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机构地区:[1]Department of Medicinal Chemistry, China Pharmaceutical University, Nanjing 210009, China
出 处:《Chinese Chemical Letters》2007年第6期647-650,共4页中国化学快报(英文版)
摘 要:An efficient synthesis of 3,4-dihydropyrimidin-2(1H)-one derivatives using formic acid as catalyst, from aldehydes, β-ketoester and urea(thiourea) without solvent under the irradiation of microwave is described. Compared with the classical Biginelli reaction, this new method has the advantage of good yields (77–94% for aromatic aldehydes) and short reaction time (3–8 min).An efficient synthesis of 3,4-dihydropyrimidin-2(1H)-one derivatives using formic acid as catalyst, from aldehydes, β-ketoester and urea(thiourea) without solvent under the irradiation of microwave is described. Compared with the classical Biginelli reaction, this new method has the advantage of good yields (77–94% for aromatic aldehydes) and short reaction time (3–8 min).
关 键 词:Biginelli reaction 3 4-Dihydropyrimidone MICROWAVE SOLVENT-FREE Formic acid
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