4-Bromobenzyl bromide → HCID 10788147, compound

HRID 1735767Notes

Reaction equation

HRID 1735767 reaction equation
[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]2[CH:13]=[N:14][CH:15]=[N:16][CH:17]=2)=[CH:7][CH:6]=1)(=[O:4])=[O:3].[Br:18][C:19]1[CH:26]=[CH:25][C:22]([CH2:23]Br)=[CH:21][CH:20]=1>>[Br:18][C:19]1[CH:26]=[CH:25][C:22]([CH2:23][N:11]([C:12]2[CH:17]=[N:16][CH:15]=[N:14][CH:13]=2)[C:8]2[CH:7]=[CH:6][C:5]([S:2]([CH3:1])(=[O:3])=[O:4])=[CH:10][CH:9]=2)=[CH:21][CH:20]=1

Participants

3

Reactant 2

HCID 685274-Bromobenzyl bromideHCID 10634349HCID 10634349, compound

Product 1

HCID 10788147HCID 10788147, compound

Procedure

Starting compounds: 5-[N-(4-methylsulfonylphenyl)amino]pyrimidine and 4-bromobenzyl bromide

Sources & evidence

ORD record
ord-3e9c4195afc847f6ab8bf6ed56774f77
Source dataset
uspto-grants-1996_07
Patent number
US05538976

Reaction notes

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