1-Pyrrolidineacetic acid, 4-hydroxy-2-oxo-, (+-)- → HCID 20163741, compound
Reaction equation
[OH:1][CH:2]1[CH2:6][N:5]([CH2:7][C:8]([OH:10])=O)[C:4](=[O:11])[CH2:3]1.[CH3:12][C:13]1([CH3:19])[NH:17][C:16](=[O:18])[CH2:15][NH:14]1>>[CH3:12][C:13]1([CH3:19])[NH:17][C:16](=[O:18])[CH2:15][N:14]1[C:8](=[O:10])[CH2:7][N:5]1[CH2:6][CH:2]([OH:1])[CH2:3][C:4]1=[O:11]Participants
3
Procedure
The same procedure of Example 10, starting from 4-hydroxy-2-oxo-1-pyrrolidineacetic acid and 2,2-dimethyl-4-imidazolidinone, afforded the title compound, m.p. 250° C. (dec).
Sources & evidence
- ORD record
- ord-e298c2b6726c40029f7f3a0c9c634bce
- Source dataset
- uspto-grants-1987_10
- Patent number
- US04703054
Reaction notes
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