反応式
[CH3:1][O:2][C:3]1[C:4]([O:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH2:9][NH:8][CH2:7][CH2:6]2.[N+:19]([C:22]1[CH:27]=[CH:26][C:25]([CH2:28][C:29]([O-])=[O:30])=[CH:24][CH:23]=1)([O-:21])=[O:20].O.ON1C2C=CC=CC=2N=N1.CCN=C=NCCCN(C)C.Cl.C(=O)([O-])O.[Na+]>CN(C=O)C.C(OCC)(=O)C>[CH3:1][O:2][C:3]1[C:4]([O:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH2:9][N:8]([C:29](=[O:30])[CH2:28][C:25]1[CH:24]=[CH:23][C:22]([N+:19]([O-:21])=[O:20])=[CH:27][CH:26]=1)[CH2:7][CH2:6]2参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
6-Methoxy-5-pentyloxy-1,2,3,4-tetrahydroisoquinoline (116 mg, 0.465 mmol), (4-nitrophenyl)acetate (101.1 mg, 0.558 mmol) and 1-hydroxybenzotriazol hydrate (81.7 mg, 0.605 mmol) were dissolved in DMF (2 ml), and WSC hydrochloride (125 mg, 0.651 mmol) was added to this solution under ice-cooling. After stirring at room temperature for 3 hours, ethyl acetate (3 ml) and saturated aqueous sodium hydrogencarbonate solution (3 ml) were added to the reaction mixture to separate the organic layer. The organic layer was dried over anhydrous sodium sulfate. The drying agent was filtered off and the filtrate was concentrated under reduced pressure to give a crude product of 1-(6-methoxy-5-pentyloxy-3,4-dihydro-1H-isoquinolin-2-yl)-2-(4-nitrophenyl)ethanone. This product was used for the next reaction.
後処理
- temperaturecooling
- customto separate the organic layer
- dry with materialThe organic layer was dried over anhydrous sodium sulfate
- filtrationThe drying agent was filtered off
- concentrationthe filtrate was concentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-da005e14829e466da540592819bcca09
- 出典データセット
- uspto-grants-2000_01
- 特許番号
- US06017919
関連ノート
読み込み中…