反応式
[Br:1][C:2]1[C:11]2[CH2:10][CH2:9][CH2:8][CH:7]([NH2:12])[C:6]=2[CH:5]=[N:4][CH:3]=1.CCN(CC)CC.[C:20](Cl)(=[O:23])[CH2:21][CH3:22].O>C(Cl)Cl>[Br:1][C:2]1[C:11]2[CH2:10][CH2:9][CH2:8][CH:7]([NH:12][C:20](=[O:23])[CH2:21][CH3:22])[C:6]=2[CH:5]=[N:4][CH:3]=1参加物
6
実験手順
To a solution of (rac)-4-bromo-5,6,7,8-tetrahydro-isoquinolin-8-ylamine (intermediate A-2 [D]) (3.7 g, 16.3 mmol) and Et3N (3.3 g, 32.6 mmol) in DCM (50 mL) was added propionyl chloride (2.25 g, 24.4 mmol) at 0° C. The resulting reaction mixture was stirred for 3 hr before it was warmed up to room temperature and poured into water (50 mL) and extracted with DCM (2×50 mL). The combined organic layers were then dried over anhy. Na2SO4, filtered, and concentrated in vacuo. The residue was purified by silica gel column chromatography and afforded the title compound (4.29 g, 93% yield) as a white solid. MS: 283.0 (M+H+).
後処理
- customThe resulting reaction mixture
- extractionextracted with DCM (2×50 mL)
- customThe combined organic layers were then dried over anhy
- filtrationNa2SO4, filtered
- concentrationconcentrated in vacuo
- customThe residue was purified by silica gel column chromatography
出典と根拠
- ORDレコード
- ord-7bab575ed6c643dd9eeeca2ac76da0ae
- 出典データセット
- uspto-grants-2016_05
- 特許番号
- US09353081B2
関連ノート
読み込み中…