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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246436Generated: November 1, 2026

Potassium Carbonate → 2-dimethylamino-6-(4-ethoxy-3-trifluoromethyl-phenyl)-1H-imidazo[4,5-c]pyridine-4-carbonitrile

https://huagongshe.com/reaction/2246436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Ethoxy-3-(trifluoromethyl)benzeneboronic acidHCID 44558184—
Reactant6-chloro-2-dimethylamino-1H-imidazo[4,5-c]pyridine-4-carbonitrileHCID 58938132—
SolventTetrahydrofuranHCID 8028—
Product2-dimethylamino-6-(4-ethoxy-3-trifluoromethyl-phenyl)-1H-imidazo[4,5-c]pyridine-4-carbonitrileHCID 589381233%

Reaction Conditions

Temperature130 °C

Reaction Steps

A suspension of 6-chloro-2-dimethylamino-1H-imidazo[4,5-c]pyridine-4-carbonitrile (100 mg, 0.45 mmol), 4-ethoxy-3-trifluoromethyl-phenyl boronic acid (198 mg, 0.88 mmol) tetrakis(triphenylphosphine)palladium(0) (50 mg, ˜10 mol %) and potassium carbonate (193.0 mg, 1.39 mmol) in THF (3 ml) was heated to 130° C. for 6 minutes in the “Smith” microwave. The crude mixture was concentrated under reduced pressure to remove THF before partitioning between ethyl acetate and water. The organic layer was separated, dried over sodium sulfate and concentrated under reduced pressure. The material was then dissolved in DMSO and purified in aliquots by preparative HPLC. The desired fractions were collected and concentrated to give a white solid which was washed with ether to afford 2-dimethylamino-6-(4-ethoxy-3-trifluoromethyl-phenyl)-1H-imidazo[4,5-c]pyridine-4-carbonitrile (5.0 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687515B2
Source datasetuspto-grants-2010_03
ORD IDord-102f7f63ac584b16ad4ba8611f9f5416
Source noteuspto-grants-2010_03