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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479746Generated: October 29, 2026

Benzonitrile → Pyridine, 4-[2-(4-methoxyphenyl)-1-methyl-4-phenyl-1H-imidazol-5-yl]-

https://huagongshe.com/reaction/479746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrileHCID 7505—
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Methoxy-N-methyl-N-(4-picolyl)benzamideHCID 15407880—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductPyridine, 4-[2-(4-methoxyphenyl)-1-methyl-4-phenyl-1H-imidazol-5-yl]-HCID 1026889017%

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a solution of diisopropylamine (0. 16 mL, 1.1 mmol) in THF at −78° C. was added n-butyllithium (0.38 mL of 2.5 M solution, 0.95 mmol). To the resulting mixture was added a solution of 4-methoxy-N-methyl-N-(4-picolyl)benzamide (0.16 g, 0.62 mmol) in THF. The resulting dark red solution was warmed to −40° C. and stirred for 15 min, at which time benzonitrile (0.13 mL, 1.2 mmol) was added. The mixture to warmed to rt and stirred for 10 h. Aqueous NH4Cl (0.5 mL) was added, and the mixture was concentrated under reduced pressure. The residue was purified by flash chromatography, eluting with a solvent gradient of 2-4% MeOH/CHCl3. The material which was isolated was triturated with Et2O and recrystallized from EtOAc to provide the title compound as an off-white solid (35 mg, 17%): mp 193-194° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06645989B2
Source datasetuspto-grants-2003_11
ORD IDord-2e396d627e7a407e965555ce66e17bbc
Source noteuspto-grants-2003_11