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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 378290Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/378290

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4,6-Dichloro-n-methylpyrimidin-2-amineHCID 259880—
Edukt4-Fluoro-benzenesulfonamide potassium saltHCID 131721324—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktN-(6-chloro-2-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamideHCID 1935354456%

Reaktionsschritte

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. 121-123C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06030976
Quelldatensatzuspto-grants-2000_02
ORD IDord-ba76fd18be1544219176b04f09dfd7fd
Quellennotizuspto-grants-2000_02