5-ethyl-6-nitro-1H-indole → 5-ethyl-1H-indol-6-ylamine
反応式
[CH2:1]([C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[N+:12]([O-])=O)[NH:8][CH:7]=[CH:6]2)[CH3:2]>[Ni]>[CH2:1]([C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[NH2:12])[NH:8][CH:7]=[CH:6]2)[CH3:2]参加物
3
実験手順
A suspension of 5-ethyl-6-nitro-1H-indole (1.9 g, 10 mmol) and Raney Nickel (1 g) was hydrogenated under H2 (1 atm) at room temperature for 2 h. The catalyst was filtered off and the filtrate was concentrated to dryness. The residue was purified by silica gel column to give 5-ethyl-1H-indol-6-amine (760 mg, 48% over two steps). 1H NMR (CDCl3) δ 7.90 (br s, 1H), 7.41 (s, 1H), 7.00 (s, 1H), 6.78 (s, 2H), 6.39 (s, 1H), 3.39 (br s, 2H), 2.63 (q, J=7.2 Hz, 2H), 1.29 (t, J=6.9 Hz, 3H); MS (ESI) m/e (M+H+) 161.1.
後処理
- filtrationThe catalyst was filtered off
- concentrationthe filtrate was concentrated to dryness
- customThe residue was purified by silica gel column
出典と根拠
- ORDレコード
- ord-067e62b72daf443f809f349d63b20a19
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08623905B2
反応ノート
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