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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657487Generated: October 28, 2026

3-(Difluoromethoxy)aniline → N-[3-(Difluoromethoxy)phenyl]-4-methyl-3-[4-(2,2,2-trifluoroacetyl)-1-piperazinyl]benzenesulfonamide

https://huagongshe.com/reaction/657487

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Difluoromethoxy)anilineHCID 2774110—
ReactantHCID 59563966HCID 59563966—
SolventPyridineHCID 1049—
ProductN-[3-(Difluoromethoxy)phenyl]-4-methyl-3-[4-(2,2,2-trifluoroacetyl)-1-piperazinyl]benzenesulfonamideHCID 5956397247.3%

Reaction Steps

0.429 g of 3-(difluoromethoxy)-aniline (2.7 mmol) were dissolved in 5 mL of pyridine. 1 g of 4-methyl-3-[4-(2,2,2-trifluoro-acetyl)-piperazin-1-yl]-benzenesulfonylchloride (2.7 mmol) were added slowly at room temperature. After stirring for 16 h at room temperature, the reaction mixture was evaporated several times after addition of toluene. The residue was dissolved in dichloromethane and washed several times with 5% aqueous ammonium chloride. The organic phase was then washed with saturated aqueous sodium chloride, dried over sodium sulphate, filtered, and the solvent evaporated. The crude product was purified via silica gel chromatography using dichloromethane/methanol (0-5%) to yield 0.63 g of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076326B2
Source datasetuspto-grants-2011_12
ORD IDord-6a2ff749fa604e1abaa2b5f9f2045ebc
Source noteuspto-grants-2011_12