Sodium hydride → 7-Chloro-6-(1,4-dioxa-spiro[4.5]dec-8-yloxy)-2-(4-methoxy-benzyl)-2H-isoquinolin-1-one
反応式
[O:1]1[C:5]2([CH2:10][CH2:9][CH:8]([OH:11])[CH2:7][CH2:6]2)CCO1.[H-].[Na+].[Cl:14][C:15]1[CH:24]=[C:23]2[C:18]([CH:19]=[CH:20][N:21]([CH2:26][C:27]3[CH:32]=[CH:31][C:30]([O:33][CH3:34])=[CH:29][CH:28]=3)[C:22]2=[O:25])=[CH:17][C:16]=1F.[CH3:36][C:37](N(C)C)=[O:38]>>[Cl:14][C:15]1[CH:24]=[C:23]2[C:18]([CH:19]=[CH:20][N:21]([CH2:26][C:27]3[CH:32]=[CH:31][C:30]([O:33][CH3:34])=[CH:29][CH:28]=3)[C:22]2=[O:25])=[CH:17][C:16]=1[O:11][CH:8]1[CH2:7][CH2:6][C:5]2([O:1][CH2:36][CH2:37][O:38]2)[CH2:10][CH2:9]1参加物
5
実験手順
1.49 g (9.44 mmol) of dioxa-spiro[4.5]decan-8-ol were dissolved in 30 ml of dimethyl acetamide and 283 mg (11.8 mmol) of sodium hydride (60%) were added. After stirring for 30 min at room temperature a solution of 2.50 g (7.87 mmol) of 7-chloro-6-fluoro-2-(4-methoxy-benzyl)-2H-isoquinolin-1-one (10) in 20 ml of dimethyl acetamide was added and stirring was continued at room temperature. After the reaction went to completion the solvent was removed under reduced pressure. The residue was dissolved in dichloromethane and washed with water. The organic layer was dried with magnesium sulfate and evaporated. Purification by silica gel chromatography yielded 1.84 g of the title compound. Rt=2.00 min (Method B). Detected mass: 456.1 (M+H+).
後処理
- additionwas added
- customwas continued at room temperature
- customwas removed under reduced pressure
- dissolutionThe residue was dissolved in dichloromethane
- washwashed with water
- dry with materialThe organic layer was dried with magnesium sulfate
- customevaporated
- customPurification by silica gel chromatography
出典と根拠
- ORDレコード
- ord-0de23a87067a4fe1896378e4471efaa6
- 出典データセット
- uspto-grants-2014_04
- 特許番号
- US08710077B2
反応ノート
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