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Phosphorus oxychloride → 1-chloro-6-methoxy-N,N-dimethylisoquinolin-3-amine

HRID 1852103
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反応式

HRID 1852103 の反応式
[CH3:1][N:2]([CH3:16])[C:3]1[N:4]=[C:5](O)[C:6]2[C:11]([CH:12]=1)=[CH:10][C:9]([O:13][CH3:14])=[CH:8][CH:7]=2.O=P(Cl)(Cl)[Cl:19]>>[Cl:19][C:5]1[C:6]2[C:11](=[CH:10][C:9]([O:13][CH3:14])=[CH:8][CH:7]=2)[CH:12]=[C:3]([N:2]([CH3:16])[CH3:1])[N:4]=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 178487765HCID 178487765、化合物

生成物 1

HCID 594234521-chloro-6-methoxy-N,N-dimethylisoquinolin-3-amine収率 53%

実験手順

A solution of 3-(dimethylamino)-6-methoxyisoquinolin-1-ol (700 mg, 3.21 mmol) in POCl3 (2 ml, 21.46 mmol) was refluxed 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 was removed under vacuum to give 1-chloro-6-methoxy-N,N-dimethylisoquinolin-3-amine (400 mg, 53% yield). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 7.96 (d, J=9.3 Hz, 1H), 6.87 (dd, J=9.2, 2.4 Hz, 1H), 6.80 (d, J=2.3 Hz, 1H), 6.43 (s, 1H), 3.91 (s, 3H), 3.14 (s, 6H); MS m/z 237.0 (M++1).

後処理

concentration
The reaction mixture was concentrated
  • dissolutionThe 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 was removed under vacuum
  • 出典と根拠

    ORDレコード
    ord-ef2830236b6a44c3acaf1161a8718682
    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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