3-[4-(3-Benzyloxyphenyl)-2-oxo-pyrrolidin-1-yl]benzamide → 3-[4-(3-Hydroxyphenyl)-2-oxo-pyrrolidin-1-yl]benzamide
反応式
C([O:8][C:9]1[CH:10]=[C:11]([CH:15]2[CH2:19][N:18]([C:20]3[CH:21]=[C:22]([CH:26]=[CH:27][CH:28]=3)[C:23]([NH2:25])=[O:24])[C:17](=[O:29])[CH2:16]2)[CH:12]=[CH:13][CH:14]=1)C1C=CC=CC=1>CCO.[Pd]>[OH:8][C:9]1[CH:10]=[C:11]([CH:15]2[CH2:19][N:18]([C:20]3[CH:21]=[C:22]([CH:26]=[CH:27][CH:28]=3)[C:23]([NH2:25])=[O:24])[C:17](=[O:29])[CH2:16]2)[CH:12]=[CH:13][CH:14]=1参加物
4
実験手順
To a solution of 3-[4-(3-benzyloxyphenyl)-2-oxo-pyrrolidin-1-yl]benzamide (1.2 g) in 50 mL EtOH was added 10% Pd/C (100 mg). The resulting mixture was stirred under H2 for 4 h, filtered, and concentrated under reduced pressure to give 0.8 g of crude product.
後処理
- filtrationfiltered
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-0976ff6980f54565b1123cfec164a133
- 出典データセット
- uspto-grants-2009_02
- 特許番号
- US07495016B2
反応ノート
読み込み中…