Three component reactions: An efficient and green synthesis of 3,4-dihydropyrimidin-2-(1H)-ones and thiones using silica gel-supported l-pyrrolidine-2-carboxylic acid-4-hydrogen sulfate

An environmentally benign aqueous protocol for the synthesis of 3,4-dihydropyrimidin-2-(1H)-ones and thiones promoted by a green catalyst, silica gel-supported l-pyrrolidine-2-carboxylic acid-4-hydrogen sulfate, has been developed. The use of nontoxic, thermally stable and inexpensive amino acid catalyst makes the process simple with minimal amount of chemical waste. Compared with classical Biginelli reaction conditions, this new method has the advantages of high yields and simple workup procedures.

Graphical abstractSilica gel-supported l-pyrrolidine-2-carboxylic acid-4-hydrogen sulfate as a green organocatalyst has been introduced for the synthesis of 3,4-dihydropyrimidin-2-(1H)-ones and thiones.Figure optionsDownload full-size imageDownload as PowerPoint slide