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Phosphorus oxychloride → 1-Chloro-4-cyclopropylisoquinoline

HRID 1852214
ノート
印刷プレビュー

反応式

HRID 1852214 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

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

生成物 1

HCID 717427191-Chloro-4-cyclopropylisoquinoline収率 5.76%

実験手順

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).

後処理

  • 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)
  • 出典と根拠

    ORDレコード
    ord-8b03193590bb47a4b29400c2e02d1e03
    出典データセット
    uspto-grants-2015_02
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08957203B2

    反応ノート

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