首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >One-Pot Synthesis of N-Alkyl Purine, Pyrimidine and Azole Derivatives fron Alcohols using Ph_3P/CCl_4: A Rapid Route to Carboacyclic Nucleoside Synthesis
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One-Pot Synthesis of N-Alkyl Purine, Pyrimidine and Azole Derivatives fron Alcohols using Ph_3P/CCl_4: A Rapid Route to Carboacyclic Nucleoside Synthesis

机译:使用Ph_3P / CCl_4一锅法合成N-烷基嘌呤,嘧啶和唑衍生物的醇:快速合成碳环核苷的途径

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摘要

A facile and efficient method for one-pot N-alkylation of nucleobases and azole derivatives from alcohols using triphe-nylphosphine in carbon tetrachloride is described. In this method, treatment of alcohols with a mixture of triphenylphosphine, carbon tetrachloride, nucleobase or azole derivatives and potassium carbonate in the presence of catalytic amounts of tetra-n-butylammo-nium iodide (TBAI) in refluxing N,N-dimethylformamide, furnishes the corresponding N-alkyl derivatives in good yields. This methodology is highly efficient for various structurally diverse primary alcohols and also useful for N-alkylation of other N-heterocy-cles containing an acidic N-H bond.
机译:描述了一种在三氯化碳中使用三苯甲基膦对醇的核碱基和唑衍生物进行一锅N-烷基化的简便有效方法。在这种方法中,在催化量的四正丁基碘化碘化铵(TBAI)存在下,在回流的N,N-二甲基甲酰胺中,用三苯基膦,四氯化碳,核碱基或唑衍生物和碳酸钾的混合物处理醇,得到了相应的N-烷基衍生物,收率很高。该方法学对于各种结构多样的伯醇是高效的,并且也可用于含有酸性N-H键的其他N-杂环的N-烷基化。

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