Pyrrolidine → HCID 69890658, compound
Reaction equation
[CH2:1]([O:8][C:9]([NH:11][C@H:12]([C:24]([OH:26])=O)[CH2:13][CH2:14][CH2:15][NH:16][C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH:27]1[CH2:31][CH2:30][CH2:29][CH2:28]1>>[CH2:1]([O:8][C:9]([NH:11][C@H:12]([C:24](=[O:26])[N:27]1[CH2:31][CH2:30][CH2:29][CH2:28]1)[CH2:13][CH2:14][CH2:15][NH:16][C:17]([O:19][C:20]([CH3:21])([CH3:22])[CH3:23])=[O:18])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
Starting from (S)-N2-(benzyloxycarbonyl)-N5-(tert-butyloxycarbonyl)-ornithine and pyrrolidine, the expected product is obtained according to the procedure described in Step A of Example 3.
Sources & evidence
- ORD record
- ord-10418aaebe7248898a6a16e83500d028
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06716843B2
Reaction notes
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