Diethyl Malonate → HCID 178468432, compound
Reaction equation
[CH2:1]([N:8]1[CH2:14][CH2:13][C:12]([CH:15]=[N:16][OH:17])=[C:11](Cl)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:19](OCC)(=[O:26])[CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22].[H-].[Na+]>[Cu]Br>[CH2:24]([O:23][C:21]([C:20]1[C:11]2[CH2:10][CH2:9][N:8]([CH2:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[CH2:14][CH2:13][C:12]=2[CH:15]=[N+:16]([O-:17])[C:19]=1[OH:26])=[O:22])[CH3:25]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared from 1-benzyl-4-chloro-5-hydroxyiminomethyl-2,3,6,7-tetrahydro-1H-azepine by reaction with diethyl malonate in the presence of sodium hydride and catalytic amounts of copper(I) bromide at 100° C.
Sources & evidence
- ORD record
- ord-8427a90930f54a9caddc457a71ade9aa
- Source dataset
- uspto-grants-1998_10
- Patent number
- US05827849
Reaction notes
Loading…