Methanol → Methyl 6-bromo-3-methoxypyrazine-2-carboxylate

HRID 392302노트

반응식

HRID 392302 반응식
N[C:2]1[C:3]([C:9]([O:11][CH3:12])=[O:10])=[N:4][C:5]([Br:8])=[CH:6][N:7]=1.N([O-])=O.[Na+].[CH3:17][OH:18].C(Cl)(Cl)Cl>S(=O)(=O)(O)O>[Br:8][C:5]1[N:4]=[C:3]([C:9]([O:11][CH3:12])=[O:10])[C:2]([O:18][CH3:17])=[N:7][CH:6]=1

참가 물질

6

실험 절차

In 100 mL of concentrated sulfuric acid was dissolved 17.0 g of methyl 3-amino-6-bromo-2-pyrazinecarboxylate. At an ice-cooled temperature, 10.1 g of sodium nitrite was added and stirred for 30 minutes. The reaction mixture was poured into 920 mL of methanol and heated under reflux for 5 hours. After cooling the reaction mixture, the mixture was concentrated under reduced pressure, the residue thus obtained was added to a mixture of 500 mL of ice water and 600 mL of chloroform, and the mixture thus obtained was separated into layers. The organic layer was washed successively with a saturated aqueous solution of sodium hydrogen carbonate, water and saturated aqueous solution of sodium chloride and dried on anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. Thus, 6.30 g of methyl 6-bromo-3-methoxy-2-pyrazinecarboxylate was obtained as a light yellow oily product.

후처리

  1. additionwas added
  2. temperatureheated
  3. temperatureunder reflux for 5 hours
  4. temperatureAfter cooling the reaction mixture
  5. concentrationthe mixture was concentrated under reduced pressure
  6. customthe residue thus obtained
  7. customthe mixture thus obtained
  8. customwas separated into layers
  9. washThe organic layer was washed successively with a saturated aqueous solution of sodium hydrogen carbonate, water and saturated aqueous solution of sodium chloride
  10. dry with materialdried on anhydrous magnesium sulfate
  11. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-84efbb9db5f848ffa122de7edde43949
출처 데이터셋
uspto-grants-2004_10
특허 번호
US06800629B2

반응 노트

불러오는 중…