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首页> 外文期刊>Current Chemistry Letters >Synthesis and characterization of 4-((5-bromo-1H-pyrazolo [3,4-b]pyridin-3-yl)amino)-N-(substituted)benzenesulfonamide as Antibacterial, and Antioxidant Candidates
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Synthesis and characterization of 4-((5-bromo-1H-pyrazolo [3,4-b]pyridin-3-yl)amino)-N-(substituted)benzenesulfonamide as Antibacterial, and Antioxidant Candidates

机译:4 - ((5-溴-1H-吡唑[3,4-B]吡啶-3-基)氨基) - (取代)苯磺胺酰胺作为抗菌和抗氧化剂候选的合成和表征

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摘要

A series of novel 5-Bromo-3-iodo-1H-pyrazolo[3,4-b]pyridine linked various sulfonamidederivatives 8a-8j poly functionalized were designed and synthesized in moderate to goodyield. A starting with iodination of 5-Bromo-1H-pyrazolo[3,4-b]pyridine 5 with iodineproduced intermediate 5-Bromo-3-iodo-1H-pyrazolo[3,4-b]pyridine 6 with the reaction ofvarious sulfonamide derivatives 7a-7j via copper catalyzed coupling reaction producedtargeted compounds8a-8j. The isolated compounds were accepted by spectral and elementalanalysis. The compounds 8a,8c,8d, and 8i were excellent active against Gram-positive andgram-negative bacterial strain compare to streptomycin standard drug. All synthesizedcompounds showed moderate to good antioxidant properties with used DPPH and Superoxideradical scavenging assay, Compounds 8c, 8g, and 8i exerted significant antioxidant scavengingactivity for the DPPH radical.
机译:一系列新的5-溴-3-Iodo-1H-吡唑[3,4-B]吡啶连接各种磺胺胺,在中等至Goodyield中设计和合成。用碘过量的中间体5-溴-3-Iodo-1H-吡唑[3,4-B]吡啶6的5-溴-1H-吡唑[3,4-B]吡啶5的碘化碘化碘化碘化碘化碘化衍生物的反应7A-7J通过铜催化的偶联反应产生的化合物8A-8J。通过光谱和元素立体分析接受分离的化合物。与链霉素标准药物相比,化合物8a,8c,8d和8i对革兰氏阳性和曲线阴性细菌菌株的优异有效。所有合成组成均显示良好至良好的抗氧化性能,具有二手DPPH和超氧化物清除测定,化合物8C,8G和8I施加了DPPH激活的显着抗氧化清除活性。

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