4-Chlorobenzylamine → HCID 136381095, compound
Reaction equation
[CH3:1][C:2]([O:5][C:6]([NH:8][C@@H:9]([C:20]([OH:22])=O)[CH2:10][CH2:11][CH2:12][N:13]=[C:14]([NH:16][N+:17]([O-:19])=[O:18])[NH2:15])=[O:7])([CH3:4])[CH3:3].[Cl:23][C:24]1[CH:29]=[CH:28][C:27]([CH2:30][NH2:31])=[CH:26][CH:25]=1.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F>>[Cl:23][C:24]1[CH:29]=[CH:28][C:27]([CH2:30][NH:31][C:20](=[O:22])[C@@H:9]([CH2:10][CH2:11][CH2:12][NH:13][C:14]([NH2:15])=[N:16][N+:17]([O-:19])=[O:18])[NH:8][C:6]([O:5][C:2]([CH3:1])([CH3:3])[CH3:4])=[O:7])=[CH:26][CH:25]=1Participants
4
Procedure
Prepared analogously to Example 5d) from Boc-D-Arg (NO2)-OH, (4-chlorophenyl) methylamine and TBTU in a yield of 87% of theory.
Sources & evidence
- ORD record
- ord-db9262c8186e4a15876f0f001703f7da
- Source dataset
- uspto-grants-1997_04
- Patent number
- US05616620
Reaction notes
Loading…