HCID 131713851, compound → HCID 131713850, compound
Reaction equation
[NH:1](C(OCC1C=CC=CC=1)=O)[C@H:2]([C:7]([N:9]1[CH2:33][CH2:32][CH2:31][C@H:10]1[C:11]([NH:13][C@H:14]([C:20]([NH:22][NH:23][C:24]([O:26][C:27]([CH3:30])([CH3:29])[CH3:28])=[O:25])=[O:21])[CH2:15][CH2:16][C:17](=[O:19])[NH2:18])=[O:12])=[O:8])[CH2:3][CH:4]([CH3:6])[CH3:5]>CO.[Pd]>[NH2:1][C@H:2]([C:7]([N:9]1[CH2:33][CH2:32][CH2:31][C@H:10]1[C:11]([NH:13][C@H:14]([C:20]([NH:22][NH:23][C:24]([O:26][C:27]([CH3:29])([CH3:28])[CH3:30])=[O:25])=[O:21])[CH2:15][CH2:16][C:17](=[O:19])[NH2:18])=[O:12])=[O:8])[CH2:3][CH:4]([CH3:6])[CH3:5]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
3.50 Grams of Z-Leu-Pro-Gln-NHNHBoc was dissolved in 50 ml of methanol and was catalytically reduced by using palladium as the catalyst to obtain H-Leu-Pro-Gln-NHNHBoc.
Sources & evidence
- ORD record
- ord-6231a747b26540bdb6a2148d5cd9334e
- Source dataset
- uspto-grants-1984_10
- Patent number
- US04474754
Reaction notes
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