首页> 外文期刊>Journal of chemical research: reviews and research papers from all branches of chemistry >Synthesis, crystal structures and xanthine oxidase inhibitory activity of 2-(benzylthio)-5-[1-(4-fluorobenzyl)-3-phenyl-1H-pyrazol-5-yl]-1,3,4-oxadiazoles derivatives
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Synthesis, crystal structures and xanthine oxidase inhibitory activity of 2-(benzylthio)-5-[1-(4-fluorobenzyl)-3-phenyl-1H-pyrazol-5-yl]-1,3,4-oxadiazoles derivatives

机译:2-(苄硫基)-5- [1-(4-氟苄基)-3-苯基-1H-吡唑-5-基] -1,3,4-恶二唑衍生物的合成,晶体结构和黄嘌呤氧化酶抑制活性

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摘要

A synthetic route for the preparation of 2-(benzylthio)-5-[1-(4-fluorobenzyl)-3-phenyl-1H-pyrazol-5-yl]-1,3,4-oxadiazoles derivatives from ethyl 3-phenyl-1H-pyrazole-5-carboxylate has been developed. The configurations of the intermediate 1,3,4-oxadiazole-2-thione and 3-bromobenzylthio substituted 1,3,4-oxadiazole were determined by single crystal X-ray diffraction analysis. The in vitro xanthine oxidase inhibitory activity of these compounds was evaluated.
机译:由乙基3-苯基制备2-(苄硫基)-5- [1-(4-氟苄基)-3-苯基-1H-吡唑-5-基] -1,3,4-恶二唑衍生物的合成路线已经开发了-1H-吡唑-5-羧酸酯。通过单晶X射线衍射分析确定中间体1,3,4-恶二唑-2-硫酮和3-溴苄硫基取代的1,3,4-恶二唑的构型。评价了这些化合物的体外黄嘌呤氧化酶抑制活性。

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