Abstract
An efficient and simple protocol has been developed for the synthesis of 3,4-dihydropyrimidin-2-(1H)-ones by a one-pot three-component cyclocondensation reaction of an aromatic aldehyde, β-ketoester, and urea or thiourea under solvent-free conditions using triethylamine (Et3N) as catalyst for the Biginelli reaction.
Keywords: Triethylamine, Bronsted bases, multicomponent reaction, 3,4-dihydropyrimidin-2(1H)-ones/thiones, Biginelli reaction, one-pot condensation
Letters in Organic Chemistry
Title: Triethylamine Promoted Efficient Synthesis of 3,4-Dihydropyrimidin- 2(1H)-ones/thiones Using a Solvent-Free Biginelli Condensation
Volume: 7 Issue: 4
Author(s): Abdelmadjid Debache, Wassima Ghalem, Raouf Boulcina, Ali Belfaitah, Salah Rhouati and Bertrand Carboni
Affiliation:
Keywords: Triethylamine, Bronsted bases, multicomponent reaction, 3,4-dihydropyrimidin-2(1H)-ones/thiones, Biginelli reaction, one-pot condensation
Abstract: An efficient and simple protocol has been developed for the synthesis of 3,4-dihydropyrimidin-2-(1H)-ones by a one-pot three-component cyclocondensation reaction of an aromatic aldehyde, β-ketoester, and urea or thiourea under solvent-free conditions using triethylamine (Et3N) as catalyst for the Biginelli reaction.
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Cite this article as:
Debache Abdelmadjid, Ghalem Wassima, Boulcina Raouf, Belfaitah Ali, Rhouati Salah and Carboni Bertrand, Triethylamine Promoted Efficient Synthesis of 3,4-Dihydropyrimidin- 2(1H)-ones/thiones Using a Solvent-Free Biginelli Condensation, Letters in Organic Chemistry 2010; 7 (4) . https://dx.doi.org/10.2174/157017810791130595
DOI https://dx.doi.org/10.2174/157017810791130595 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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