(E)-1-(4-Methoxyphenyl)-5-methyl-4-(1-phenyl-4-((2-(2,4,6-trichlorophenyl)hydrazineylidene)methyl)-1H-pyrazol-3-yl)-1H-1,2,3-triazole

Molbank Pub Date : 2024-03-28 DOI:10.3390/m1798
Bakr F. Abdel-Wahab, Hanan A. Mohamed, B. Kariuki, Gamal A. El-Hiti
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引用次数: 0

Abstract

The reaction of equimolar quantities of 3-(1-(4-methoxyphenyl)-5-methyl-1H-1,2,3-triazol-4-yl)-1-phenyl-1H-pyrazole-4-carbaldehyde and (2,4,6-trichlorophenyl)hydrazine in ethanol containing concentrated hydrochloric acid (0.2 mL; 37%) as a catalyst under reflux for 2 h yielded 1-(1-(benzofuran-2-yl)ethylidene)-2-(2,4,6-trichlorophenyl)hydrazine. The crude produced was purified by crystallization using dimethylformamide to provide the title heterocycle in a 95% yield. The structure of the newly synthesized heterocycle was confirmed through X-ray diffraction and spectral analyses.
(E)-1-(4-甲氧基苯基)-5-甲基-4-(1-苯基-4-((2-(2,4,6-三氯苯基)亚肼)甲基)-1H-吡唑-3-基)-1H-1,2,3-三唑
等摩尔量的 3-(1-(4-甲氧基苯基)-5-甲基-1H-1,2,3-三唑-4-基)-1-苯基-1H-吡唑-4-甲醛和(2,4,6-三氯苯基)肼在含有浓盐酸(0.2 mL; 37%) 作为催化剂,回流 2 小时,得到 1-(1-(苯并呋喃-2-基)亚乙基)-2-(2,4,6-三氯苯基)肼。通过使用二甲基甲酰胺进行结晶提纯,得到了标题杂环,收率为 95%。通过 X 射线衍射和光谱分析,确认了新合成杂环的结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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