Solvent-free one-pot reactions for annulating a pyrimidine ring on thiazoles under microwave irradiation
โ Scribed by Lal Dhar S Yadav; Suman Dubey; Beerendra S Yadav
- Book ID
- 104205492
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 150 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0040-4020
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โฆ Synopsis
One-pot reactions of glycine, acetic anhydride and thiazole Schiff bases (2a -f) diastereoselectively and expeditiously annulate a pyrimidine ring on the thiazole nucleus to yield 6,7-dihydro-5H-thiazolo[3,2-a]pyrimidin-5-ones (4a -f) under microwave irradiation and solvent-free conditions.
๐ SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
The one-pot, three-component condensation of benzil, benzonitrile derivatives and primary amines on the surface of silica gel under solvent-free conditions and microwave irradiation provided tetrasubstituted imidazoles in high yields.
A rapid one-pot synthesis of imidazo[ 1,2-a] annulated pyridines, pyrazines and pyrimidines is described that occurs in the presence of recyclable montmorillonite K IO clay under solvent-free conditions using microwave irradiation.