反応式
[Br:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5](Cl)=[N:4][CH:3]=1.CO.[CH2:15]([NH2:17])[CH3:16]>>[Br:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([NH:17][CH2:15][CH3:16])=[N:4][CH:3]=1参加物
4
反応条件
- 温度
- 50 °C
実験手順
To a suspension of 4-bromo-1 chloroisoquinoline (0.831 g, 3.43 mmol) in MeOH (10.3 mL, 254 mmol) was added ethylamine (70% in water, 1.1 mL). The mixture was heated at 50° C. for 16 h. The mixture was concentrated. The residue was partitioned between water (20 mL) and DCM (20 mL). DCM layer was separated. The aqueous layer was extracted with DCM (10 mL) The combined DCM solutions were dried (Na2SO4). Filtration and concentration gave 4-bromo-N-ethylisoquinolin-1-amine (0.761 g, 88%). LCMS: M+H+=251.
後処理
- concentrationThe mixture was concentrated
- customThe residue was partitioned between water (20 mL) and DCM (20 mL)
- customDCM layer was separated
- extractionThe aqueous layer was extracted with DCM (10 mL) The combined DCM solutions
- dry with materialwere dried (Na2SO4)
- filtrationFiltration and concentration
出典と根拠
- ORDレコード
- ord-ac312d68479d428696847172550e0583
- 出典データセット
- uspto-grants-2012_05
- 特許番号
- US08173650B2
関連ノート
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