Al-Azmi Amal, Mahmoud Huda
Chemistry Department, Kuwait University, P.O. Box 5969, Safat, Kuwait City 13060, Kuwait.
Department of Biological Sciences, Kuwait University, Kuwait City 13060, Kuwait.
ACS Omega. 2020 Apr 23;5(17):10160-10166. doi: 10.1021/acsomega.0c01001. eCollection 2020 May 5.
A group of novel 1,4-bis(3,5-dialkyl-4-1,2,4-triazol-4-yl)benzene and 5-aryltriaz-1-en-1-yl-1-phenyl-1-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 C NMR spectra. Conversely, the novel 1,4-bis(3,5-dialkyl-4-1,2,4-triazol-4-yl)benzene derivatives were obtained using a previously unreported and facile pathway starting with -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.
通过光谱分析成功合成并表征了一组新型的1,4-双(3,5-二烷基-4-1,2,4-三唑-4-基)苯和5-芳基三氮烯-1-基-1-苯基-1-吡唑-4-腈衍生物。通过5-氨基吡唑-4-腈与芳基重氮氯化物之间的偶联反应以中等产率获得三氮烯,其结构通过在红外光谱和碳核磁共振光谱中检测氰基官能团得以确认。相反,新型1,4-双(3,5-二烷基-4-1,2,4-三唑-4-基)苯衍生物是通过一条以前未报道的简便途径合成的,该途径从对苯二胺开始,与选定的原烷基三乙酯反应,然后与水合肼反应,接着在原烷基三乙酯中回流。甲基衍生物的结构通过X射线分析得以确认。对合成的化合物作为抗菌剂进行了测试和评估。