.01 ∶ 1.0 ∶ 1.5,solvent:mixture of chloroform and water,reaction temperature:60~63℃,and reaction time:5h.Refine the final product via the mixture solvent of acetone and water(4 ∶ 1).The purity of Eapidil was not less than 99% with 72.3% overall yield.This process conditions were not severe and has simplified operation and high quality product.
Keywords:Eapidil  synthetic process  refine  
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