Benzyl 1-methyl-oxindole-5-carboxylate → 2,3-Dihydro-1-methyl-2-oxo-1H-indole-5-carboxylic acid
反応式
[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][C:7]([C:11]([O:13]CC3C=CC=CC=3)=[O:12])=[CH:8][CH:9]=2)[CH2:4][C:3]1=[O:21]>C(OCC)(=O)C.CO.[Pd]>[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][C:7]([C:11]([OH:13])=[O:12])=[CH:8][CH:9]=2)[CH2:4][C:3]1=[O:21]参加物
5
実験手順
A solution of Example 59A (1.2 g, 4.27 mmol) in ethyl acetate (30 mL) and methanol (20 mL) was treated with 10% Pd/C (200 mg), stirred under hydrogen (balloon) for 18 hours, filtered through diatomaceous earth (Celite®) with 9:1 dichloromethane/methanol solution rinses, and concentrated to provide 460 mg of the desired product.
後処理
- filtrationfiltered through diatomaceous earth (Celite®) with 9:1 dichloromethane/methanol solution rinses
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-46869cd61e5d4451b0eb5d2da6041cd9
- 出典データセット
- uspto-grants-2001_05
- 特許番号
- US06228868B1
反応ノート
読み込み中…