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首页> 外文期刊>ACS Omega >Facile Synthesis and Antimicrobial Activities of Novel 1,4-Bis(3,5-dialkyl-4H-1,2,4-triazol-4-yl)benzene and 5-Aryltriaz-1-en-1-yl-1-phenyl-1H-pyrazole-4-carbonitrile Derivatives
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Facile Synthesis and Antimicrobial Activities of Novel 1,4-Bis(3,5-dialkyl-4H-1,2,4-triazol-4-yl)benzene and 5-Aryltriaz-1-en-1-yl-1-phenyl-1H-pyrazole-4-carbonitrile Derivatives

机译:新型1,4-BIS(3,5-二烷基-4H-1,2,4-三唑-4-基)苯和5-芳基三Z-1-ZEN-1-YL-1-苯基的容易合成和抗微生物活性-1H-吡唑-4-碳腈衍生物

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A group of novel 1,4-bis(3,5-dialkyl-4H -1,2,4-triazol-4-yl)benzene and 5-aryltriaz-1-en-1-yl-1-phenyl-1H -pyrazole-4-carbonitrile derivatives have been successfully synthesized and characterized by spectroscopic analyses. The triazenes were obtained in moderate yield by a coupling reaction between 5-aminopyrazol-4-carbonitrile and aryl diazonium chlorides, and their structures were confirmed by detecting the CN functional group in both IR and ~(13)C NMR spectra. Conversely, the novel 1,4-bis(3,5-dialkyl-4H -1,2,4-triazol-4-yl)benzene derivatives were obtained using a previously unreported and facile pathway starting with p -phenylenediamine with selected triethyl orthoalkylates and then hydrazine monohydrate, followed by refluxing in triethyl orthoalkylates. The structure of the methyl derivative was confirmed by X-ray analysis. The synthesized compounds were tested and evaluated as antimicrobial agents.
机译:一组新型1,4-BIS(3,5-二烷基-4℃H-1,2,4-三唑-4-基)苯和5-芳基三Z-1-EN-1-YL-1-通过光谱分析成功地合成并表征了苯基-1-4-碳腈衍生物。通过在5-氨基吡唑-4-腈和芳基重氮氧化芳族酰氯之间的偶联反应中适度地获得三聚旋,通过检测IR和〜(13)C NMR光谱中的CN官能团来证实它们的结构。相反,使用以前未报告的和容易的途径获得新的1,4-BIS(3,5-二烷基-4℃-1,2,4-三唑-4-基)苯衍生物,从而从开始对苯二胺与选自三乙基邻乙酯然后肼一水合物,然后在三乙基邻烷基化物中回流。通过X射线分析证实了甲基衍生物的结构。通过合成的化合物进行测试并评价为抗微生物剂。

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