Methyl (4-nitro-1-imidazolyl)acetate → (4-[2-[2-(3,5-Difluoro-phenyl)-acetylamino]-pentanoylamino]-imidazol-1-yl)-acetic acid methyl ester
Reaction equation
[CH3:1][O:2][C:3](=[O:13])[CH2:4][N:5]1[CH:9]=[C:8]([N+:10]([O-])=O)[N:7]=[CH:6]1.[F:14][C:15]1[CH:16]=[C:17]([CH2:22][C:23]([NH:25][CH:26]([CH2:30][CH2:31][CH3:32])[C:27](O)=[O:28])=[O:24])[CH:18]=[C:19]([F:21])[CH:20]=1>>[CH3:1][O:2][C:3](=[O:13])[CH2:4][N:5]1[CH:9]=[C:8]([NH:10][C:27](=[O:28])[CH:26]([NH:25][C:23](=[O:24])[CH2:22][C:17]2[CH:18]=[C:19]([F:21])[CH:20]=[C:15]([F:14])[CH:16]=2)[CH2:30][CH2:31][CH3:32])[N:7]=[CH:6]1Participants
3
Procedure
(4-Nitro-imidazol-1-yl)-acetic acid methyl ester was reduced and coupled with 2-[2-(3,5-Difluoro-phenyl)-acetylamino]-pentanoic acid to afford the title compound; MS 409.1 m/z (M+1).
Sources & evidence
- ORD record
- ord-2bb27ef17cb840fcaa3c1c412d5cd450
- Source dataset
- uspto-grants-2010_08
- Patent number
- US07781435B2
Reaction notes
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