HCID 22570297、化合物 → Methyl 3-(5-hydroxyindolyl)-2-methylpropanoate
反応式
[CH3:1][CH:2]([CH2:7][C:8]1[NH:9][C:10]2[C:15]([CH:16]=1)=[CH:14][C:13]([O:17]CC1C=CC=CC=1)=[CH:12][CH:11]=2)[C:3]([O:5][CH3:6])=[O:4]>C(O)C.[Pd]>[OH:17][C:13]1[CH:14]=[C:15]2[C:10](=[CH:11][CH:12]=1)[NH:9][C:8]([CH2:7][CH:2]([CH3:1])[C:3]([O:5][CH3:6])=[O:4])=[CH:16]2参加物
4
実験手順
A mixture of methyl 2-methyl-3-[5-benzyloxyindolyl]propanoate (0.18 g, 0.56 mmol), as prepared in the preceding step, 10% palladium(0) on carbon (0.018 g) in ethanol (10 mL) was stirred at ambient temperature under hydrogen (balloon) overnight (16 h). The catalyst was removed by filtration through Celite. The filtrate was concentrated to give the title compound as a light brown oil (0.11 g, 85%) which was used directly in the next reaction.
後処理
- customThe catalyst was removed by filtration through Celite
- concentrationThe filtrate was concentrated
出典と根拠
- ORDレコード
- ord-5053926935a34cf8afad0bbb8c7dee8e
- 出典データセット
- uspto-grants-2007_07
- 特許番号
- US07241789B2
反応ノート
読み込み中…