Dimethyl Sulfide → HCID 59772401、化合物
反応式
[Br:1][C:2]1[CH:18]=[CH:17][CH:16]=[CH:15][C:3]=1[CH2:4][O:5][C:6]1[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][C:7]=1[C:8]#[N:9].CSC>ClCCCl>[Br:1][C:2]1[CH:18]=[CH:17][CH:16]=[CH:15][C:3]=1[CH2:4][O:5][C:6]1[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][C:7]=1[CH2:8][NH2:9]参加物
反応条件
- 温度
- 65 °C
実験手順
To a stirred solution of 2-(2-Bromo-benzyloxy)-5-chloro-benzonitrile Example 348A (1.52 g, 4.71 mmol) in DCE (50 mL) under argon was added BH3 DMS (30.0 mL, 18.8 mmol). The reaction mixture was heated at 65° C. for 14 h and then cooled to room temperature. The mixture was quenched with 1N HCl solution slowly (25 mL). This solution was then mixed with 1N NaOH solution (30 mL), and extracted with EtOAc (3×80 mL). The combined EtOAc extracts were washed with saturated NaHCO3 solution (1×40 mL) and brine (1×40 mL). The organic layer was dried (MgSO4), filtered and concentrated in vacuo to give 0.92 g (60%) of crude 2-(2-Bromo-benzyloxy)-5-chloro-benzylamine Example 348B which was used as is without further purification. HPLC Rt=2.87 min (YMC S5 ODS column 4.6×50 mm, 10-90% aqueous methanol over 4 minutes containing 0.2% phosphoric acid, 4 mL/min, monitoring at 220 nm) LC/MS: M+H=326
後処理
- temperaturecooled to room temperature
- customThe mixture was quenched with 1N HCl solution slowly (25 mL)
- additionThis solution was then mixed with 1N NaOH solution (30 mL)
- extractionextracted with EtOAc (3×80 mL)
- washThe combined EtOAc extracts were washed with saturated NaHCO3 solution (1×40 mL) and brine (1×40 mL)
- dry with materialThe organic layer was dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-de831421b86341ccae5bd017d3ffeba7
- 出典データセット
- uspto-grants-2008_08
- 特許番号
- US07417040B2
反応ノート
読み込み中…