首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis of some novel 3-Alkyl/aryl-6-((1H-benzo[d][1,2,3]triazol-1-yl) methyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazoles
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Synthesis of some novel 3-Alkyl/aryl-6-((1H-benzo[d][1,2,3]triazol-1-yl) methyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazoles

机译:某些新型3-烷基/芳基-6-(((1H-苯并[d] [1,2,3]三唑-1-基)甲基])-[1,2,4]三唑[3,4-b]的合成] [1,3,4]噻二唑

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摘要

(Chemical Equation Presented) A series of 3-alkyl/aryl substituted-6-((1H- benzo[d][1,2,3]triazol-1-yl)methyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadizoles 4a-m are prepared by the condensation of 3-alkyl/aryl substituted-4-amino-5- mercapto-1,2,4-triazoles 2a-m with benzotriazole-1-yl acetic acid 3 through a single step reaction. The structures of all newly synthesized compounds are established on the basis of their IR, ~1H NMR, and elemental analyses data. Two selected compounds 4l and 4m are investigated for their analgesic and anti-inflammatory activities; they showed weak anti-inflammatory activity and no analgesic activity.
机译:(给出的化学方程)一系列3-烷基/芳基取代的6-((1H-苯并[d] [1,2,3]三唑-1-基)甲基)-[1,2,4]三唑[通过将3-烷基/芳基取代的4-氨基-5-巯基-1,2,4-三唑2a-m与苯并三唑缩合制备3,4-b] [1,3,4]噻二唑4a-m -1-基乙酸3通过一步反应。所有新合成化合物的结构均基于其IR,〜1H NMR和元素分析数据确定。研究了两种选定的化合物4l和4m的镇痛和抗炎活性;它们显示出较弱的抗炎活性,没有镇痛活性。

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