Reaction equation
C([O:3][C:4](=[O:19])[CH:5]([N:7]1[CH2:12][CH2:11][CH2:10][CH:9]([NH:13][C:14]([O:16][CH3:17])=[O:15])[C:8]1=[O:18])[CH3:6])C.COC(N1CC(=O)N2C(C(OCC)=O)CCC2C1)=O>>[CH3:17][O:16][C:14]([NH:13][CH:9]1[CH2:10][CH2:11][CH2:12][N:7]([CH:5]([CH3:6])[C:4]([OH:19])=[O:3])[C:8]1=[O:18])=[O:15]Participants
3
Procedure
2-(3-Methoxycarbonylamino-2-oxo-piperidin-1-yl)-propionic acid was prepared by method 801 substituting 2-(3-methoxycarbonylamino-2-oxo-piperidin-1-yl)-propionic acid ethyl ester for 4-oxo-hexahydro-pyrrolo[1,2-a]pyrazine-2,6-dicarboxylic acid 6-ethyl ester 2-methyl ester. C10H16N2O5 calculated 244.1 observed [M+1]+ 245.1; rt=1.53 min.
Workup
- customrt=1.53 min.
Sources & evidence
- ORD record
- ord-969bde2042524a588fca7d1e8f6d3de3
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08822430B2
Linked notes
Loading…