Glycinamide → N-(2-Amino-2-oxoethyl)-2-(4-hydroxy-2-oxopyrrolidin-1-yl)acetamide
Reaction equation
[OH:1][CH:2]1[CH2:6][N:5]([CH2:7][C:8]([O:10]CC)=O)[C:4](=[O:13])[CH2:3]1.[NH2:14][CH2:15][C:16]([NH2:18])=[O:17]>>[OH:1][CH:2]1[CH2:6][N:5]([CH2:7][C:8]([NH:14][CH2:15][C:16]([NH2:18])=[O:17])=[O:10])[C:4](=[O:13])[CH2:3]1Participants
3
Conditions
- Temperature
- 80 °C
Procedure
A mixture of ethyl 4-hydroxy-2-oxo-1-pyrrolidineacetate (0.5 g) and glycinamide (0.6 g) was stirred under nitrogen at 80° C. for 4 hours. After cooling, the mixture was chromatographed on a silica gel column, by eluting with dichloromethane/methanol 7:3, affording the title compound (250 mg).
Workup
- temperatureAfter cooling
- customthe mixture was chromatographed on a silica gel column
- washby eluting with dichloromethane/methanol 7:3
Sources & evidence
- ORD record
- ord-7fc5fbd3df30416bb7ab1159c463d1e1
- Source dataset
- uspto-grants-1989_09
- Patent number
- US04868313
Reaction notes
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