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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1718572Erstellt: 26. Oktober 2026

Dimethylformamide → 4'-{[1-(3-Acetylbenzyl)-4-butyl-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}biphenyl-2-carbonitrile

https://huagongshe.com/reaction/1718572

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPotassium CarbonateHCID 11430—
Edukt1-(3-(Bromomethyl)phenyl)ethan-1-oneHCID 15479807—
Edukt4'-[(4-Butyl-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl)methyl]biphenyl-2-carbonitrileHCID 135401222—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4'-{[1-(3-Acetylbenzyl)-4-butyl-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}biphenyl-2-carbonitrileHCID 57460474—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of 4′-[(4-butyl-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl)methyl]biphenyl-2-carbonitrile (1.22 g), potassium carbonate (0.94 g), 1-[3-(bromomethyl)phenyl]ethanone (0.73 g) and N,N-dimethylformamide (20 mL) was stirred at 90° C. for 2 hr. The reaction mixture was diluted with ethyl acetate, washed with water and then with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography to give the title compound as a colorless viscous substance (1.02 g, 61%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07803940B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-563a47c33888490a9aba357224902793
Quellennotizuspto-grants-2010_09