Nitrate(1-), oxo- → HCID 66645094, compound

HRID 882839Notes

Reaction equation

HRID 882839 reaction equation
[CH2:1]([N:8]1[C@@H:12]([C:13]([OH:15])=O)[CH2:11][N:10]([CH3:16])[C:9]1=[O:17])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:18][CH:19]([CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)[CH:20]([OH:24])[C:21]([NH2:23])=[O:22].O[NH-].O=[N-]>>[NH2:23][C:21](=[O:22])[C:20](=[O:24])[CH:19]([NH:18][C:13]([C@H:12]1[CH2:11][N:10]([CH3:16])[C:9](=[O:17])[N:8]1[CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)=[O:15])[CH2:25][C:26]1[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=1

Participants

5

Reactant 4

HCID 3001380Nitrate(1-), oxo-HCID 138823553-Amino-2-hydroxy-4-phenylbutanamideHCID 66645156HCID 66645156, compoundHCID 178514248HCID 178514248, compound

Product 1

HCID 66645094HCID 66645094, compound

Procedure

Coupling of (R)-3-Benzyl-1-methyl-2-oxo-imidazolidine-4-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-e08012883cfa4f26a07e28ed26c27e8e
Source dataset
uspto-grants-2012_08
Patent number
US08236798B2

Reaction notes

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