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首页> 外文期刊>Oriental Journal of Chemistry: An International Research Journal of Pure & Applied Chemistry >Synthesis, Antimicrobial and Antitubercular Activities of Some Novel Carboxamide Derivatives of 2-quinolones
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Synthesis, Antimicrobial and Antitubercular Activities of Some Novel Carboxamide Derivatives of 2-quinolones

机译:几种新颖的2-喹诺酮羧酰胺衍生物的合成,抗菌和抗结核活性

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摘要

A series of novel substituted N-(3-acetyl-2-oxoquinolin-1(2H)-yl)benzamide (AJQC1-AJQC12) have been synthesized upon refluxing 3-acetyl-1-amino-quinolin-2-one and substituted benzoic acid in the presence of dry redistilled pyridine and silicon tetrachloride as coupling agent. 3-acetyl-1-amino-quinolin-2-one (AJQ1-AJQ12) were synthesized from substituted 3-acetyl coumarin upon refluxing with hydrazine hydrate and ethanol.The structures of the final carboxamide derivatives were confirmed by IR, ~1H NMR and mass spectra. The synthesized compounds were screened for their antimicrobial activity by tube dilution method and antitubercular activity by microplate Alamar blue assay. Most of the compounds have exhibited promising antibacterial, antifungal and antitubercular activities.
机译:通过回流3-乙酰基-1-氨基-喹啉-2-酮和取代苯甲酸合成了一系列新颖的取代N-(3-乙酰基-2-氧喹啉-1(2H)-基)苯甲酰胺(AJQC1-AJQC12)在干燥的重蒸吡啶和四氯化硅为偶合剂的条件下,加入酸。在水合肼和乙醇回流下,由取代的3-乙酰基香豆素合成3-乙酰基-1-氨基-喹啉-2-酮(AJQ1-AJQ12),并通过IR,〜1H NMR和IR确定了最终甲酰胺衍生物的结构。质谱。通过试管稀释法筛选合成的化合物的抗微生物活性,并通过微板Alamar蓝测定法筛选合成的化合物的抗结核活性。大多数化合物已显示出令人鼓舞的抗菌,抗真菌和抗结核活性。

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