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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2216893Erstellt: 25. Oktober 2026

1,10-Phenanthroline → 3-(4-Pyridin-2-yl-imidazol-1-yl)-benzonitrile

https://huagongshe.com/reaction/2216893

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,10-PhenanthrolineHCID 1318—
EduktCesium carbonateHCID 10796—
Edukt3-IodobenzonitrileHCID 144341—
Edukttrans-DibenzylideneacetoneHCID 5354370—
EduktHCID 178420123HCID 178420123—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelO-XyleneHCID 7237—
Produkt3-(4-Pyridin-2-yl-imidazol-1-yl)-benzonitrileHCID 112420368,3%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

To a flame dried, argon purged screw-cap vial, containing copper (I) triflate benzene complex (0.01 g, 0.03 mmol), 1,10-phenanthroline (0.10 g, 0.54 mmol), trans-dibenzylideneacetone (0.01 g, 0.03 mmol) and cesium carbonate (0.20 g, 0.60 mmol) was added a solution of 4-(2-pyridyl)imidazole (0.08 g, 0.54 mmol) and 3-iodobenzonitrile (0.19 g, 0.82 mmol) in ortho-xylene (2 mL). The resulting brownish black reaction mixture was heated overnight at 120° C. After cooling, the reaction mixture was diluted with dichloromethane (20 mL) and washed sequentially with saturated ammonium chloride (20 mL) and brine (20 mL). The organic phase was then dried with sodium sulfate, filtered, and concentrated in vacuo. Silica gel chromatography of the crude residue using 1% methanol (2 M in ammonia) in dichloromethane afforded 11 mg of 4-(2-pyridyl)-1-(3-cyanophenyl)-1H-imidazole, as an off-white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07112595B2
Quelldatensatzuspto-grants-2006_09
ORD IDord-899a4a96a3cf41e4a4fa6d93a65fb868
Quellennotizuspto-grants-2006_09