Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1081750Erstellt: 26. Oktober 2026

Sodium Methoxide → 5-[1-(Methylsulfonyl)-4-piperidylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1081750

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium MethoxideHCID 10942334—
Edukt1-(Methylsulfonyl)piperidin-4-yl methanesulfonateHCID 22273065—
EduktHCID 178418687HCID 178418687—
LösungsmittelEthanolHCID 702—
LösungsmittelMethanolHCID 887—
Produkt5-[1-(Methylsulfonyl)-4-piperidylthio]imidazo[1,2-a]pyridineHCID 2008666040,8%

Reaktionsschritte

To a suspension of 5-mercaptoimidazo[1,2-a]pyridine (1.50 g, 10 moles) in ethanol (100 ml) was added a solution of 4.1M sodium methylate (2.44 ml, 10 mmoles) in methanol and the mixture was stirred at room temperature for 10 minutes. To the reaction mixture was added 1-methylsulfonyl-4-methylsulfonyloxypiperidine (2.83 g, 11 mmoles) at room temperature and the mixture was heated under reflux for 14 hours. After the solvent was distilled off, the residue was dissolved in chloroform, which was washed in turn with an aqueous 1N sodium hydroxide solution and water and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography [eluent:ethyl acetate/ethanol (10:1)] to obtain 1.27 g of the desired product (40.8%, light brown solid).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05587383
Quelldatensatzuspto-grants-1996_12
ORD IDord-6bf4187ea4814b69931712d96d6048e1
Quellennotizuspto-grants-1996_12