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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514014Generated: October 31, 2026

Potassium Carbonate → 2-(5-Chloro-2-methoxyphenyl)pyridin-3-amine

https://huagongshe.com/reaction/1514014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-3-pyridylamineHCID 80528—
Reactant5-Chloro-2-methoxyphenylboronic acidHCID 2735751—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-(5-Chloro-2-methoxyphenyl)pyridin-3-amineHCID 68734812—

Reaction Steps

The 500 mL round-bottom flask, equipped with magnetic stirrer and reflux condenser was charged with 5-chloro-2-methoxyphenylboronic acid (9.78 g, 52 mmol), 3-amino-2-chloropyridine (7.00 g, 55 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (S-Phos, 0.43 g, 2 mol %), palladium (II) acetate (112 mg, 1 mol %), potassium carbonate (21.7 g, 157 mmol), 180 mL of acetonitrile and 20 ml of water. The flask was filled with nitrogen and heated to reflux under nitrogen atmosphere for 24 hours. Then the reaction was cooled down to room temperature, diluted with 500 mL of water and extracted with ethyl acetate (5×40 mL). Organic fractions were combined, dried over sodium sulfate, filtered and evaporated. The residue was subjected to column chromatography on silica gel with eluent hexane/ethyl acetate gradient mixture, providing 2-(5-chloro-2-methoxyphenyl)pyridin-3-amine as white crystals (9.5 g, NMR confirmed the structure).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08221905B2
Source datasetuspto-grants-2012_07
ORD IDord-7b2ade70cd0c43f5b65ba332df0f3cb6
Source noteuspto-grants-2012_07