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Phosphorus oxychloride → 1-Chloro-7-methoxy-3-(2-methoxyphenyl)isoquinoline

HRID 1251148
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HRID 1251148 반응식
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[C:8]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[O:20][CH3:21])[N+:9]([O-])=[CH:10]2)=[CH:5][CH:4]=1.P(Cl)(Cl)([Cl:24])=O>>[Cl:24][C:10]1[C:11]2[C:6](=[CH:5][CH:4]=[C:3]([O:2][CH3:1])[CH:12]=2)[CH:7]=[C:8]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[O:20][CH3:21])[N:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 225035447-Methoxy-3-(2-methoxyphenyl)isoquinoline-2-oxide

생성물 1

HCID 225036211-Chloro-7-methoxy-3-(2-methoxyphenyl)isoquinoline

실험 절차

7-Methoxy-3-(2-methoxyphenyl)isoquinoline-2-oxide (0.60 g) and phosphorus oxychloride (5 ml) were reacted at 110° C. for 2 hr. The reaction solution was concentrated, and to the resulting residue were added ethyl acetate and an aqueous saturated sodium bicarbonate. The resulting organic layer was washed with water and brine, and dried over magnesium sulfate. The solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane system), to give 0.56 g of the title compound as a white solid.

후처리

  1. concentrationThe reaction solution was concentrated
  2. additionto the resulting residue were added ethyl acetate
wash
The resulting organic layer was washed with water and brine
  • dry with materialdried over magnesium sulfate
  • customThe solvent was evaporated
  • customthe resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane system)
  • 출처 및 근거

    ORD 기록
    ord-21aa46679e874c0dae716cf17dd51eb8
    출처 데이터셋
    uspto-grants-2002_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06340759B1

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