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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497315Generated: October 29, 2026

Diisopropylethylamine → 4-(3-(3-cyanophenyl)ureido)-N-(2,3,6-trifluorobenzyl)benzenesulfonamide

https://huagongshe.com/reaction/497315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2,3,6-TrifluorobenzylamineHCID 2777043—
ReactantHCID 22318884HCID 22318884—
SolventTetrahydrofuranHCID 8028—
Product4-(3-(3-cyanophenyl)ureido)-N-(2,3,6-trifluorobenzyl)benzenesulfonamideHCID 2231890994%

Reaction Steps

4-[3-(3-Cyanophenyl)-ureido]-benzenesulfonyl chloride (1.0 g, 2.98 mmol) was dissolved in 20 ml THF, 2,3,6-trifluoro-benzylamine (0.48 g, 2.98 mmol) and DIEA (0.52 ml, 2.98 mmol) were added and the solution was refluxed for about 3 h. The solvent was removed in vacuo and the residue cristallized with ethanol/water. The solid was filtered and dried in vacuo. Yield 94% of 4-[3-(3-cyano-phenyl)-ureido]-N-(2,3,6-trifluorobenzyl)-benzenesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949567B2
Source datasetuspto-grants-2005_09
ORD IDord-47c449033ea24b609a205cc8747c97d0
Source noteuspto-grants-2005_09