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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985462Generated: October 29, 2026

Pyridine → N-(3-amino-2-methoxy-5-trifluoromethyl-phenyl)-methanesulfonamide

https://huagongshe.com/reaction/985462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl AcetateHCID 8857—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-Methoxy-5-(trifluoromethyl)benzene-1,3-diamineHCID 22506994—
SolventDichloromethaneHCID 6344—
ProductN-(3-amino-2-methoxy-5-trifluoromethyl-phenyl)-methanesulfonamideHCID 2250698058.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Methoxy-5-trifluoromethylbenzene-1,3-diamine (2.32 g, 11.3 mmol) was dissolved in 50 mL anhydrous dichloromethane. The solution was cooled to 0° C., and pyridine (3.64 mL, 45.0 mmol) and methane sulfonyl chloride (0.89 mL, 11.5 mmol) were added. The reaction was left to stir overnight at room temperature. A few more drops (˜0.1 mL) of methane sulfonyl chloride were added and the reaction stirred an extra day. Then 200 mL EtOAc, was added and the solution washed once with 100 mL water, twice with 15 mL saturated aqueous NH4Cl solution and finally with brine. The organic solution was dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel using EtOAc/hexanes eluent mixtures, providing N-(3-amino-2-methoxy-5-trifluoromethyl-phenyl)-methanesulfonamide (1870 mg, 6.58 mmol, 58% yield) as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06872726B2
Source datasetuspto-grants-2005_03
ORD IDord-c9af3732abda490ea07deb8d079eaa83
Source noteuspto-grants-2005_03