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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616229Generated: October 27, 2026

Cesium carbonate → 5-(4-acetyl-2-methylphenyl)-1-(2,2-dimethylpropyl)-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one

https://huagongshe.com/reaction/1616229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-Acetyl-2-methylphenyl trifluoromethanesulfonateHCID 21302427—
Reactant[1-(2,2-dimethylpropyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-5-yl]boronic acidHCID 86691828—
CatalystCuprous chlorideHCID 62652—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Product5-(4-acetyl-2-methylphenyl)-1-(2,2-dimethylpropyl)-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-oneHCID 86691843—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a microwave vial, 4-acetyl-2-methylphenyl trifluoromethanesulfonate (34-1) (40 mg, 0.14 mmol), [1-(2,2-dimethylpropyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-5-yl]boronic acid (14-1) (56 mg, 0.22 mmol), cesium carbonate (92 mg, 0.28 mmol), CuCl (14 mg, 0.14 mmol), and Bis(diphenylphosphino)ferrocene dicholoropalladium (8 mg, 0.015 mmol) was added under nitrogen and dissolved in DMF (0.7 ml). The suspension was heated overnight at 100° C. The reaction was cooled to room temperature, 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 5-(4-acetyl-2-methylphenyl)-1-(2,2-dimethylpropyl)-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one (34-2). MS (M+H)+: observed=352.3, calculated=352.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765784B2
Source datasetuspto-grants-2014_07
ORD IDord-bf2b679205c44509b6513e4d1e20764b
Source noteuspto-grants-2014_07