Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356650Generated: November 1, 2026

2-Bromobenzyl bromide → 3-Bromo-4-[3-(4-cyano-3-trifluoromethylphenyl)-5,5-dimethyl-2,4-dioxoimidazolidin-1-ylmethyl]-N,N-dimethylbenzenesulfonamide

https://huagongshe.com/reaction/2356650

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromobenzyl bromideHCID 76965—
Reactant4-(4,4-Dimethyl-2,5-dioxoimidazolidin-1-yl)-2-trifluoromethylbenzonitrileHCID 11162285—
Reactant3-bromo-4-bromomethyl-N,N-dimethylbenzenesulfonamideHCID 68678156—
Product3-Bromo-4-[3-(4-cyano-3-trifluoromethylphenyl)-5,5-dimethyl-2,4-dioxoimidazolidin-1-ylmethyl]-N,N-dimethylbenzenesulfonamideHCID 68677107—

Reaction Steps

Compound 146.2 was prepared as described for example 1.2, by reacting compound 1.1, instead of with 2-bromobenzyl bromide, with 3-bromo-4-bromomethyl-N,N-dimethylbenzenesulfonamide (146.3, prepared by reacting 3-bromo-4,N,N-trimethylbenzenesulfonamide with N-bromosuccinimide and N,N′-azobis(2-methylpropionitrile) in tetrachloromethane). 3-Bromo-4-[3-(4-cyano-3-trifluoromethylphenyl)-5,5-dimethyl-2,4-dioxoimidazolidin-1-ylmethyl]-N,N-dimethylbenzenesulfonamide was obtained. (Molecular weight 572.03 (C22H20BrF3N4O4S); retention time Rt=2.38 min. [B]; MS (ESI): 573.25 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759366B2
Source datasetuspto-grants-2010_07
ORD IDord-b48e30df14314521a80ac652292aa868
Source noteuspto-grants-2010_07