HCID 178450966, compound → HCID 178450965, compound
Reaction equation
[CH2:1]([O:5][CH:6]([O:37][CH2:38][CH2:39][CH2:40][CH3:41])[CH:7]([CH2:30][CH2:31][CH2:32][NH:33][C:34](=[NH:36])[NH2:35])[NH:8][C:9](=[O:29])[CH2:10][NH:11][C:12](=[O:28])[C@@H:13]([CH:25]([CH3:27])[CH3:26])[NH:14]C(OCC1C=CC=CC=1)=O)[CH2:2][CH2:3][CH3:4]>CO.[Pd]>[CH2:38]([O:37][CH:6]([O:5][CH2:1][CH2:2][CH2:3][CH3:4])[CH:7]([CH2:30][CH2:31][CH2:32][NH:33][C:34](=[NH:35])[NH2:36])[NH:8][C:9](=[O:29])[CH2:10][NH:11][C:12](=[O:28])[C@@H:13]([CH:25]([CH3:26])[CH3:27])[NH2:14])[CH2:39][CH2:40][CH3:41]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
132 mg of the N-benzyloxycarbonyl-D-valyl-glycyl-D,L-argininal dibutyl acetal was dissolved in 10 ml of methanol and subjected to catalytic reduction with palladium black for four hours. After the completion of the reaction, the palladium black was removed and the solvent was distilled off in vacuo to give 138 mg of D-valyl-glycyl-D,L-argininal dibutyl acetal in the form of a powder.
Workup
- customAfter the completion of the reaction
- customthe palladium black was removed
- distillationthe solvent was distilled off in vacuo
Sources & evidence
- ORD record
- ord-864692f12bcd4d56a1a34fed322eba3b
- Source dataset
- uspto-grants-1987_11
- Patent number
- US04708944
Reaction notes
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