반응 #2298621

ord-867ac4ad339d4d5ba9c5951f2f52e8fb

반응 방정식

O=c1[nH]cnc2c(Br)csc12
7-bromo-3H-thieno[3,2-d]pyrimid-4-one
O=c1[nH]cnc2c(Br)csc12
7-Bromo-3H-thieno[3,2-d]pyrimid-4-one
O=P(Cl)(Cl)Cl
phosphorus oxychloride
O=C([O-])O.[Na+]
sodium bicarbonate
Clc1ncnc2c(Br)csc12
7-bromo-4-chlorothieno[3,2-d]pyrimidine
수율 82.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도at reflux for 1 hour
  2. 2
    추출The aqueous mixture was extracted with ethyl acetate
  3. 3
    세척The organic layer was washed with water
  4. 4
    건조dried over anhydrous magnesium sulfate
  5. 5
    기타the solvent evaporated under reduced pressure

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE039267E1uspto-grants-2006_09