合成具有抗炎活性的新型N-(3-氯-4-氟苯基)-2-(5-(3-(4-羟基- 2,2 -二甲基- 2,3 -二氢苯并呋喃-5-基)-1-苯基- 1h -吡唑-4-基)亚甲基)-4-氧-2-硫氧噻唑烷-3-基)乙酰胺

K. Shyam Sunder , Jayapal Maleraju
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引用次数: 8

摘要

通过1位和3位取代的吡唑(苯基和苯并呋喃)与不同取代的N-(3-氯-4-氟苯基)-2-(4-(3-(4-羟基- 2,2 -二甲基-2,3-二氢苯并呋喃-5-基)-1-苯基- 1h -吡唑-4-基)乙酰胺反应,合成了8个N-(3-氯-4-氟苯基)-2-(4-氧-2-硫氧噻唑-3-基)乙酰胺衍生物。这一系列反应如下图所示。这些化合物的化学结构通过1H NMR、IR和质谱进行了确证。测定化合物的抗炎活性。其中化合物10a、10b和10d具有显著的抗炎活性,10c具有中等的抗炎活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Synthesis of novel N-(3-chloro-4-flurophenyl)-2-(5-((3-(4-hydroxy-2, 2-dimethyl-2, 3-dihydrobenzofuran-5-yl)-1-phenyl-1H-pyrazol-4-yl) methylene)-4-oxo-2-thioxothiazolidin-3-yl) acetamides having anti-inflammatory activity

Eight derivatives of N-(3-chloro-4-fluorophenyl)-2-(5-((3-(4-hydroxy-2, 2-dimethyl l-2,3-dihydrobenzofuran-5-yl)-1-phenyl-1H-pyrazol-4-yl)methylene)-4-oxo-2-thioxothiazolidin-3-yl) acetamide were synthesized by reacting pyrazole having substitutions at 1 and 3 positions (phenyl and benzofuran) with various substituted N-(3-chloro-4-fluorophenyl)-2-(4-oxo-2-thioxothiazolidin-3-yl)acetamides.The series of reactions are depicted in following scheme. The chemical structures of these compounds were confirmed by means of 1H NMR, IR and Mass spectra. The compounds were assayed for anti-inflammatory activity.

Among the compounds 10a, 10b and 10d showed significant anti-inflammatory activity, 10c showed moderate anti-inflammatory activity.

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