HCID 54478759, compound → HCID 54339633, compound
Reaction equation
C([O:8][C:9](=[O:39])[C@H:10]([CH2:19][C:20]1[CH:25]=[CH:24][C:23]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=2[C:32]([O:34][C:35]([CH3:38])([CH3:37])[CH3:36])=[O:33])=[CH:22][CH:21]=1)[NH:11][C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])C1C=CC=CC=1>[Pd].C(O)C>[C:12]([NH:11][C@H:10]([C:9]([OH:39])=[O:8])[CH2:19][C:20]1[CH:25]=[CH:24][C:23]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=2[C:32]([O:34][C:35]([CH3:38])([CH3:37])[CH3:36])=[O:33])=[CH:22][CH:21]=1)([O:14][C:15]([CH3:17])([CH3:16])[CH3:18])=[O:13]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of N-Boc-para-(2'-t butoxycarbonylphenyl)phenylalanine-benzyl ester and 10% Palladium on charcoal (0.030 g) in ethanol 20 mL was hydrogenated at 35 psi for 23.5 hours. The reaction mixture was filtered through celite and evaporated to dryness to give the N-Boc-para-(2'-t butoxycarbonylphenyl)phenylalanine (0.175 g).
Workup
- filtrationThe reaction mixture was filtered through celite
- customevaporated to dryness
Sources & evidence
- ORD record
- ord-e4bc45d9f4764564b71c8a97cedec5eb
- Source dataset
- uspto-grants-2000_06
- Patent number
- US06071707
Reaction notes
Loading…