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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520293Generated: November 1, 2026

Toluene → 5-(4-chlorophenyl)-N-methoxy-N-methylpyridine-2-carboxamide

https://huagongshe.com/reaction/1520293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant4-Chlorophenylboronic acidHCID 74299—
Reactant5-Bromo-N-methoxy-N-methylpicolinamideHCID 62952701—
SolventWaterHCID 962—
Product5-(4-chlorophenyl)-N-methoxy-N-methylpyridine-2-carboxamideHCID 11784029739.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

Under a nitrogen atmosphere, a mixture of 5-bromo-N-methoxy-N-methylpyridine-2-carboxamide (2.76 g), 4-chlorophenylboronic acid (2.113 g), 1,1′-bis(diphenylphosphino)ferrocene-palladium(II)dichloride dichloromethane complex (0.920 g), sodium carbonate (3.58 g), toluene (43.3 mL) and water (13 mL) was stirred at 100° C. overnight. To the reaction mixture was added water at room temperature, the mixture was extracted with ethyl acetate, and the extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was fractionated by HPLC(C18, mobile phase: water/acetonitrile (10 mM ammonium hydrogencarbonate-containing system)), the solvent was evaporated under reduced pressure, and the residue was extracted with ethyl acetate. The extract was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give the title compound (1.242 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073864B2
Source datasetuspto-grants-2015_07
ORD IDord-ace7d9666b7c43838eed7b3fe9ee4cff
Source noteuspto-grants-2015_07