Back to Search
Start Over
Functionalization of 2-Amino-3-benzyl-6-(benzylthio)pyrimidin-4(3H)-one: An Efficient Access to the Synthesis of Polycyclic Pyrimidine Scaffolds.
- Source :
-
Russian Journal of General Chemistry . Mar2020, Vol. 90 Issue 3, p489-492. 4p. 4 Diagrams. - Publication Year :
- 2020
-
Abstract
- 2-Aminouracil is used in the synthesis of a new series of tri- and tetracyclic pyrimidine scaffolds as the precursor. Thiazolo[5,4-d]triazolo[4,3-a]pyrimidine has been synthesized by diazotization and heterocyclization of the aminopyrimidinone derivative with nitrous acid at low temperature. Some new pyrimidines have been formed in the course of acylation and cyclization of the same compound with acetic anhydride, formic acid, pyruvic acid, or phthalic anhydride. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 10703632
- Volume :
- 90
- Issue :
- 3
- Database :
- Academic Search Index
- Journal :
- Russian Journal of General Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 142828240
- Full Text :
- https://doi.org/10.1134/S107036322003024X