HCID 89800236, compound → HCID 89800333, compound
Reaction equation
C([O:8][C:9](=[O:32])[C@@H:10]1[CH2:14][CH2:13][CH2:12][N:11]1[C:15](=[O:31])[CH:16]([CH2:27][CH:28]([CH3:30])[CH3:29])[NH:17][C:18](=[O:26])[CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)C1C=CC=CC=1.[H][H]>CO.[C].[Pd]>[C:20]1([CH2:19][C:18]([NH:17][CH:16]([C:15]([N:11]2[CH2:12][CH2:13][CH2:14][C@H:10]2[C:9]([OH:32])=[O:8])=[O:31])[CH2:27][CH:28]([CH3:30])[CH3:29])=[O:26])[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
N-phenylacetyl-D,L-leucyl-L-proline benzyl ester (2 g) was dissolved in methanol (40 ml), and 10% palladium-carbon (200 mg) was added. The resulting mixture aerated with hydrogen was allowed to react at room temperature for 3 h, filtered and concentrated under reduced pressure to remove the solvent to give a colourless sticky matter (1.55 g, 98%), which was directly used for the next reaction.
Workup
- customto react at room temperature for 3 h
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customto remove the solvent
- customto give a colourless sticky matter (1.55 g, 98%), which
- customwas directly used for the next reaction
Sources & evidence
- ORD record
- ord-dc6887c10f434b009b85da277eb38fe3
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09434760B2
Reaction notes
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