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Phosphorus tribromide → 4-(1-Bromopropan-2-yloxy)-7-methoxyquinoline

HRID 1878698
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HRID 1878698 반응식
COC1C=C2C(C(OCC(O)C)=CC=N2)=CC=1.[CH3:18][O:19][C:20]1[CH:29]=[C:28]2[C:23]([C:24]([O:30][CH:31]([CH3:34])[CH2:32]O)=[CH:25][CH:26]=[N:27]2)=[CH:22][CH:21]=1.P(Br)(Br)[Br:36]>C(Cl)Cl>[Br:36][CH2:32][CH:31]([O:30][C:24]1[C:23]2[C:28](=[CH:29][C:20]([O:19][CH3:18])=[CH:21][CH:22]=2)[N:27]=[CH:26][CH:25]=1)[CH3:34]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24614Phosphorus tribromideHCID 688094362-(7-Methoxyquinolin-4-yloxy)propan-1-olHCID 688118821-(7-Methoxyquinolin-4-yloxy)propan-2-ol

생성물 1

HCID 598430804-(1-Bromopropan-2-yloxy)-7-methoxyquinoline

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a stirred solution of 1-(7-methoxyquinolin-4-yloxy)propan-2-ol (235 mg, 1007 μmol) and 2-(7-methoxyquinolin-4-yloxy)propan-1-ol (235 mg, 1007 μmol) (mixture of isomers) in CH2Cl2 (3 mL) was added phosphorus tribromide (94.7 μl, 1007 μmol). The mixture was heated to reflux for 18 h. The mixture was quenched with 5% NaHCO3, and was extracted with CH2Cl2 (3×5 mL). The combined organics were dried over MgSO4 and concentrated to a white solid (150 mg) under reduced pressure. MS (ESI pos. ion) m/z (MH+): 296/298. Calc'd exact mass for C13H14BrNO2: 295.

후처리

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 18 h
  3. customThe mixture was quenched with 5% NaHCO3
  4. extractionwas extracted with CH2Cl2 (3×5 mL)
  5. dry with materialThe combined organics were dried over MgSO4
  6. concentrationconcentrated to a white solid (150 mg) under reduced pressure

출처 및 근거

ORD 기록
ord-7600bbd846b942b7be1d7395ff57d139
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08314087B2

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