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Click Synthesis of Some mono/bis 1,2,3-Triazoles with Ester Linkage and their Microbicidal Activity

机译:用酯连杆和它们的微生物活性单击一些单声道/双1,2,3-三唑的合成

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摘要

Synthesis of some new 1,4-disubstituted 1,2,3-triazoles with ester functionality is reported employing Cu(I) catalyzed Huisgen [3+2] cycloaddition reaction of prop-2-yn-1-yl benzoates with 1,4-phenylenebis(methylene) bis(2-azidoacetate) and benzyl 2-azidoaeetates. The synthesized compounds were well characterized through FTIR, ~1H NMR, ~(13)C NMR and HRMS. Further, the synthesized triazole derivatives were accessed for in vitro antimicrobial activity against one Gram-positive bacterial strain Staphylococcus aureus, three Gram-negative bacterial strains Escherichia coli, Klebsiella pneumoniae, Enterobacter aerogenes and two fungi Candida albicans and Aspergillus niger. Few of the synthesized disubstituted 1,2,3-triazoles displayed moderate to good inhibitory activity against tested microbial strains.
机译:将一些新的1,4-二取代的1,2,3-三唑与酯官能团的合成催化的HUISGEN [3 + 2]环加成反应的催化剂官能团用1,4 - 白基比斯(亚甲基)双(2-氮杂乙酸酯)和苄基2-氮杂化酸盐。 合成化合物通过FTIR,〜1H NMR,〜(13)C NMR和HRMS表征得很好。 此外,对合成的三唑衍生物用于对一个革兰氏阳性细菌菌株金黄色葡萄球菌的体外抗微生物活性,三克阴性细菌菌株大肠杆菌,Klebsiella肺炎,肠杆菌空气和两种真菌念珠菌和曲霉。 少量合成二二烯化的1,2,3-三唑显示出对测试的微生物菌株的良好抑制活性。

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