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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1477677Erstellt: 25. Oktober 2026

Tetrahydrofuran → 2-Chloro-4-[4-(4-fluorophenyl)-5,6-dihydropyridin-1(2H)-yl]-1,3,5-triazine

https://huagongshe.com/reaction/1477677

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktSodium CarbonateHCID 10340—
Edukt2,4-Dichloro-1,3,5-triazineHCID 17810—
Edukt4-(4-Fluorophenyl)-1,2,3,6-tetrahydropyridine hydrochlorideHCID 197747—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-Chloro-4-[4-(4-fluorophenyl)-5,6-dihydropyridin-1(2H)-yl]-1,3,5-triazineHCID 11783925185%

Reaktionsschritte

To a tetrahydrofuran (10 mL)-water (4.0 mL) solution of 4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridine hydrochloride (1.43 g, 6.67 mmol) and sodium carbonate (1.56 g, 14.7 mol), 2,4-dichloro-1,3,5-triazine (1.00 g, 6.67 mmol) was added at 0° C. and the resultant mixture was stirred for 1 hour. After completion of the reaction, ethyl acetate was added to the reaction solution and the resultant mixture was washed with each of saturated ammonium chloride aqueous solution and saturated sodium chloride aqueous solution. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform) to obtain the title compound (1.64 g, yield 85%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09403798B2
Quelldatensatzuspto-grants-2016_08
ORD IDord-d3a2d400781c4d889a38cf463dbb9f3d
Quellennotizuspto-grants-2016_08