Diethylphosphite → HCID 19084794, compound
Reaction equation
[O:1]=[C:2]([CH2:8][CH2:9][NH:10][C:11]1[CH:12]=[N:13][CH:14]=[CH:15][CH:16]=1)[C:3]([O:5][CH2:6][CH3:7])=[O:4].[P:17]([O-:24])([O:21][CH2:22][CH3:23])[O:18][CH2:19][CH3:20]>>[CH2:19]([O:18][P:17]([O:21][CH2:22][CH3:23])([C:2]([OH:1])([CH2:8][CH2:9][NH:10][C:11]1[CH:12]=[N:13][CH:14]=[CH:15][CH:16]=1)[C:3]([O:5][CH2:6][CH3:7])=[O:4])=[O:24])[CH3:20]Participants
3
Procedure
A mixture of 3.36 g (0.01 mole) of ethyl 2-oxo-4-(3-pyridylamino)butanoate in 6.9 g (0.05 mole) of diethyl phosphite is stirred at 20°-30° for 4 days. The excess diethyl phosphite is removed under vacuum on a rotary evaporator, and the crude product is purified by flash chromatography on silica gel using chloroform/ethanol as eluant.
Workup
- customThe excess diethyl phosphite is removed under vacuum on a rotary evaporator
- customthe crude product is purified by flash chromatography on silica gel
Sources & evidence
- ORD record
- ord-5b46e13d85dc4933b57d69b9f0637894
- Source dataset
- uspto-grants-1998_06
- Patent number
- US05760021
Reaction notes
Loading…