Реакция #2298621

ord-867ac4ad339d4d5ba9c5951f2f52e8fb

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураat reflux for 1 hour
  2. 2
    ЭкстракцияThe aqueous mixture was extracted with ethyl acetate
  3. 3
    ПромывкаThe organic layer was washed with water
  4. 4
    Сушкаdried over anhydrous magnesium sulfate
  5. 5
    Другоеthe solvent evaporated under reduced pressure

Методика

A solution of 7-bromo-3H-thieno[3,2-d]pyrimid-4-one (126, 0.94 g, 4.1 mmol) in phosphorus oxychloride (4 mL) under N2 was heated at reflux for 1 hour. The resulting solution was 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 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 7-bromo-4-chlorothieno[3,2-d]pyrimidine (0.83 g, 82% yield) as a yellow solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE039267E1uspto-grants-2006_09