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氟胞嘧啶合成工艺的改进 被引量:4

IMPROVED METHOD FOR SYNTHESIS OF 5-FLUOROCYTOSINE (5-FC)
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摘要 氟胞嘧啶(1,5-Fluorocytosine,简称5-Fc)系一抗深部真菌的有效药物。 A modified method for preparing 5-Fluorocytosine, a systemic antifungal agent. was described. The amination of 2-methyoxy-4-chloro-5-fluoropyrimidine was performed under normal pressure instead of high pressure as reported in literature. The process of the hydrolysis of 2-methyoxy-4-amino-5-fluoropyrimidine was optimized. The overall yield of the method was increased to 72%.
出处 《中国药科大学学报》 CAS CSCD 北大核心 1989年第1期35-36,共2页 Journal of China Pharmaceutical University
关键词 氟胞嘧啶 合成工艺 抗真菌药 Systemic antifungal agent: Synthesis of 5-fluorocytosine
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参考文献2

  • 1李年平.5-氟胞嘧啶与5-氟脲嘧啶的分离[J]医药工业,1983(07).
  • 2李年平,莫安国.5-氟胞嘧啶的合成[J]医药工业,1982(08).

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  • 2吴正,卫敏,张法智,沈军,段雪.酒石酸插层水滑石层间距的可控性研究[J].北京化工大学学报(自然科学版),2004,31(4):74-77. 被引量:4
  • 3张娴,张慧,卫敏,D.G.Evans,段雪.草甘膦插层镁铝水滑石MgAl-LDH-gly的释放性能研究[J].高等学校化学学报,2004,25(10):1869-1874. 被引量:7
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