反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][N:10]=1)[C:6]#[N:7].N>CO.[Ni]>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:6][NH2:7])[CH:8]=[CH:9][N:10]=1参加物
5
実験手順
To the solution of 2-methoxyisonicotinonitrile 56-1 (1.1 g, 8.2 mmol) in methanol with 7 N NH3 was added Raney-Nickel (1.0 g). The reaction was shaken under H2 at 50 psi at room temperature in Parr shaker for 12 hours. The Raney-Nickel was removed by rotary evaporation and the filtrate was taken to dryness by rotary evaporation to give crude (2-methoxypyridin-4-yl)methanamine 56-2. MS m/z 139.2 (M+1).
後処理
- customThe Raney-Nickel was removed by rotary evaporation
- customthe filtrate was taken to dryness by rotary evaporation
出典と根拠
- ORDレコード
- ord-789e41ddbe0f464da7f794949dfd6c7c
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09181235B2
関連ノート
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