5-methyl-1H-indole-4-carbonitrile → (5-methyl-1H-indol-4-yl)methanamine
反応式
[CH3:1][C:2]1[CH:10]=[CH:9][C:8]2[NH:7][CH:6]=[CH:5][C:4]=2[C:3]=1[C:11]#[N:12]>N.CO.[Ni]>[CH3:1][C:2]1[C:3]([CH2:11][NH2:12])=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[CH:5]2参加物
5
実験手順
A mixture of 302 (54 mg, 0.346 mmol) and Raney Ni (100 mg) in 7M ammonia in MeOH (20 mL) was stirred under hydrogen at RT for 3 h. It was filtered through Celite®, and the filtrate was concentrated under reduced pressure to afford 53 mg (95.7%) of (5-methyl-1H-indol-4-yl)methanamine (304) as yellow solid: MS (ESI) m/z=144.3 (M−16).
後処理
- filtrationIt was filtered through Celite®
- concentrationthe filtrate was concentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-7385944bd4a941fa9eef6221007e81fa
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08637537B2
反応ノート
読み込み中…