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Sodium Methoxide → 7-Fluoro-2-methoxy-8-methylquinoxaline

HRID 2233167
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HRID 2233167 반응식
Cl[C:2]1[CH:11]=[N:10][C:9]2[C:4](=[C:5]([CH3:13])[C:6]([F:12])=[CH:7][CH:8]=2)[N:3]=1.[CH3:14][O-:15].[Na+]>CO>[F:12][C:6]1[C:5]([CH3:13])=[C:4]2[C:9]([N:10]=[CH:11][C:2]([O:15][CH3:14])=[N:3]2)=[CH:8][CH:7]=1
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참가 물질

4

반응물 2

HCID 10942334Sodium MethoxideHCID 866283592-Chloro-7-fluoro-8-methylquinoxaline

생성물 1

HCID 675481507-Fluoro-2-methoxy-8-methylquinoxaline수율 96%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

2-Chloro-7-fluoro-8-methylquinoxaline (4.1 g, 20.9 mmol) was suspended in dry methanol and a 25% solution of sodium methoxide in methanol (4.73 ml, 21.9 mmol) was added by syringe. The mixture was heated under reflux for 2 h, then evaporated. The residue was dissolved in dichloromethane and water and the phases were separated. The aqueous phase was extracted twice with dichloromethane, and combined organic fractions were dried and evaporated to give product (3.84 g, 96%).

후처리

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 2 h
  3. customevaporated
  4. dissolutionThe residue was dissolved in dichloromethane
  5. customwater and the phases were separated
  6. extractionThe aqueous phase was extracted twice with dichloromethane
  7. customwere dried
  8. customevaporated

출처 및 근거

ORD 기록
ord-a142b70347a1436ba085ad7f7903088e
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07709483B2

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