Methanol → 3-Amino-3-cyclohexyl-N-(3,3-dimethyl-butyl)-propionamide
反応式
C([N:8](C(C1C=CC=CC=1)C)[CH:9]([CH:20]1[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1)[CH2:10][C:11]([NH:13][CH2:14][CH2:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:12])C1C=CC=CC=1.CO.[H][H]>C(OCC)(=O)C.C(O)C.[Pd]>[NH2:8][CH:9]([CH:20]1[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25]1)[CH2:10][C:11]([NH:13][CH2:14][CH2:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:12]参加物
7
実験手順
In a Parr bottle 10% Pd/C (0.8 g) was cooled to −78° C., followed by addition of a solution of 3-[benzyl-(1-phenyl-ethyl)-amino]-3-cyclohexyl-N-(3,3-dimethyl-butyl)-propionamide (0.8 g, 1.78 mmol) in ethyl acetate (10 mL), ethanol (100 mL), and methanol (20 mL). The resulting mixture was subjected to hydrogen atmosphere and shaken for 3 h. The hydrogen was purged with nitrogen, the reaction mixture was filtered (glass fiber filter paper) and the solvent was evaporated under reduced pressure to yield a residue.
後処理
- customThe hydrogen was purged with nitrogen
- filtrationthe reaction mixture was filtered
- filtration(glass fiber filter paper)
- customthe solvent was evaporated under reduced pressure
- customto yield a residue
出典と根拠
- ORDレコード
- ord-e0a7adef03514bba81d8abdcb9d16fbf
- 出典データセット
- uspto-grants-2009_05
- 特許番号
- US07531545B2
反応ノート
読み込み中…