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首页> 外文期刊>Der Pharma Chemica: journal for medicinal chemistry, pharmaceutical chemistry and computational chemistry >A Novel One Pot Facile Synthesis of 1,2,4-Triazolo-1,3,4-Thiadiazepino Fused Coumarins and Their Antimicrobial and Antituberculosis Activity Studies
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A Novel One Pot Facile Synthesis of 1,2,4-Triazolo-1,3,4-Thiadiazepino Fused Coumarins and Their Antimicrobial and Antituberculosis Activity Studies

机译:新型一锅法合成1,2,4-三唑-1,3,4-硫二氮杂吡啶香豆素及其抗菌和抗结核活性的研究

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摘要

A novel series of [1,2,4]triazolo[3’,4’:2,3][1,3,4]thiadiazepino[7,6-b]coumarins (3a-l) was synthesized by the reaction of appropriate 4-chloro 3-formyl coumarins (1a-c) with various 4-amino-5-substituted-3-mercapto-1,2,4-triazoles (2a-d) in ethanol in the presence of a catalytic amount of K2CO3 under refluxing conditions. The structures of the synthesized compounds were established by elemental analysis and spectral data like IR, 1H-NMR, 13C-APT and mass analysis. The synthesized compounds were screened for their antimicrobial and antituberculosis activity. Among all the synthesized compounds, the compounds 3a, 3e, 3j and 3k were found to be more active against tested pathogens.
机译:通过(1a-1)的反应合成了一系列新的[1,2,4]三唑[3',4':2,3] [1,3,4]噻二氮杂[7,6-b]香豆素(3a-1)。在催化量的K2CO3存在下,在乙醇中添加适当的4-氯3-甲酰基香豆素(1a-c)与各种4-氨基-5-取代的-3-巯基-1,2,4-三唑(2a-d)在回流条件下。通过元素分析和光谱数据(例如IR,1H-NMR,13C-APT和质量分析)建立了合成化合物的结构。筛选合成的化合物的抗微生物和抗结核活性。在所有合成的化合物中,发现化合物3a,3e,3j和3k对测试的病原体更具活性。

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