tert-Butyl (4-(furan-3-yl)-2-nitrophenyl)carbamate → (2-Amino-4-furan-3-yl-phenyl)-carbamic acid tert.-butyl ester
反応式
[C:1]([O:5][C:6](=[O:22])[NH:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]2[CH:18]=[CH:17][O:16][CH:15]=2)=[CH:10][C:9]=1[N+:19]([O-])=O)([CH3:4])([CH3:3])[CH3:2]>[Ni]>[C:1]([O:5][C:6](=[O:22])[NH:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]2[CH:18]=[CH:17][O:16][CH:15]=2)=[CH:10][C:9]=1[NH2:19])([CH3:4])([CH3:2])[CH3:3]参加物
3
実験手順
Prepared from (4-furan-3-yl-2-nitrophenyl)-carbamic acid tert.-butyl ester (Example B6) by catalytic hydrogenation with Raney-Ni according to the general procedure G (method a). Obtained as a light brown solid. (744 mg).
後処理
- customObtained as a light brown solid
出典と根拠
- ORDレコード
- ord-ca6ed3d5cb884179b2474a6b91b9791b
- 出典データセット
- uspto-grants-2003_01
- 特許番号
- US06509328B1
反応ノート
読み込み中…