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Phosphorus oxychloride → 1-Chloro-3-(4-fluorophenyl)-6-methoxyisoquinoline

HRID 1852099
ノート
印刷プレビュー

反応式

HRID 1852099 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]=[C:10](O)[C:11]3[C:16]([CH:17]=2)=[CH:15][C:14]([O:18][CH3:19])=[CH:13][CH:12]=3)=[CH:4][CH:3]=1.O=P(Cl)(Cl)[Cl:23]>>[Cl:23][C:10]1[C:11]2[C:16](=[CH:15][C:14]([O:18][CH3:19])=[CH:13][CH:12]=2)[CH:17]=[C:8]([C:5]2[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=2)[N:9]=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 178487731HCID 178487731、化合物

生成物 1

HCID 866831881-Chloro-3-(4-fluorophenyl)-6-methoxyisoquinoline収率 91%

実験手順

A solution of 3-(4-fluorophenyl)-6-methoxyisoquinolin-1-ol (350 mg, 1.300 mmol) in POCl3 (1.82 ml, 19.50 mmol) was refluxed (90° C.) for 4 h. The reaction mixture was concentrated. The residue was dissolved in DCM and the pH was adjusted to 7 with 4N NaOH. The organic phase was collected and dried over sodium sulfate, filtered, then concentrated under vacuum. The crude material was purified by silica gel chromatography using 50% DCM in Hexanes as eluent. The product fractions were collected and the solvent removed under vacuum to give 1-chloro-3-(4-fluorophenyl)-6-methoxyisoquinoline (340 mg, 91% yield). MS: MS m/z 288.1 (M++1).

後処理

  1. concentrationThe reaction mixture was concentrated
  2. dissolution
The residue was dissolved in DCM
  • customThe organic phase was collected
  • dry with materialdried over sodium sulfate
  • filtrationfiltered
  • concentrationconcentrated under vacuum
  • customThe crude material was purified by silica gel chromatography
  • customThe product fractions were collected
  • customthe solvent removed under vacuum
  • 出典と根拠

    ORDレコード
    ord-5e28e66a1ebc486a85b98ca6c29af0e3
    出典データセット
    uspto-grants-2015_02
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08957203B2

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