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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 647511Erstellt: 25. Oktober 2026

Thiophenol → 4-Acetamido-1-(6-phenylthio-2-pyridyl)piperidine

https://huagongshe.com/reaction/647511

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThiophenolHCID 7969—
EduktPotassium CarbonateHCID 11430—
Edukt2,6-DichloropyridineHCID 16989—
EduktN-Pyridin-4-ylacetamideHCID 21288—
EduktSodiumHCID 5360545—
Edukt2-Chloro-6-(phenylthio)pyridineHCID 12760118—
LösungsmittelSulfolaneHCID 31347—
Produkt4-Acetamido-1-(6-phenylthio-2-pyridyl)piperidineHCID 1292661748,5%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

A mixture of 9.5 g of 2-chloro-6-(phenylthio) pyridine (b.p. 112° to 116° C./0.01 mm Hg, prepared by reaction of 2,6-dichloropyridine with the sodium salt of thiophenol), 7.8 g of potassium carbonate and 7.6 g of 4-acetamidopyridine in 75 ml of sulfolane is heated to 150° C. with stirring for 50 hours, then the sulfolane is concentrated to 1/5th of its volume, the mixture is poured in 100 ml of water and extraction is effected four times with 150 ml of diethyl ether. The organic phase is washed with water, dried over anhydrous sodium sulfate, concentrated to dryness and the residue is crystallised in 40 ml of ethyl acetate. 6.8 g of 4-acetamido-1-(6-phenylthio-2-pyridyl)piperidine are thus obtained; m.p. 110° to 112° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04409228
Quelldatensatzuspto-grants-1983_10
ORD IDord-617e70658e0147dbba88ec38debf31af
Quellennotizuspto-grants-1983_10