1-(3,4-Dimethoxyphenyl)-3-(4-methoxyphenyl)-3-(1H-1,2,4-triazol-1-yl)propan-1-one

Molbank Pub Date : 2024-03-12 DOI:10.3390/m1791
Anna Nacher-Luis, Isidro M. Pastor
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Abstract

The study of new catalytic protocols for the synthesis of organic compounds with a more sustainable perspective is of interest. The use of ionic organic solids, such as 1,3-bis(carboxymethyl)imidazolium chloride as a catalyst has allowed the Michael addition of N-heterocycles to chalcones. This methodology has been applied to the unique preparation of the potential bioactive compound 1-(3,4-dimethoxyphenyl)-3-(4-methoxyphenyl)-3-(1H-1,2,4-triazol-1-yl)propan-1-one with moderate yield, due to the retro-Michael reaction. Both synthetic reactions (i.e., preparation of chalcone and triazole Michael-addition to chalcone) have good green metrics.
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1-(3,4-Dimethoxyphenyl)-3-(4-methoxyphenyl)-3-(1H-1,2,4-triazol-1-yl)propan-1-one
从更可持续的角度研究合成有机化合物的新催化方案很有意义。使用离子有机固体(如 1,3-双(羧甲基)氯化咪唑)作为催化剂,可以将 N-杂环与查耳酮进行迈克尔加成。通过逆迈克尔反应,这种方法被独特地应用于制备潜在的生物活性化合物 1-(3,4-二甲氧基苯基)-3-(4-甲氧基苯基)-3-(1H-1,2,4-三唑-1-基)丙-1-酮,产量适中。这两个合成反应(即制备查尔酮和三唑与查尔酮的迈克尔加成反应)都具有良好的绿色指标。
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