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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406Generated: October 25, 2026

Pyridine → N-(2-Methoxyphenyl)-3-pyridinesulfonamide

https://huagongshe.com/reaction/2406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-MethoxyanilineHCID 7000—
ReactantSodium CarbonateHCID 10340—
ReactantPyridine-3-sulfonyl chloride hydrochlorideHCID 12571517—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductN-(2-Methoxyphenyl)-3-pyridinesulfonamideHCID 1968995883.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

o-Anisidine (377 mg, 3.0 mmol) was dissolved in toluene (10 ml) to which were subsequently added pyridine (0.48 ml, 6.0 mmol) and 3-pyridinesulfonylchloride hydrochloride (642 mg, 3.0 mmol) at room temperature. After 1.5 hours of stirring at 100° C., the resulting reaction solution was mixed with water (20 ml), adjusted to pH 7 to 8 with anhydrous sodium carbonate, extracted with ethyl acetate and then washed with water and saturated brine. After drying on anhydrous sodium carbonate and removing the solvent by evaporation, the resulting orange solid was purified by a silica gel column chromatography (ether:hexane=3:1) to obtain a light orange solid which was subsequently washed with an ether-hexane (1:3) mixture solution to obtain 662 mg (83.5%) of the title compound in the form of colorless prism crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728835
Source datasetuspto-grants-1998_03
ORD IDord-3ced4cee9a3c4c979b4e3a0eb0a11cbb
Source noteuspto-grants-1998_03