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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378296Generated: October 26, 2026

4,6-Dichloro-n-methylpyrimidin-2-amine → N-(6-chloro-2-methylamino-pyrimidin-4-yl)-3-trifluoromethyl-benzenesulfonamide

https://huagongshe.com/reaction/378296

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-Dichloro-n-methylpyrimidin-2-amineHCID 259880—
Reactant3-Trifluoromethyl-benzenesulfonamide potassium saltHCID 131721326—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-(6-chloro-2-methylamino-pyrimidin-4-yl)-3-trifluoromethyl-benzenesulfonamideHCID 1935353769%

Reaction Steps

0.27 g (0.00155 mol) of (4,6-dichloro-pyrimidin-2-yl)-methylamine and 0.82 g (0.0031 mol) of 3-trifluoromethyl-benzenesulfonamide potassium salt were stirred in 10 ml of 1-methyl-2-pyrrolidone at 150° C. for 8 hours. Then, the solvent was distilled off in a high vacuum, the residue was partitioned in ethyl acetate/water and extracted. The aqueous phase was made acid with 4N HCl and extracted with dichloromethane. The residue was chromatographed over silica gel with cyclohexane/ethyl acetate 2:1 as the eluent. There was obtained 0.26 g (69%) of N-(6-chloro-2-methylamino-pyrimidin-4-yl)-3-trifluoromethyl-benzenesulfonamide as white/beige crystals; m.p.: 190-193° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030976
Source datasetuspto-grants-2000_02
ORD IDord-833f8bf98a7342de8cfe5455fbcb6382
Source noteuspto-grants-2000_02