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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1883011Erstellt: 25. Oktober 2026

Tetrahydrothiopyran-4-one → 5-Chloro-N-(5-methylpyridin-2-yl)-2-{[1-(tetrahydrothiopyran-4-yl)piperidin-4-yl]methyl-amino}benzamide

https://huagongshe.com/reaction/1883011

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrothiopyran-4-oneHCID 66173—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt5-Chloro-N-(5-methylpyridin-2-yl)-2-[(4-piperidinylmethyl)amino]benzamideHCID 21906309—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelAcetic acid methanolHCID 10129899—
Produkt5-Chloro-N-(5-methylpyridin-2-yl)-2-{[1-(tetrahydrothiopyran-4-yl)piperidin-4-yl]methyl-amino}benzamideHCID 2190656140,1%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

5-Chloro-N-(5-methylpyridin-2-yl)-2-[(4-piperidinylmethyl)amino]benzamide from Example 99-A (0.45 g, 1.25 mmol) was dissolved in 95:5 methanol-acetic acid (10 mL), followed by addition of tetrahydrothiopyran-4-one (1.46 g, 12.6 mmol) and sodium cyanoborohydride (5.0 mL of a 1 M solution in tetrahydrofuran, 6.0 mmol). After stirring at 50° C. for 96 h, the mixture was concentrated in vacuo; and the residue was directly subjected to silica gel chromatography. Elution with 9:1 dichloromethane-methanol provided 0.23 g (40%) of the title product as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06759414B2
Quelldatensatzuspto-grants-2004_07
ORD IDord-c70133b81bce499faecbf868b89a6754
Quellennotizuspto-grants-2004_07