4-Nitrobenzyl bromide → 5-[N-(4-Nitrobenzyl)-N-(4-nitrophenyl)amino]pyrimidine
Reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:10][C:11]2[CH:12]=[N:13][CH:14]=[N:15][CH:16]=2)=[CH:6][CH:5]=1)([O-:3])=[O:2].[N+:17]([C:20]1[CH:27]=[CH:26][C:23]([CH2:24]Br)=[CH:22][CH:21]=1)([O-:19])=[O:18]>>[N+:17]([C:20]1[CH:27]=[CH:26][C:23]([CH2:24][N:10]([C:11]2[CH:16]=[N:15][CH:14]=[N:13][CH:12]=2)[C:7]2[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:9][CH:8]=2)=[CH:22][CH:21]=1)([O-:19])=[O:18]Participants
3
Procedure
Starting compounds: 5-[(4-nitrophenyl)amino]pyrimidine and 4-nitrobenzyl bromide
Sources & evidence
- ORD record
- ord-ae43187a914245039976d4ec00c1a970
- Source dataset
- uspto-grants-1996_07
- Patent number
- US05538976
Reaction notes
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