Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5283559 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
Pyridopyrimidine-spirocyclohexanetriones (5, 6) and pyrimido[4,5-b]quinolinones (8) were obtained in a three-component microwave-assisted reaction of 6-aminopyrimidin-4-ones (1) with dimedone (2) and formaldehyde solution or paraformaldehyde, respectively. A mechanism is proposed based on the presence of a basic catalyst (triethylamine in this case) and the fact that single condensation intermediates are isolated prior to the cyclization leading to the final products.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jairo Quiroga, Silvia Cruz, Braulio Insuasty, Rodrigo AbonÃa, Manuel Nogueras, Justo Cobo,