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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1377024Erstellt: 26. Oktober 2026

Hydrochloric Acid → N-{1-[2-(6-Methyl-2-pyridyl)ethyl]-4-piperidyl}-4-(N-methylamino)benzenesulfonamide

https://huagongshe.com/reaction/1377024

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium HydroxideHCID 14798—
Edukt2-Ethenyl-6-methylpyridineHCID 70735—
EduktSodium BicarbonateHCID 516892—
EduktSodium AcetateHCID 517045—
EduktN-(4-piperidyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide acetateHCID 67690431—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
ProduktN-{1-[2-(6-Methyl-2-pyridyl)ethyl]-4-piperidyl}-4-(N-methylamino)benzenesulfonamideHCID 2291893670%

Reaktionsschritte

The N-(4-piperidyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide acetate (3.71 g, 10.0 mmol), 6-methyl-2-vinylpyridine (1.43 g, 12.0 mmol) and sodium acetate (0.82 g) were dissolved in a mixture comprising methanol (20 ml) and water (20 ml). The obtained solution was heated under reflux for 5 hours, followed by the addition of sodium hydroxide (3.20 g). The obtained mixture was heated under reflux for additional three hours and acidified with 2N aqueous hydrochloric acid. The pH of the mixture was adjusted to about 8 with an aqueous solution of sodium hydrogencarbonate. The resulting mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of common salt, dried over magnesium sulfate and concentrated. The obtained oily residue was purified by column chromatography (chloroform:methanol:aqueous ammonia=90:9:1) and recrystallized from ethyl acetate/ether to give the title compound as a white crystal (2.71 g, overall yield of two steps: 70%). m.p. (°C.): 80 to 84

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05663414
Quelldatensatzuspto-grants-1997_09
ORD IDord-a31a93ab971f4668b2de0a3fbc47d964
Quellennotizuspto-grants-1997_09