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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610818Generated: October 25, 2026

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

https://huagongshe.com/reaction/610818

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-Dichloro-n-methylpyrimidin-2-amineHCID 259880—
Reactant4-Fluoro-benzenesulfonamide potassium saltHCID 131721324—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-(6-chloro-2-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamideHCID 1935354456%

Reaction Steps

0.46 g (0.0026 mol) of (4,6-dichloro-pyrimidin-2-yl)-methylamine and 1.1 g (0.0051 mol) of 4-fluoro-benzenesulfonamide potassium salt were stirred in 10 ml of 1-methyl-2-pyrrolidone in 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 saturated with sodium chloride, evaporated briefly in a vacuum and made acid with 4N HCl, with a precipitate separating. The mixture was suctioned filtered, the extract and the solid were combined and chromatographed over silica gel with cyclohexane/ethyl acetate 2:1 as the eluent. The product was recrystallized from ethyl acetate/n-hexane. There was obtained 0.46 g (56%) of N-(6-chloro-2-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamide as white crystals; m.p. 121-123 C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998665
Source datasetuspto-grants-1999_12
ORD IDord-a5c988261e8745bcb6cc6891b8d5b359
Source noteuspto-grants-1999_12