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盐酸米多君的合成 被引量:2

Synthesis of Midodrine Hydrochloride
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摘要 以对苯二酚为原料 ,经酯化、重排、醚化、溴代、胺化、酰胺化、叠氮化、硼氢化钾 /钯炭还原等 8步反应合成盐酸米多君。还原反应改用成本较低的硼氢化钾 ,操作简单 ,条件温和。总收率 15 .1%。 Midodrine Hydrochloride was synthesized from hydroquinone by esterification, rearrangement, etherification, bromination, amination, amidation, azidation and reduction with an overall yield of 15.1%.
出处 《中国医药工业杂志》 CAS CSCD 北大核心 2002年第5期213-215,共3页 Chinese Journal of Pharmaceuticals
关键词 盐酸米多君 α-受体激动剂 升压药 合成 midodrine hydrochloride α adrenergic stimulating agent raising blood pressure synthesis
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参考文献6

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同被引文献3

  • 1Ray AK,Patel H,Patel MR.Synthesis of midodrine hydrochloride by the reduction of the novel intermediate 1-(2′,5′-dimethoxyphenyl) -2-azidoethanone[P].US:6201153,2001-03-13.(CA 2001,134:208133)
  • 2Epifani E,Lapucci A,Macchia B,et al.Conformational effects on the activity of drugs.10.Synthesis,conformation,and pharmacological properties of 1-(2,5-dimethoxyphenyl) -2-aminoethanols and their morpholine analogs[J].J Med Chem,1983,26(2):254-259.
  • 3孙逊,陈纪岳,董纪昌.甲砜霉素氯乙酸酯Delepine反应的研究[J].中国药学杂志,1999,34(7):493-495. 被引量:1

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