Benzylamine → HCID 178454202, compound
Reaction equation
[CH2:1]([NH2:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH:9]([C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[C@H:10]([C:22](O)=[O:23])[CH2:11][CH2:12][CH2:13][NH:14][C:15](=[NH:21])[N:16]([OH:20])[N+:17]([O-:19])=[O:18]>>[NH:9]([C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[C@H:10]([C:22]([NH:8][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)=[O:23])[CH2:11][CH2:12][CH2:13][NH:14][C:15](=[NH:21])[N:16]([OH:20])[N+:17]([O-:19])=[O:18]Participants
3
Procedure
Boc-Arg(NO2)(OH)CONHBn was prepared according to Example 42 by coupling benzylamine to Boc-Arg(NO2)(OH)COOH in a 81% yield.
Sources & evidence
- ORD record
- ord-38c97ee4f0454656ae2617960d98313c
- Source dataset
- uspto-grants-2001_06
- Patent number
- US06245743B1
Reaction notes
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