Réaction #2298615
ord-fed04a0ceb4d4011a69766e44f8a3bec
Équation de réaction
7-methyl-3H-thieno[3,2-d]pyrimid-4-one
7-Methyl-3H-thieno[3,2-d]pyrimid-4-one
phosphorus oxychloride
sodium bicarbonate
→
4-chloro-7-methylthieno[3,2-d]pyrimidine
Rendement 96.0%
Réactifs
Réactifs
Aucun
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Températureat reflux for 1 hour
- 2ExtractionThe aqueous mixture was extracted with diethyl ether
- 3LavageThe organic layer was washed with water
- 4Séchagedried over anhydrous magnesium sulfate
- 5Autrethe solvent evaporated under reduced pressure
Mode opératoire
A solution of 7-methyl-3H-thieno[3,2-d]pyrimid-4-one (3, 2.9 g, 18 mmol) in phosphorus oxychloride (18 mL) under N2 was heated at reflux for 1 hour. The resulting solution as allowed to cool to room temperature and then poured into a saturated aqueous solution of sodium bicarbonate to neutralize. The aqueous mixture was extracted with diethyl ether. The organic layer was washed with water followed by saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and the solvent evaporated under reduced pressure to yield 4-chloro-7-methylthieno[3,2-d]pyrimidine (3.1 g, 96% yield) as a white solid.