New access to thiazolo[4,5-d]pyrimidine derivativess
✍ Scribed by M. Bakavoli; M. Nikpour; M. Rahimizadeh
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2006
- Tongue
- English
- Weight
- 181 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Cl
1 -R 2 NH, EtOH, heat 2 -NaNH 2 , DMF, R'NCS R'
4-Amino-5-bromo-2-substituted-aminopyrimidines are readily obtained from the newly prepared 5bromo-2,4-dichloro-6-methylpyrimidine by sequential treatment with ethanolic ammonia and secondary amines. These compounds were successfully reacted with various isothiocyanates in the presence of sodamide in DMF to form the new thiazolo [4,5-d] pyrimidine derivatives .
📜 SIMILAR VOLUMES
## Abstract Several 2‐substituted 7‐mercapto‐thiazolo[5,4‐d]pyrimidines were synthesized from 4,6‐dimercapto‐5‐amino‐pyrimidines by reaction with acid anhydrides or mid chlorides.