摘要
目的合成盐酸帕罗西汀。方法以(-)-trans-4-(4-氟苯基)-3-羟甲基-1-甲基哌啶为原料经酯化、醚化、水解3步反应合成(-)-盐酸帕罗西汀。结果合成了盐酸帕罗西汀,总收率71.0%。结论本方法可以方便地合成盐酸帕罗西汀,操作简便,提高了收率,缩短了反应时间。
出处
《中国医药指南》
2011年第19期233-234,共2页
Guide of China Medicine
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引证文献5
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二级引证文献4
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