2-Bromo-5-bromomethylpyridine → 5-[N-[(2-Bromopyridin-5-yl)methyl]-N-(4cyanophenyl)amino]pyrimidine
Reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([NH:9][C:10]2[CH:11]=[N:12][CH:13]=[N:14][CH:15]=2)=[CH:5][CH:4]=1)#[N:2].[Br:16][C:17]1[CH:22]=[CH:21][C:20]([CH2:23]Br)=[CH:19][N:18]=1>>[Br:16][C:17]1[CH:22]=[CH:21][C:20]([CH2:23][N:9]([C:10]2[CH:15]=[N:14][CH:13]=[N:12][CH:11]=2)[C:6]2[CH:7]=[CH:8][C:3]([C:1]#[N:2])=[CH:4][CH:5]=2)=[CH:19][N:18]=1Participants
3
Procedure
Starting compounds: 5-[(4-Cyanophenyl) amino]pyrimidine and 2-bromo-5-(bromomethyl)pyridine
Sources & evidence
- ORD record
- ord-3b22dc50aa6145e9a75b09c3cbf97b2c
- Source dataset
- uspto-grants-1996_07
- Patent number
- US05538976
Reaction notes
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