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首页> 外文期刊>Asian journal of research in chemistry >Microwave assisted synthesis and antifungal studies of 5-amino thiadiazole substituted pyrimidine compounds
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Microwave assisted synthesis and antifungal studies of 5-amino thiadiazole substituted pyrimidine compounds

机译:微波辅助合成和5-氨基噻二唑取代嘧啶化合物的抗真菌研究

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Simple synthetic methods of 5-(5-amino-1,3,4-thiadiazol-2yl)-3,4-dihydro-6-methyl-4-phenylpyrimidin-2(1H)-thione (3f-j) are described. Compound 1 is converted to carbothiamide 2 by reacting compound 1 with thiosemicarbazide in catalytic amount of acetone is irradiated with help of domestic microwave oven (200W) for 2 minutes. Compound 2 is act as a key intermediate for the final compounds. The compound 2 is converted to corresponding thiadiazole 3 by treatment with conc.H2SO4 and NH3 Structural elucidation is accomplished by IR, ~1H and ~(13)CNMR, Elemental analysis and GC-Mass spectral data of the synthesized compounds. Few of these Pyrimidine derivatives have been evaluated for their possible antifungal activity. Most of the tested compounds show significant antifungal activity.
机译:描述了5-(5-氨基-1,3,4-噻二唑-200L)-3,4-二氢-6-甲基-4-苯基吡啶胺-2(1H)的简单合成方法。 通过使化合物1在催化量的丙酮中用硫代氧化物反应转化为碳金属2,用国内微波炉(200w)的催化量丙酮2分钟照射。 化合物2作为最终化合物的关键中间体。 通过用CONC 3 2 SO 4处理,将化合物2转化为相应的噻二唑3,NH 3结构阐明通过IR,〜1H和〜(13)CNMR,元素分析和合成化合物的GC质谱数据。 已经评估了这些嘧啶衍生物中的少数用于其可能的抗真菌活性。 大多数测试化合物显示出显着的抗真菌活性。

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