Allyl bromide → HCID 19863363, compound
Reaction equation
[CH2:1]([N:3]([CH2:16][CH2:17][CH2:18][CH2:19][CH:20]([CH3:22])[CH3:21])[CH2:4][CH2:5][NH:6][C:7]1[CH:12]=[CH:11][C:10]([N+:13]([O-:15])=[O:14])=[CH:9][CH:8]=1)[CH3:2].[CH2:23](Br)[CH:24]=[CH2:25]>>[CH2:1]([N:3]([CH2:16][CH2:17][CH2:18][CH2:19][CH:20]([CH3:21])[CH3:22])[CH2:4][CH2:5][N:6]([C:7]1[CH:12]=[CH:11][C:10]([N+:13]([O-:15])=[O:14])=[CH:9][CH:8]=1)[CH2:25][CH:24]=[CH2:23])[CH3:2]Participants
3
Procedure
In a manner similar to Preparation 12 react N-Ethyl-N-(5-methylhexyl)-N'-(4-nitrophenyl)-1,2-ethanediamine with allyl bromide to provide the title compound.
Workup
- customIn a manner similar to Preparation 12
Sources & evidence
- ORD record
- ord-d4bc62cc2b43489d84d929a3da7f008f
- Source dataset
- uspto-grants-1990_03
- Patent number
- US04906634
Reaction notes
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