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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537035Generated: October 30, 2026

Cesium carbonate → 5-[2-(Acetylamino)pyridin-4-yl]-2-(2-chlorophenyl)-3-furoic acid

https://huagongshe.com/reaction/537035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2-Chlorophenylboronic acidHCID 2734322—
ReactantEthyl 5-[2-(acetylamino)pyridin-4-yl]-2-bromo-3-furoateHCID 66748312—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Solvent1,4-DioxaneHCID 31275—
Product5-[2-(Acetylamino)pyridin-4-yl]-2-(2-chlorophenyl)-3-furoic acidHCID 6674831550%

Reaction Steps

To a solution of ethyl 5-[2-(acetylamino)pyridin-4-yl]-2-bromo-3-furoate (0.030 g, 0.09 mmol) in 1,4-dioxane (0.5 mL) and water (0.1 mL) were added tetrakis(triphenylphosphine)palladium(0) (0.010 g, 0.0088 mmol), (2-chlorophenyl)boronic acid (0.018 g, 0.11 mmol), and cesium carbonate (0.087 g, 0.27 mmol). The reaction mixture was subjected to microwave irradiation at 130° C. for 20 min. The reaction mixture was then diluted with water (2 mL) and 1N aqueous sodium hydroxide (0.25 mL) was added. The mixture was allowed to stir at rt overnight. The reaction mixture was extracted with EtOAc and the organic solutions were combined and concentrated. The residue was purified by column chromatography to give 5-[2-(acetylamino)pyridin-4-yl]-2-(2-chlorophenyl)-3-furoic acid (0.015 g, 50%) as a white solid. LCMS (FA): m/z=357.4 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859768B2
Source datasetuspto-grants-2014_10
ORD IDord-8fa2868fe98d49e692969641acc58991
Source noteuspto-grants-2014_10