## Abstract Careful α‐bromination of ketones with elemental bromine and direct addition of pyrimidine‐2‐thiones and triethylamine renders possible a direct two‐step one‐pot synthesis of the title compounds.
Convenient method for synthesis of thiazolo[3,2-a]pyrimidine derivatives in a one-pot procedure
✍ Scribed by Sukhdeep Singh; Andreas Schober; Michael Gebinoga; G. Alexander Groß
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- French
- Weight
- 458 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
An efficient one-pot method to synthesize thiazolo[3,2-a]pyrimidine derivatives has been developed. The method involves the temperature controlled functionalization-annulation of 5-ethoxycarbonyl-6methyl-4-aryl-3,4-dihydro-2(1H)-pyrimidin-2-thione (DHPM) derivatives with in-situ generated bromo-ketones received by reaction of different a-H carbonyl compounds with bromine.
📜 SIMILAR VOLUMES
## Abstract A new class of spiro thiazolo[3,2‐__a__]pyrimidine compounds were synthesized by the one‐pot sequential 1,3‐dipolar cycloaddition of azomethine ylide (generated from isatin and sarcosine)–nitrile oxide to 2‐arylmethylidene‐6,7‐dihydro‐5__H__‐thiazolo[3,2‐__a__]pyrimidin‐3‐ones in modera