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Synthesis of pyrazolines and cyanopyridines as potnetial antimicrobial agents

机译:吡唑啉和氰基吡啶类化合物作为潜在的抗菌剂的合成

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摘要

3,3'-Bis(4-acetophenylaminosulphonyl)benzophenone 1 on condensation with various aldehydes yields chalcones 2a-p which on cyclization with hydrazine hydrate and malononitrile furnishes the corresponding 3,3'-bis(5-aryl-1H/acetyl-pyrazolin-3-yl-4-phenylaminosulphonyl)benzophenones 3a-p,3'a-p and 3,3'-bis(2-amino-3-cyano-4-aryl pyridin-6-yl-4-phenylaminosulphonyl)benzophenones 4a-p.THe structure of the compounds have been confirmed from elemental analyses,IR,~1H NMR and mass spectral data.All the products have been evaluated for their in vitro growht inhibitory activity against different microbes.
机译:与各种醛缩合的3,3'-双(4-乙酰苯基氨基磺酰基)二苯甲酮1生成查耳酮2a-p,在与水合肼和丙二腈环化后提供相应的3,3'-双(5-芳基-1H /乙酰基吡唑啉) -3-基-4-苯基氨基磺酰基)二苯甲酮3a-p,3'ap和3,3'-双(2-氨基-3-氰基-4-芳基吡啶-6-基-4-苯基氨基磺酰基)二苯甲酮4a-p通过元素分析,IR,〜1H NMR和质谱数据确定了化合物的结构。已评估了所有产品的体外对不同微生物的抑制活性。

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