Abstract
The substituted 3,4-dihydropyrimidin-2(1H)-ones and their thione analogues have been prepared Via Biginelli condensation using aldehyde, 1,3-dicarbonyl compound and urea or thiourea under the catalyst of sulphamic acid (H2NSO3H). The method is simple, cost-effective, and gives good yields in a shorter reaction time.
Keywords: sulphamic acid, catalyst, biginelli reaction
Letters in Organic Chemistry
Title: Sulphamic Acid (H2NSO3H) Catalysed One Pot Synthesis of 3,4-Dihydropyrimidin-2(1h)-Ones and their Thione Analogues
Volume: 2 Issue: 7
Author(s): S. A. Kotharkar, M. R. Jadhav, R. R. Nagawade, S. S. Bahekar and D. B. Shinde
Affiliation:
Keywords: sulphamic acid, catalyst, biginelli reaction
Abstract: The substituted 3,4-dihydropyrimidin-2(1H)-ones and their thione analogues have been prepared Via Biginelli condensation using aldehyde, 1,3-dicarbonyl compound and urea or thiourea under the catalyst of sulphamic acid (H2NSO3H). The method is simple, cost-effective, and gives good yields in a shorter reaction time.
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Cite this article as:
Kotharkar A. S., Jadhav R. M., Nagawade R. R., Bahekar S. S. and Shinde B. D., Sulphamic Acid (H2NSO3H) Catalysed One Pot Synthesis of 3,4-Dihydropyrimidin-2(1h)-Ones and their Thione Analogues, Letters in Organic Chemistry 2005; 2 (7) . https://dx.doi.org/10.2174/157017805774296830
DOI https://dx.doi.org/10.2174/157017805774296830 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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