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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Thiophenol | HCID 7969 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2,6-Dichloropyridine | HCID 16989 | — |
| Edukt | N-Pyridin-4-ylacetamide | HCID 21288 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Edukt | 2-Chloro-6-(phenylthio)pyridine | HCID 12760118 | — |
| Lösungsmittel | Sulfolane | HCID 31347 | — |
| Produkt | 4-Acetamido-1-(6-phenylthio-2-pyridyl)piperidine | HCID 12926617 | 48,5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04409228 |
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| Quelldatensatz | uspto-grants-1983_10 |
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| ORD ID | ord-617e70658e0147dbba88ec38debf31af |
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| Quellennotiz | uspto-grants-1983_10 |
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