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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616213Generated: October 29, 2026

Sodium Bicarbonate → 2-(3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-5-yl)benzonitrile

https://huagongshe.com/reaction/1616213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant2-(2-Cyanophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 3570229—
Reactant5-chloro-3-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-oneHCID 55269061—
CatalystHCID 178418851HCID 178418851—
SolventMethanolHCID 887—
Product2-(3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-5-yl)benzonitrileHCID 86691821—

Reaction Conditions

Temperature100 °C

Reaction Steps

5-chloro-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one (1-3) (74 mg, 0.4 mmol), 2-cyanophenylboronic acid pinacol ester (179 mg, 1.2 mmol), sodium bicarbonate (200 mg, 2.4 mmol), and bis(tri-t-butylphosphine)palladium(0) (61 mg, 0.12 mmol) were added to a microwave vial and purged with nitrogen. Dioxane (1.2 mL) was added, the vessel was sealed and the suspension was heated at 100° C. for 12 minutes in a microwave reactor. The cooled reaction was diluted with methanol, and passed through a syringe filter. The solution was purified using reverse phase chromatography (10-100%, 0.1% TFA in H2O/Acetonitrile) and the desired fractions were collected and concentrated to produce 2-(3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-5-yl)benzonitrile (4-1). MS (M+H)+: observed=251.1, calculated=251.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765784B2
Source datasetuspto-grants-2014_07
ORD IDord-8809cbeebcca4ac298a86b731081f01d
Source noteuspto-grants-2014_07