Potassium Hydroxide → 6-Butoxy-7-methoxy-1-(3-methoxy-benzyl)-1,2-dihydro-isoquinoline-4-carbaldehyde
反応式
C(OC([N:6]1[CH:15]=[C:14]([CH:16]=[O:17])[C:13]2[C:8](=[CH:9][C:10]([O:23][CH3:24])=[C:11]([O:18][CH2:19][CH2:20][CH2:21][CH3:22])[CH:12]=2)[CH:7]1[CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[C:28]([O:32][CH3:33])[CH:27]=1)=O)C.[OH-].[K+]>CO>[CH2:19]([O:18][C:11]1[CH:12]=[C:13]2[C:8](=[CH:9][C:10]=1[O:23][CH3:24])[CH:7]([CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[C:28]([O:32][CH3:33])[CH:27]=1)[NH:6][CH:15]=[C:14]2[CH:16]=[O:17])[CH2:20][CH2:21][CH3:22]参加物
実験手順
To a stirred solution of 6-butoxy-4-formyl-7-methoxy-1-(3-methoxy-benzyl)-1H-isoquinoline-2-carboxylic acid ethyl ester (286 mg, 0.60 mmol) in methanol (12 mL) was added powdered potassium hydroxide (341 mg, 6.08 mmol). The reaction mixture was stirred at room temperature for 15 hrs. The solvent was evaporated and the residue was diluted with ethyl acetate (20 mL) and water (20 mL). The aqueous phase was extracted with ethyl acetate (3×20 mL). The combined extracts were washed with saturated aqueous sodium chloride solution (20 mL), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to afford 6-butoxy-7-methoxy-1-(3-methoxy-benzyl)-1,2-dihydro-isoquinoline-4-carbaldehyde (200 mg, 87% yield) as a yellow oil. The crude product was used without further purification.
後処理
- customThe solvent was evaporated
- additionthe residue was diluted with ethyl acetate (20 mL) and water (20 mL)
- extractionThe aqueous phase was extracted with ethyl acetate (3×20 mL)
- washThe combined extracts were washed with saturated aqueous sodium chloride solution (20 mL)
- dry with materialdried over anhydrous magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-e6b52869ffb5473c8e439ff7af742735
- 出典データセット
- uspto-grants-2006_06
- 特許番号
- US07067529B2
反応ノート
読み込み中…