Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, China.
J Org Chem. 2010 Feb 19;75(4):1162-7. doi: 10.1021/jo902394y.
An efficient one-pot synthesis of 4,5,6-triaryl-3,4-dihydropyrimidin-2(1H)-ones via a three-component Biginelli-type condensation of aldehyde, 2-phenylacetophenone, and urea/thiourea in the presence of a catalytic amount of t-BuOK (20 mol %) is described. The reactions proceeded efficiently at 70 degrees C to afford the desired products in moderate to good yields. Detailed mechanistic study shows that the Biginelli-type reaction using urea and thiourea proceeds through two totally different pathways. Enone 5 and bis-urea 8 were highly suggested as respective reaction intermediates for reactions involving thiourea and urea as substrates.
一种通过醛、2-苯乙酮和脲/硫脲的三组分Biginelli 型缩合反应,在催化量的叔丁醇钾(20mol%)存在下,高效合成 4,5,6-三芳基-3,4-二氢嘧啶-2(1H)-酮的有效一锅法。反应在 70°C 下高效进行,以中等至良好的产率得到所需产物。详细的机理研究表明,使用脲和硫脲的 Biginelli 型反应通过两种完全不同的途径进行。烯酮 5 和双脲 8 被高度认为是涉及硫脲和脲作为底物的反应的各自反应中间体。