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Phosphorus oxychloride → 1-Chloro-4-cyclopropylisoquinoline

HRID 1852214
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HRID 1852214 반응식
[CH:1]1([C:4]2[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[CH:7]=[N+:6]([O-])[CH:5]=2)[CH2:3][CH2:2]1.O=P(Cl)(Cl)[Cl:17]>>[Cl:17][C:7]1[C:8]2[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:4]([CH:1]2[CH2:3][CH2:2]2)=[CH:5][N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 86683265Isoquinoline, 4-cyclopropyl-, 2-oxide

생성물 1

HCID 717427191-Chloro-4-cyclopropylisoquinoline수율 5.76%

실험 절차

A solution of 4-cyclopropylisoquinoline-2-oxide (0.3 g, 1.620 mmol) in POCl3 (15 ml) was refluxed for overnight. The solvent was evaporated under reduced pressure and the residue was diluted with cold water. The aqueous solution was basified by solid sodium carbonate and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to get crude compound. The crude compound was purified by silica gel chromatography (10% ethyl acetate in pet ether) to get the desired compound (0.02 g, 5.76%) as oil. 1H NMR (400 MHz, CDCl3): δ ppm 8.37-8.35 (d, J=8 Hz, 2H), 8.08 (s, 1H), 7.81 (t, J=8 Hz, 1H), 7.70 (t, J=4 Hz, 1H), 2.18 (m, 1H), 1.11 (t, J=4 Hz, 2H), 0.80 (t, J=8 Hz, 2H); MS: MS m/z 204.28 (M++1).

후처리

  • customThe solvent was evaporated under reduced pressure
  • additionthe residue was diluted with cold water
  • extractionextracted with ethyl acetate
  • dry with materialThe organic layer was dried over anhydrous sodium sulfate
  • filtrationfiltered
  • customevaporated under reduced pressure
  • customto get crude compound
  • customThe crude compound was purified by silica gel chromatography (10% ethyl acetate in pet ether)
  • 출처 및 근거

    ORD 기록
    ord-8b03193590bb47a4b29400c2e02d1e03
    출처 데이터셋
    uspto-grants-2015_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08957203B2

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