Generation of pyrrolo[2,3-d]pyrimidines. Unexpected products in the multicomponent reaction of 6-aminopyrimidines, dimedone, and arylglyoxal
✍ Scribed by Jairo Quiroga; Paola A. Acosta; Silvia Cruz; Rodrigo Abonía; Braulio Insuasty; Manuel Nogueras; Justo Cobo
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- French
- Weight
- 857 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
A series of 6-aryl-5-(1-cyclohexen-1-yl)pyrrolo[2,3-d]pyrimidines 9a-q were obtained by the three-component reaction between 6-aminopyrimidines 6, 7, 8, dimedone 2, and arylglyoxal 5a,b. The unexpected cyclization process was established by NMR and X-ray diffraction measurements.
📜 SIMILAR VOLUMES
pyridines 4a-e was prepared by the reaction of 5-ethylthio-1,3,4-thiadiazole-2-amine (1) and p-substituted 3-(dimeth-1,3,4-Thiadiazoles find a variety of applications as antibiotic, antiinflammatory or bacteriostatic agents and as pesticides [1] [2] . These biological activities have stimulated us t