Reaktion #2298626

Reaktionsgleichung

6-(3-thienyl)-3H-thieno[3,2-d]pyrimid-4-one

6-(3-Thienyl)-3H-thieno[3,2-d]pyrimid-4-one

phosphorus oxychloride

sodium bicarbonate

→

6-(3-thienyl)-4-chlorothieno[3,2-d]pyrimidine

Ausbeute 81.0%

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturat reflux for 1 hour
2. 2
   Extraktionextracted with ethyl acetate
3. 3
   WaschenThe organic layer was washed with water
4. 4
   Trocknendried over anhydrous magnesium sulfate
5. 5
   Sonstigethe solvent evaporated under reduced pressure

Vorschrift

A solution of 6-(3-thienyl)-3H-thieno[3,2-d]pyrimid-4-one (218, 74 mg, 0.32 mmol) in phosphorus oxychloride (2 mL) under N2 was heated at reflux for 1 hour. The resulting solution was allowed to cool to room temperature, poured into a saturated aqueous solution of sodium bicarbonate to neutralize and then extracted with ethyl acetate. 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 6-(3-thienyl)-4-chlorothieno[3,2-d]pyrimidine (65 mg, 81% yield) as a yellow solid.

Quelle