3──~(14)C靛玉红的合成

  • 摘要: 用K ̄(14)CN制取N,N′-二苯基 ̄(14)C氰甲脒,将脒环化、水解为3── ̄(14)C吲哚醌,再使吲哚醌与吲哚酚钾缩合即得3- ̄(14)C靛玉红。此合成方法步骤简单、操作方便;所得产品比活度为2GBq/mmol,放射化学纯度>99.9%。

     

    Abstract: THE SYNTHESIS IF 3-~(14)CINDIRUBIN Gu Meiying;Zhang Xiuwen;Tian Shuhao(Institute of Radiomedicine,Chinese Academy of Medical Sciences,Tianjin 300192)ABSTRACT 3-~(14)Cindirubin is synthesized in three steps from potassium ~(14)Ccyanide. First,Potassium~(14)Ccyanide reacts with N,N′-diphenyltbiourea to get N,N′-diphenyl~(14)Ccyanoamidine,Then.cyclizated in the presence of anhydrous aluminium chloride and hydrolizated with hydrochloric acid,amidine is leaded to3-~(14)Cisatin,Finally,3-~(14)Cisatin is condensed with excess potassium 3-indole-late to yield3-~(14)Cindirubin in 20. 34%overall radiochemical yield from K~(14)CN with a specific activi-ty of 2 GBq/mmol and a radiochemical purity of 99.9%(TLC).Key words potassium~(14)Ccyanide3-~(14)Cindirubin synthesis

     

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