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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2232407Erstellt: 26. Oktober 2026

Potassium Carbonate → N-Methyl-4-[4-(4-pyridyl)piperazin-1-yl]benzenesulphonamide

https://huagongshe.com/reaction/2232407

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt1-(4-Pyridyl)piperazineHCID 70517—
Edukt4-fluoro-N-methylbenzene-1-sulfonamideHCID 2440054—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktN-Methyl-4-[4-(4-pyridyl)piperazin-1-yl]benzenesulphonamideHCID 212835366,9%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 1-(4-pyridyl)piperazine (0.86 g), N-methyl-4-fluorobenzenesulphonamide (1.00 g) and potassium carbonate (2.00 g) in N-methylpyrrolidone was stirred at 100° C. for 24 hours and then evaporated. The residue was partitioned between dichloromethane and 2N hydrochloric acid. The acid layer was washed with dichloromethane, filtered and made basic with sodium bicarbonate solution. The mixture was extracted several times with chloroform, and the combined extracts were washed with water, dried over magnesium sulphate and evaporated. The residue was crystallised from ethanol/ethyl acetate to give the title compound (0.12 g), m.p. 204°-206° C. Found: C,57.55; H,6.13; N,16.62. C16H20N4O2S requires: C,57.81; H,6.06; N,16.85%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04788196
Quelldatensatzuspto-grants-1988_11
ORD IDord-542a1ec6e4ad4a5d9140fb585b095058
Quellennotizuspto-grants-1988_11