反応 #2298621

ord-867ac4ad339d4d5ba9c5951f2f52e8fb

反応方程式

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
収率 82.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度at reflux for 1 hour
  2. 2
    抽出The aqueous mixture was extracted with ethyl acetate
  3. 3
    洗浄The organic layer was washed with water
  4. 4
    乾燥dried over anhydrous magnesium sulfate
  5. 5
    その他the solvent evaporated under reduced pressure

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: USRE039267E1uspto-grants-2006_09