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Water → 4-(6-Hydroxy-3-methylquinolin-2-yl)benzoic acid

HRID 2201411
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HRID 2201411 반응식
C[O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[C:8]([C:13]1[CH:22]=[CH:21][C:16]([C:17]([O:19]C)=[O:18])=[CH:15][CH:14]=1)[C:7]([CH3:23])=[CH:6]2.B(Br)(Br)Br.O>C(Cl)Cl>[OH:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[C:8]([C:13]1[CH:14]=[CH:15][C:16]([C:17]([OH:19])=[O:18])=[CH:21][CH:22]=1)[C:7]([CH3:23])=[CH:6]2
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참가 물질

5

반응물 3

HCID 962WaterHCID 25134Boron tribromideHCID 66980055Methyl 4-(6-methoxy-3-methylquinolin-2-yl)benzoate

생성물 1

HCID 569607734-(6-Hydroxy-3-methylquinolin-2-yl)benzoic acid수율 28.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Methyl 4-(6-methoxy-3-methylquinolin-2-yl)benzoate (37 mg, 0.121 mmol) was dissolved in 2 mL of DCM and BBr3 (150 μL) was added. The mixture was stirred at room temperature for 1 day followed by addition of 10 mL of H2O. The solution was stirred vigorously for 1 h followed by filtration of the solids. The solids were washed with H2O and dried in vacuo to yield 9.5 mg (28% yield) of Compound IV-1. 1H NMR (DMSO-d6, 400 MHz): δ 8.37 (s, 1H), 8.10 (d, 2H), 7.94 (d, 1H), 7.78 (d, 2H), 7.42-7.39 (dd, 1H), 7.24-7.23 (d, 1H), 2.43 (s, 3H). MS (ESI): m/z 280.10 [M+H]+.

후처리

  1. stirringThe solution was stirred vigorously for 1 h
  2. filtrationfollowed by filtration of the solids
  3. washThe solids were washed with H2O
  4. customdried in vacuo

출처 및 근거

ORD 기록
ord-2e5c0ce9e63941f0bc0c894e6b07579e
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09364481B2

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