4-Bromobenzyl bromide → HCID 10691281, compound
Reaction equation
[N:1]1[CH:6]=[C:5]([NH:7][C:8]2[CH:13]=[CH:12][C:11]([C:14](=[O:16])[CH3:15])=[CH:10][CH:9]=2)[CH:4]=[N:3][CH:2]=1.[Br:17][C:18]1[CH:25]=[CH:24][C:21]([CH2:22]Br)=[CH:20][CH:19]=1>>[Br:17][C:18]1[CH:25]=[CH:24][C:21]([CH2:22][N:7]([C:8]2[CH:9]=[CH:10][C:11]([C:14](=[O:16])[CH3:15])=[CH:12][CH:13]=2)[C:5]2[CH:6]=[N:1][CH:2]=[N:3][CH:4]=2)=[CH:20][CH:19]=1Participants
3
Procedure
Starting compounds: 4'-[N-(pyrimidin-5-yl)amino]acetophenone and 4-bromobenzyl bromide
Sources & evidence
- ORD record
- ord-a54ab6c1c97d47b9ad2fca0136fb92ee
- Source dataset
- uspto-grants-1996_07
- Patent number
- US05538976
Reaction notes
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