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Phosphorus oxychloride → 1-Chloro-4-phenyl-isoquinoline-3-carboxylic acid ethyl ester

HRID 1866393
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반응식

HRID 1866393 반응식
[CH2:1]([O:3][C:4]([C:6]1[N:7]=[C:8](O)[C:9]2[C:14]([C:15]=1[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[CH:13][CH:12]=[CH:11][CH:10]=2)=[O:5])[CH3:2].O=P(Cl)(Cl)[Cl:25]>>[CH2:1]([O:3][C:4]([C:6]1[N:7]=[C:8]([Cl:25])[C:9]2[C:14]([C:15]=1[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[CH:13][CH:12]=[CH:11][CH:10]=2)=[O:5])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178470308HCID 178470308, 화합물

생성물 1

HCID 860146021-Chloro-4-phenyl-isoquinoline-3-carboxylic acid ethyl ester

실험 절차

A mixture of 1-hydroxy-4-phenyl-isoquinoline-3-carboxylic acid ethyl ester (1.17 g, 4 mmol; can be obtained according to A. Marsili et al., Ann. Chim. (Rome), 1962, 52, 112-120), and concentrated POCl3 (10 ml) was refluxed with stirring for 1 h. Then the mixture was concentrated in vacuo. The residue was dissolved in EtOAc (50 ml), concentrated aqueous NaHCO3 solution (40 ml) was added and the mixture was stirred vigorously for 1 h. Subsequently, the organic phase was separated, dried over MgSO4 and concentrated in vacuo to give the title compound as a yellowish solid (1.20 g); MS-(+)-ion: M+1=312.0.

후처리

  1. customcan be obtained
  2. concentrationThen the mixture was concentrated in vacuo
  3. dissolution
The residue was dissolved in EtOAc (50 ml)
  • additionconcentrated aqueous NaHCO3 solution (40 ml) was added
  • stirringthe mixture was stirred vigorously for 1 h
  • customSubsequently, the organic phase was separated
  • dry with materialdried over MgSO4
  • concentrationconcentrated in vacuo
  • 출처 및 근거

    ORD 기록
    ord-5bf26197bffe4939a34337bcfd61a978
    출처 데이터셋
    uspto-grants-2009_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07629357B2

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