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班布特罗的合成[J]. 中国药科大学学报, 1999, (4): 11-12.
引用本文: 班布特罗的合成[J]. 中国药科大学学报, 1999, (4): 11-12.
The Synthesis of Ba m buterol[J]. Journal of China Pharmaceutical University, 1999, (4): 11-12.
Citation: The Synthesis of Ba m buterol[J]. Journal of China Pharmaceutical University, 1999, (4): 11-12.

班布特罗的合成

The Synthesis of Ba m buterol

  • 摘要: 班布特罗作为支气管解痉药具有作用时效长,副作用特别是对心血管系统的副作用非常微弱等优点。作者对文献合成方法进行了合理的改进,避免使用苄基保护的特丁胺和加压氢化还原脱苄基,简化了实验步骤和原材料,反应总收率比文献收率提高了1 .5 倍,达到56 % ,较大地降低了生产成本。

     

    Abstract: Bambuterol ,as a bronchodilator ,exhibits the prolonged duration of bronchospasmolytic activity and verylow side effects especially to heart blood vessal system . The synthetic method of bambuterol was improved , inimproved method the compound of t bu

     

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