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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665002Generated: October 25, 2026

Diisopropylethylamine → N-(5-bromo-thiophen-2-ylmethyl)-2-trifluoromethyl-benzenesulfonamide

https://huagongshe.com/reaction/1665002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Trifluoromethylbenzenesulphonyl chlorideHCID 136616—
Reactant(5-Bromothiophen-2-yl)methanamineHCID 23130577—
SolventDichloromethaneHCID 6344—
ProductN-(5-bromo-thiophen-2-ylmethyl)-2-trifluoromethyl-benzenesulfonamideHCID 3540889757.2%

Reaction Steps

To a stirred suspension of 1-(5-bromo-2-thienyl)-methanamine (0.5 g) in dichloromethane (8 mL) were added 2-(trifluoromethyl)-benzenesulfonyl chloride (0.67 g) and N-ethyl-diisopropylamine (0.37 g) at 0° C. After stirring for 10 min, the ice bath was removed and the mixture was stirred for 40 min. The reaction mixture was diluted with dichloromethane and washed with 0.5 M HCl and with water. The organic phase was dried (MgSO4), filtered and concentrated. The residue was suspended in cyclohexane. The solid was collected by filtration and dried to give N-(5-bromo-thiophen-2-ylmethyl)-2-trifluoromethyl-benzenesulfonamide (0.596 g) as a colorless solid. MS: 417.1 ([M+NH4]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039493B2
Source datasetuspto-grants-2011_10
ORD IDord-dc894f865cda4f85bea1c75c570400e6
Source noteuspto-grants-2011_10