首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Synthesis, Antibacterial and Lipoxygenase Activities of N-[(Dimethyl substituted)phenyl]-N-(4-chlorophenyl)-4-chlorobenzenesulfonainides
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Synthesis, Antibacterial and Lipoxygenase Activities of N-[(Dimethyl substituted)phenyl]-N-(4-chlorophenyl)-4-chlorobenzenesulfonainides

机译:N - [(二甲基取代)苯基] -N-(4-氯苯基)-4-氯苯磺酰胺的合成,抗菌和脂氧合酶活性

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摘要

In present research work, a new series of N-[(dimethyl subsdtuted)phenyl]-N-(4-chiorophenyl)-4-chlorobenzeiiesulfonainides (5a-f) was synthesized and also evaluated for their biological activities. The reaction of 4-chlorobenzenesulfonyl chloride (1) with dimethyl substituted aniline (2a-f) in aqueous alkaline medium yielded N-[(dimethyl substituted)phenyl]-4-chlorobenzenesulfonamides (3a-f). The target compounds 5a-f were synthesized by reacting the compounds 3a-f with electrophile, 4-chlorobenzyl chloride (4) in aprotic solvent, DMF and NaH. All the synthesized compounds were characterized by IR, ~1HNMR and EIMS. All the synthesized derivatives were screened for antibacterial potential and were also subjected for lipoxygenase enzyme inhibition activity.
机译:在目前的研究工作中,合成了一种新的N - [(二甲基(二甲基)苯基] -N-(4-氯苯基)-4-氯苯并异嘧啶(5A-F),并评估其生物活性。 4-氯苯磺酰氯(1)与二甲基取代的苯胺(2A-F)在水性碱培养基中的反应得到N - [(二甲基取代)苯基] -4-氯苯磺酰胺(3A-F)。 通过使化合物3A-F与电子泳溶剂,DMF和NaH中的化合物,4-氯苯氯(4)反应来合成目标化合物5A-F。 所有合成的化合物的特征在于IR,〜1HNMR和EIMS。 筛选所有合成的衍生物用于抗菌潜力,也进行脂氧酶酶抑制活性。

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