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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 378291Erstellt: 25. Oktober 2026

Triethylamine → N-(2,6-bis-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamide

https://huagongshe.com/reaction/378291

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethylamine hydrochlorideHCID 6364545—
EduktN-(6-chloro-2-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamideHCID 19353544—
LösungsmittelEthanolHCID 702—
ProduktN-(2,6-bis-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamideHCID 1777452243,8%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

0.36 g (0.0011 mol) of N-(6-chloro-2-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamide was dissolved in 10 ml of ethanol, treated with 1.2 g (0.018 mol) of methylamine hydrochloride and 4.0 ml (0.029 mol) of triethylamine and stirred in an autoclave at 140° C. for 17 hours. The mixture was freed completely from solvent, the residue was partitioned in ethyl acetate/water, the insoluble constituents were filtered off under suction and extracted. The extract and the solid were combined and recrystallized from methanol/diethyl ether. There was obtained 0.15 g (43%) of N-(2,6-bis-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamide as white crystals; m.p. 261-263° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06030976
Quelldatensatzuspto-grants-2000_02
ORD IDord-e43e829c2ce54c36ab02dad425a4882b
Quellennotizuspto-grants-2000_02