Nitrate(1-), oxo- → (2R)-N-(4-Amino-3,4-dioxo-1-phenylbutan-2-yl)-5-oxo-1-[2-methoxy-6-(trifluoromethyl)benzyl]pyrrolidine-2-carboxamide
Reaction equation
[O:1]=[C:2]1[N:6]([CH2:7][C:8]2[C:13]([C:14]([F:17])([F:16])[F:15])=[CH:12][CH:11]=[CH:10][C:9]=2[O:18][CH3:19])[C@@H:5]([C:20]([OH:22])=O)[CH2:4][CH2:3]1.[NH2:23][CH:24]([CH2:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)[CH:25]([OH:29])[C:26]([NH2:28])=[O:27].O[NH-].O=[N-]>>[NH2:28][C:26](=[O:27])[C:25](=[O:29])[CH:24]([NH:23][C:20]([C@H:5]1[CH2:4][CH2:3][C:2](=[O:1])[N:6]1[CH2:7][C:8]1[C:13]([C:14]([F:17])([F:16])[F:15])=[CH:12][CH:11]=[CH:10][C:9]=1[O:18][CH3:19])=[O:22])[CH2:30][C:31]1[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=1Participants
5
Reactant 4
Product 1
Procedure
Coupling of (R)-5-oxo-1-(2-methoxy-6-trifluoromethyl-benzyl)-pyrrolidine-2-carboxylic acid with 3-amino-2-hydroxy-4-phenylbutanamide and oxidation of the resulting hydroxyamide intermediate to the corresponding ketoamide.
Sources & evidence
- ORD record
- ord-9a0d4ed61089434c95d71491ee9756da
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08236798B2
Reaction notes
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