Ethyl Acetate → alpha-(5-BRomo-1,3-benzodioxol-4-yl)-5-isoquinolinemethanol

HRID 8711

반응식

HRID 8711 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]2[O:8][CH2:9][O:10][C:4]=2[CH:3]=1.C([N-]C(C)C)(C)C.[Li+].[CH:19]1[C:28]2[CH:27]=[CH:26][CH:25]=[C:24]([CH:29]=[O:30])[C:23]=2[CH:22]=[CH:21][N:20]=1.CCOC(C)=O>C1COCC1>[Br:1][C:2]1[CH:7]=[CH:6][C:5]2[O:8][CH2:9][O:10][C:4]=2[C:3]=1[CH:29]([C:24]1[C:23]2[CH:22]=[CH:21][N:20]=[CH:19][C:28]=2[CH:27]=[CH:26][CH:25]=1)[OH:30]

참가 물질

6

반응 조건

온도
-78 °C

실험 절차

To a solution of 4-bromo-1,2-(methylendioxy)benzene (3.01 g, 15 mmol) in THF (20 mL) at −78° C. was added dropwise lithium diisopropylamide (10.6 mL of 1.5 M in cyclohexane, 16 mmol). The reaction mixture was stirred at −78° C. under argon for 20 minutes. A brown solution was formed. A solution of 5-isoquinolinecarboxaldehyde (1.90 g, 12 mmol) in THF (4 mL) was added dropwise. The resulting mixture was stirred at −78° C. for 10 minutes and warmed to room temperature. Stirring was continued for 30 minutes at room temperature, and then the mixture was quenched with saturated NH4Cl solution. The product was extracted with EtOAc and the solvent was removed under reduced pressure. Chromatography (SiO2 Type-H, 35% EtOAc in Hexanes) of the residue yielded the title compound as a yellow solid (2.8 g, 7.8 mmol, 65% yield): mp 173–175° C.;

후처리

  1. customA brown solution was formed
  2. stirringThe resulting mixture was stirred at −78° C. for 10 minutes
  3. temperaturewarmed to room temperature
  4. stirringStirring
  5. waitwas continued for 30 minutes at room temperature
  6. customthe mixture was quenched with saturated NH4Cl solution
  7. extractionThe product was extracted with EtOAc
  8. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-d7ba93572fa64fddbb46271e8f729e27
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07091212B2

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