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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13307Generated: October 26, 2026

Potassium Nitrate → 5-Fluoro-4-(6-ethanesulfonyl-pyridin-3-yloxy)-2-nitro-phenylamine

https://huagongshe.com/reaction/13307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium NitrateHCID 24434—
Reactant3-Fluoro-4-(6-ethanesulfonyl-pyridin-3-yloxy)-phenylamineHCID 23145605—
SolventTrifluoroacetic acidHCID 6422—
Product5-Fluoro-4-(6-ethanesulfonyl-pyridin-3-yloxy)-2-nitro-phenylamineHCID 23145095—

Reaction Steps

3.8 g of potassium nitrate was added to a trifluoroacetic acid (100 ml) solution of 10.5 g of 3-fluoro-4-(6-ethanesulfonyl-pyridin-3-yloxy)-phenylamine, and the reaction liquid was stirred for 1 hour at room temperature, and the solvent was evaporated away under reduced pressure. The residue was diluted with ethyl acetate, washed with aqueous saturated sodium bicarbonate and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=1/2) to obtain the entitled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728025B2
Source datasetuspto-grants-2010_06
ORD IDord-37e3c2824ee24e1991bba8bd626a02a6
Source noteuspto-grants-2010_06