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首页> 外文期刊>Journal of the Chilean Chemical Society >A CONVENIENT SYNTHESIS AND CYTOTOXIC ACTIVITY OF 3-ARYL-5-PENTYL-1,2,4-OXADIAZOLES FROM CARBOXYLIC ACID ESTERS AND ARYLAMIDOXIMES UNDER SOLVENT-FREE CONDITIONS
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A CONVENIENT SYNTHESIS AND CYTOTOXIC ACTIVITY OF 3-ARYL-5-PENTYL-1,2,4-OXADIAZOLES FROM CARBOXYLIC ACID ESTERS AND ARYLAMIDOXIMES UNDER SOLVENT-FREE CONDITIONS

机译:无溶剂条件下来自羧酸酯和芳基酰胺的3-ARYL-5-PENTYL-1,2,4-恶二唑的简便合成和细胞毒活性

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摘要

The synthesis of 3-aryl-5-pentyl-1,2,4-oxadiazoles from carboxylic acid esters and arylamidoximes in the presence of potassium carbonate is described. The reaction was carried out in a microwave oven without any solvent in much shorter time and in good yields. The structures of the synthesized compounds were elucidated using IR, 1H and 13C NMR spectroscopy and elemental analysis and their antiproliferative activities was evaluated against three different human cell lines.
机译:描述了在碳酸钾存在下由羧酸酯和芳基酰胺肟合成3-芳基-5-戊基-1,2,4-恶二唑。该反应在没有任何溶剂的微波炉中进行,时间短得多,产率高。使用IR,1H和13C NMR光谱和元素分析阐明了合成化合物的结构,并针对三种不同的人类细胞系评估了它们的抗增殖活性。

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