(S)-3-(Benzyl((S)-1-phenylethyl)amino)heptan-1-ol → (S)-3-aminoheptan-1-ol
Reaction equation
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]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
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.
Workup
- filtrationThe reaction mixture was filtered
- customthe solvent evaporated
Sources & evidence
- ORD record
- ord-58baea65f88c45b4bd5a90fa37910cab
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765939B2
Reaction notes
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