首页> 外文期刊>Indian Journal of Heterocyclic Chemistry. (Text in English) >SYNTHESIS OF BENZOTHIAZOLE SUBSTITUTED 4-ARYLIDENE-5-METHYL-2,4-DIHYDRO-3H-PYRAZOL-3-ONES AND 3-METHYL-4,5-DIARYL-4,5-DIHYDROPYRAZOLO [3,4-c] PYRAZOLES AS ANTIMICROBIAL AGENTS
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SYNTHESIS OF BENZOTHIAZOLE SUBSTITUTED 4-ARYLIDENE-5-METHYL-2,4-DIHYDRO-3H-PYRAZOL-3-ONES AND 3-METHYL-4,5-DIARYL-4,5-DIHYDROPYRAZOLO [3,4-c] PYRAZOLES AS ANTIMICROBIAL AGENTS

机译:苯并噻唑取代4-芳基-5-甲基-2,4-二氢-3H-吡唑-3-酮和3-甲基-4,5-二芳基-4,5-二羟基吡唑并[3,4-c]吡唑的合成抗菌剂

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摘要

2-(1,3-Benzothiazol-2-yl)-4-arylidene-5-methyl-2,4-clihydro-3H-pyrazol-3-ones(3a-f) were synthesized by stirring a mixture of 2-(1,3-benzothiazol-2-yl)-5-methyl-2,4-dihydro-3H-p,yrazol-3-one (2) and suitably substituted araldehydes in basic medium. Further compounds 3b and 3c on cyclocondensation with phenyl hydrazine in the presence of few drops of gl acetic acid furnished the desired compounds 4a and 4b. The synthesized compounds were tested for their in vitro antimicrobial activity. Compound 3f showed maximum inhibitory activity against the tested Gram-positive bacteria Enterococcus faecalis whereas compounds 3b and 3c exhibited significant activity against Candida albicans.
机译:通过搅拌2-(1,3-二甲基苯并(2-,1,3-苯并噻唑-2-基)-4-亚芳基-5-甲基-2,4-clihydro-3H-吡唑-3-酮(3a-f)。在碱性介质中的1,3-苯并噻唑-2-基)-5-甲基-2,4-二氢-3H-p,吡唑-3-酮(2)和适当取代的芳醛。在几滴1g乙酸存在下与苯肼环缩合的其他化合物3b和3c提供了所需的化合物4a和4b。测试合成的化合物的体外抗菌活性。化合物3f对测试的革兰氏阳性细菌粪肠球菌显示出最大的抑制活性,而化合物3b和3c对白色念珠菌显示出显着的活性。

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