Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 248022Erstellt: 25. Oktober 2026

Triethylamine → N-(pyridin-2-ylmethyl)methanesulfonamide

https://huagongshe.com/reaction/248022

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-PyridinemethanamineHCID 19509—
EduktMethanesulfonyl chlorideHCID 31297—
EduktSodium BicarbonateHCID 516892—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(pyridin-2-ylmethyl)methanesulfonamideHCID 465700176,8%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a 0° solution of 15 g of 2-(aminomethyl)pyridine, 15.44 g of triethylamine and 150 ml of methylene chloride is added 17.48 g of methanesulfonyl chloride in 100 ml of methylene chloride. The mixture is stirred at 0° C. for 1 hour followed by stirring at room temperature for 3 hours. The reaction is poured into saturated sodium bicarbonate and extracted with methylene chloride. The combined extracts are washed with saturated sodium chloride and concentrated in vacuo. The residue is purified by chromatography (silica gel: 10% methyl alcohol/ethyl acetate) to give 19.84 g of the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05208247
Quelldatensatzuspto-grants-1993_05
ORD IDord-9e181e15af8d430ab55c46ae28c7b1fb
Quellennotizuspto-grants-1993_05