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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432003Generated: October 24, 2026

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

https://huagongshe.com/en/reaction/432003

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,10-PhenanthrolineHCID 1318—
ReactantCesium carbonateHCID 10796—
Reactant3-IodobenzonitrileHCID 144341—
Reactanttrans-DibenzylideneacetoneHCID 5354370—
ReactantHCID 178420123HCID 178420123—
SolventDichloromethaneHCID 6344—
SolventO-XyleneHCID 7237—
Product3-(4-Pyridin-2-yl-imidazol-1-yl)-benzonitrileHCID 112420368.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

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 (0.20g, 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660753B2
Source datasetuspto-grants-2003_12
ORD IDord-16b5d23edf5a421c90fe9c73a295dcbc
Source noteuspto-grants-2003_12