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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047588Generated: November 2, 2026

Water → Ethyl 5-bromo-5'-methyl-2,3'-bipyridine-4-carboxylate

https://huagongshe.com/reaction/2047588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant5-Methylpyridine-3-boronic acidHCID 2762708—
ReactantEthyl 2,5-dibromoisonicotinateHCID 46311329—
SolventDimethylformamideHCID 6228—
ProductEthyl 5-bromo-5'-methyl-2,3'-bipyridine-4-carboxylateHCID 58394285—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution ethyl 2,5-dibromoisonicotinate (1-2, 1.5 g, 4.86 mmol) in degassed dimethylformamide (24 mL) at 25° C. was added (5-methylpyridin-3-yl)boronic acid (0.665 g, 4.86 mmol), PdCl2dppf (0.355 g, 0.486 mmol), cesium carbonate (4.75 g, 14.6 mmol) and water (0.262 mL, 14.57 mmol). The reaction flask was purged with nitrogen, sealed and stirred at 50° C. overnight. The crude reaction mixture was partitioned between water and EtOAc, separating layers and washing the organic layer with saturated sodium bicarbonate solution and brine. The solvent was removed by rotary evaporation and the crude product was purified by normal phase column chromatography (0 to 50% EtOAc in hexanes) to afford the product (1-3) as a white solid. ESI+MS[M]+C14H13BrN2O2=321.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592457B2
Source datasetuspto-grants-2013_11
ORD IDord-5ebfb4a674c04f07ae2a65ce5bfc633e
Source noteuspto-grants-2013_11