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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014717Generated: October 25, 2026

Potassium Carbonate → 3-(1-Phenylethyl)-5-(quinolin-5-YL)-1H-imidazo[4,5-B]pyridin-2(3H)-one

https://huagongshe.com/reaction/1014717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantQuinolin-5-ylboronic acidHCID 5153389—
Reactant6-chloro-3-nitro-N-(1-phenylethyl)pyridin-2-amineHCID 43330321—
Reactant3-Nitro-N-(1-phenylethyl)-6-(quinolin-5-yl)pyridin-2-amineHCID 66699881—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-(1-Phenylethyl)-5-(quinolin-5-YL)-1H-imidazo[4,5-B]pyridin-2(3H)-oneHCID 2498468079%

Reaction Conditions

Temperature85 °C

Reaction Steps

3-Nitro-N-(1-phenylethyl)-6-(quinolin-5-yl)pyridin-2-amine. To a solution of 6-chloro-3-nitro-N-(1-phenylethyl)pyridin-2-amine (2.24 g, 8.07 mmol) and quinolin-5-ylboronic acid (1.81 g, 10.5 mmol) in DMF (150 mL) was added potassium carbonate (4.46 g, 32.3 mmol) in water (25 mL). The reaction solution was purged with a stream of nitrogen followed by the addition of tetrakis(triphenylphosphine)palladium(0) (932 mg, 0.81 mmol). After heating at 85° C. for 2 h, the solvent was removed under reduced pressure. The crude product was purified by silica gel chromatography to afford the title compound (2.36 g, 79% yield). MS (ESI) m/z 371.3 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981893B2
Source datasetuspto-grants-2011_07
ORD IDord-fcf5d008b09942b1a76cd25daa858666
Source noteuspto-grants-2011_07