反応式
[CH3:1][N:2](C)[C:3]1[CH:8]=[CH:7][C:6]([N+:9]([O-])=O)=[C:5]([N:12]2[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]2)[CH:4]=1.[CH3:19]O>[Pd]>[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][CH3:19])=[C:5]([N:12]2[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]2)[CH:4]=1参加物
4
実験手順
Using a procedure similar to Example 3, step (c), dimethyl-(4-nitro-3-piperidin-1-yl-phenyl)-amine (100 mg, 0.4 mmol, as prepared in the previous step) was stirred with 80 mg 5% Pd—C in 5 mL MeOH under H2 to afford 89 mg (100%) of the title compound as an oil, which was used immediately without further purification. Mass spectrum (ESI, m/z) calcd. for C13H21N3, 220.1 (M+H), found 220.1.
後処理
- customas prepared in the previous step)
出典と根拠
- ORDレコード
- ord-bd1616501d4f4ef8b89253b1c1924ab7
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07427683B2
関連ノート
読み込み中…