Benzyl 3-(2-(tert-butoxycarbonyl)benzyl)-4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decane-8-carboxylate → Tert-butyl 2-((4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoate
反応式
[C:1]([O:5][C:6]([C:8]1[CH:41]=[CH:40][CH:39]=[CH:38][C:9]=1[CH2:10][N:11]1[C:15](=[O:16])[C:14]2([CH2:21][CH2:20][N:19](C(OCC3C=CC=CC=3)=O)[CH2:18][CH2:17]2)[N:13]([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[CH2:12]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]>CO.[Pd]>[O:16]=[C:15]1[C:14]2([CH2:17][CH2:18][NH:19][CH2:20][CH2:21]2)[N:13]([C:32]2[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=2)[CH2:12][N:11]1[CH2:10][C:9]1[CH:38]=[CH:39][CH:40]=[CH:41][C:8]=1[C:6]([O:5][C:1]([CH3:4])([CH3:2])[CH3:3])=[O:7]参加物
4
実験手順
To a solution of benzyl 3-(2-(tert-butoxycarbonyl)benzyl)-4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decane-8-carboxylate (0.59 g, 1.06 mmol) in methanol (20 mL), was added 10 wt % palladium on carbon (0.1 g). After stirring under hydrogen at room temperature and atmospheric pressure for 2 hours, the reaction mixture was filtered, washed with methanol, concentrated in vacuo to obtain tert-butyl 2-((4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoate (0.4 g, 90%).
後処理
- filtrationthe reaction mixture was filtered
- washwashed with methanol
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-0754d1a0010c4fcaab8865161e717dec
- 出典データセット
- uspto-grants-2014_04
- 特許番号
- US08691836B2
反応ノート
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