Abstract
The condensation reactions of alkyl isocyanides with 1,3-dimethylbarbituric acid and aryl carboxaldehydes to afford 6-(alkylamino)-5-(3-aryl)-1,3-dimethylfuro[2,3-d]pyrimidine-2,4(1H,3H)-dione, in excellent yields under neutral conditions, are reported.
Keywords: Aldehydes, condensation reaction, fused heterocycles, isocyanides, 1,3-dimethylbarbituric acid, 1,3-dimethylfuro[2,3-d]pyrimidine, N-methyl groups, anti-inflammatory, antiviral, anti HIV
Letters in Organic Chemistry
Title: Three Component Condensation Reaction as an Efficient Route for the Synthesis of Furo[2,3-d]pyrimidines
Volume: 9 Issue: 1
Author(s): Ali Aminkhani and Ghasem Marandi
Affiliation:
Keywords: Aldehydes, condensation reaction, fused heterocycles, isocyanides, 1,3-dimethylbarbituric acid, 1,3-dimethylfuro[2,3-d]pyrimidine, N-methyl groups, anti-inflammatory, antiviral, anti HIV
Abstract: The condensation reactions of alkyl isocyanides with 1,3-dimethylbarbituric acid and aryl carboxaldehydes to afford 6-(alkylamino)-5-(3-aryl)-1,3-dimethylfuro[2,3-d]pyrimidine-2,4(1H,3H)-dione, in excellent yields under neutral conditions, are reported.
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Cite this article as:
Aminkhani Ali and Marandi Ghasem, Three Component Condensation Reaction as an Efficient Route for the Synthesis of Furo[2,3-d]pyrimidines, Letters in Organic Chemistry 2012; 9 (1) . https://dx.doi.org/10.2174/157017812799304079
DOI https://dx.doi.org/10.2174/157017812799304079 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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