(S)-3-(Benzyl((S)-1-phenylethyl)amino)heptan-1-ol → (S)-3-aminoheptan-1-ol
反応式
C([N:8]([C@H](C1C=CC=CC=1)C)[C@@H:9]([CH2:13][CH2:14][CH2:15][CH3:16])[CH2:10][CH2:11][OH:12])C1C=CC=CC=1>CCO.[Pd]>[NH2:8][C@@H:9]([CH2:13][CH2:14][CH2:15][CH3:16])[CH2:10][CH2:11][OH:12]参加物
4
実験手順
A solution of the product from step (iv) (5 g) and 5% Pd/C (0.5 g) in EtOH (25 mL) was hydrogenated under 5 bar at rt for 5 days. A further portion of 5% Pd/C (1.5 g) was added, and the reaction mixture hydrogenated under 5 bar at rt for a further 1 day. The reaction mixture was filtered and the solvent evaporated to give the subtitle compound 1.8 g.
後処理
- filtrationThe reaction mixture was filtered
- customthe solvent evaporated
出典と根拠
- ORDレコード
- ord-bfa52c3e9e8c42bd8f27ad6e6f30621d
- 出典データセット
- uspto-grants-2012_09
- 特許番号
- US08268990B2
反応ノート
読み込み中…