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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838258Generated: November 2, 2026

4-Fluoroaniline → trans-4-(4-Cyano-3-trifluoromethylphenyl)-N-(4-fluorophenyl)-2,5-dimethylpiperazine-1-sulfonamide

https://huagongshe.com/reaction/1838258

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluoroanilineHCID 9731—
ReactantSulfamideHCID 82267—
Reactanttrans-4-(2,5-Dimethylpiperazin-1-yl)-2-trifluoromethylbenzonitrileHCID 11391932—
SolventPyridineHCID 1049—
Producttrans-4-(4-Cyano-3-trifluoromethylphenyl)-N-(4-fluorophenyl)-2,5-dimethylpiperazine-1-sulfonamideHCID 69108864—

Reaction Steps

A 1.21 g portion of trans-4-(2,5-dimethylpiperazin-1-yl)-2-trifluoromethylbenzonitrile synthesized in Reference Example 1-1 and 2.05 g of sulfamide were heated under reflux for 1.5 hours in 15 ml of pyridine. Next, this was mixed with 4.05 ml of 4-fluoroaniline and again heated under reflux for 4 hours. After evaporation of the solvent, the residue was purified by a silica gel column chromatography to obtain 701 mg of the title compound from toluene-ethyl acetate eluate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673799B1
Source datasetuspto-grants-2004_01
ORD IDord-50d8bb59c75a49fe9182e1b8d5d09c23
Source noteuspto-grants-2004_01