Reaktion #9866

Reaktionsgleichung

4-chloro-2-methylsulfanyl-thieno[2,3-d]pyrimidine

OXONE

tetrahydrofuran

→

title compound

4—Chloro-2-methanesulfonyl-thieno[2,3-d]pyrimidine

Lösungsmittel

water

ethyl acetate

water

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturThe resulting mixture was gradually warmed from 0° C. to room temperature overnight
2. 2
   Sonstigethe layers were separated
3. 3
   ExtraktionThe aqueous layer was extracted with ethyl acetate (1×300 mL)
4. 4
   Waschenwashed with brine (2×300 mL)
5. 5
   Trocknendried over magnesium sulfate
6. 6
   Filtrationfiltered
7. 7
   Einengenconcentrated

Vorschrift

To a solution of 4-chloro-2-methylsulfanyl-thieno[2,3-d]pyrimidine (10 g, 46.15 mmol) in tetrahydrofuran (350 mL) at 0° C. was added a solution of OXONE (59.6 g, 2.1 eq) in water (300 mL) dropwise with stirring. The resulting mixture was gradually warmed from 0° C. to room temperature overnight. The reaction mixture was diluted with ethyl acetate (1000 mL) and water (300 mL), and the layers were separated. The aqueous layer was extracted with ethyl acetate (1×300 mL). Organic layers were combined, washed with brine (2×300 mL), dried over magnesium sulfate, filtered and concentrated to give 10.7 g of the title compound as a tan powder (M+H)+=249.

Quelle