反応式
[N+:1]([CH2:4][C:5]12[CH2:12][CH2:11][CH2:10][N:9]1[CH2:8][CH2:7][CH2:6]2)([O-])=O>[Ni].C(O)C>[NH2:1][CH2:4][C:5]12[CH2:12][CH2:11][CH2:10][N:9]1[CH2:8][CH2:7][CH2:6]2参加物
4
反応条件
- 温度
- 20 °C
実験手順
To a suspension of Raney nickel (300 mg) in 5.0 ml of ethanol, 7a-nitromethyl-2,3,5,6,7,7a-hexahydro-1H-pyrrolizine (300 mg, 1.76 mmol, obtained in Example 1) was added and the resulting mixture was stirred for 1 hour at 20° C. under hydrogen atmosphere. The catalyst was filtered off, the filtrate was concentrated, and the resulting crude product was distilled in vacuo to afford 185 mg of the desired compound (Yield: 75%).
後処理
- additionwas added
- filtrationThe catalyst was filtered off
- concentrationthe filtrate was concentrated
- distillationthe resulting crude product was distilled in vacuo
出典と根拠
- ORDレコード
- ord-78612acd1ee047b1a1d64e394c2e893f
- 出典データセット
- uspto-grants-1991_01
- 特許番号
- US04985569
関連ノート
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