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Synthesis and Antiinflammatory Activity of N-Aryl Anthranilic Acid and its Derivatives

机译:N-芳基邻氨基苯甲酸及其衍生物的合成及抗炎活性

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N-aryl anthranilic acid and its derivatives (3a-f) have been synthesized via Ullmann condensation of o-chloro benzoic acid with various substituted anilines (2a-f) in the presence of cupric oxide and anhydrous potassium carbonate. All the synthesized compounds (3a-f) were characterized by mp, TLC, UV, IR, H NMR and mass spectral analysis. All the synthesized compounds (3a-f) were screened for their antiinflammatory activity by carrageenan induced rat paw edema method. All the synthesized compounds (3a-f) showed significant antiinflammatory activity. Compounds 3a and 3c were found to be the most potent compounds.
机译:N-芳基邻氨基苯甲酸及其衍生物(3a-f)是在氧化铜和无水碳酸钾存在下,通过邻氯苯甲酸与各种取代的苯胺(2a-f)的乌尔曼缩合反应合成的。通过mp,TLC,UV,IR,1 H NMR和质谱分析对所有合成的化合物(3a-f)进行表征。通过角叉菜胶诱导的大鼠爪水肿方法筛选所有合成的化合物(3a-f)的抗炎活性。所有合成的化合物(3a-f)均显示出显着的抗炎活性。发现化合物3a和3c是最有效的化合物。

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