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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 524905Erstellt: 24. Oktober 2026

Thioacetic acid → HCID 90199365, Verbindung

https://huagongshe.com/de/reaction/524905

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThioacetic acidHCID 10484—
EduktTriphenylphosphineHCID 11776—
EduktDiisopropyl azodicarboxylateHCID 5363146—
EduktHCID 86720960HCID 86720960—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 90199365HCID 90199365—

Reaktionsschritte

isopropyl (NE)-N-isopropoxycarbonyliminocarbamate (723.1 mg, 3.576 mmol) was added dropwise to a solution of 1-(3-chloro-5-fluoro-4-pyridyl)piperidin-4-ol (750 mg, 3.251 mmol) and Triphenylphosphine (937.9 mg, 828.5 μL, 3.576 mmol) in THF at −20° C. After stirring for 15 mins, ethanethioic S-acid (272.2 mg, 255.6 μL, 3.576 mmol) was added, the mixture was allowed to warm to room temperature and was stirred for a further 30 minutes. The mixture was then diluted with ethylacetate (30 ml), washed twice with water (20 ml) and with brine. The organic layer was dried with MgSO4 and concentrated in vacuo to a yellow solid that was purified by column chromatography eluting with 5/95 ether/pet ether to elute side products and then 10/90 ether/pet ether. The relevant fractions were combined and concentrated in vacuo to afford S-(1-(3-chloro-5-fluoropyridin-4-yl)piperidin-4-yl) ethanethioate as a green solid. MS (ES+) 289.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09340546B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-084a3e97478741ebbc630aeacb88ad29
Quellennotizuspto-grants-2016_05