Ammonia methanol → (3S)-3-phenylcyclopentanamine
反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([C@H:8]2[CH2:12][CH2:11][C:10](=[N:13]O)[CH2:9]2)=[CH:4][CH:3]=1.N.CO>[Ni].O>[C:5]1([C@H:8]2[CH2:12][CH2:11][CH:10]([NH2:13])[CH2:9]2)[CH:6]=[CH:7][CH:2]=[CH:3][CH:4]=1参加物
5
実験手順
A solution of Example 1C (10 g, 39.4 mmol) and 7M NH3/MeOH (100 mL) was added to Ra—Ni 2800, water slurry (40.0 g, 682 mmol) in a 50 mL pressure bottle. The mixture was stirred at room temperature for 32 hours at 30 psi. HPLC indicated complete reaction. The mixture was filtered through a nylon membrane, concentrated, and diluted with MTBE (300 mL) and 2N NaOH (150 mL). The layers were separated and the organic layer was washed with water (100 mL) and brine (50 mL), dried (Na2SO4), filtered, and concentrated to afford the title compound (5.86 g, 36.3 mmol, 92%). MS (LCMS) m/z 162 (M+H)+.
後処理
- customreaction
- filtrationThe mixture was filtered through a nylon membrane
- concentrationconcentrated
- additiondiluted with MTBE (300 mL) and 2N NaOH (150 mL)
- customThe layers were separated
- washthe organic layer was washed with water (100 mL) and brine (50 mL)
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-74c3611d2f2d4331b2f13943537956e8
- 出典データセット
- uspto-grants-2014_08
- 特許番号
- US08802711B2
反応ノート
読み込み中…