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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229645Generated: October 29, 2026

Triethylamine → 3-(2-pyridyl)-5-phenyl-2(1H)-pyridone

https://huagongshe.com/reaction/229645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenylboronic AcidHCID 66827—
Reactant3-(2-Pyridyl)-5-bromo-2-methoxypyridineHCID 22318954—
SolventO-XyleneHCID 7237—
SolventEthyl AcetateHCID 8857—
Product3-(2-pyridyl)-5-phenyl-2(1H)-pyridoneHCID 2231925353.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 1.0 g of 3-(2-pyridyl)-5-bromo-2-methoxypyridine, 0.9 g of phenylboronic acid, 0.3 g of dichlorobistriphenylphosphine palladium and 2 ml of triethylamine was stirred at 120° C. for 1.5 hours in 30 ml of xylene in nitrogen atomosphere. The mixture was returned to room temperature, diluted with ethyl acetate, washed with water and brine, and dried over magnesium sulfate. The solvent was evaporated, and the residue was incorporated with 47% hydrobromic acid and heated at 70° C. for 1 hour. The reaction solution was ice-cooled, diluted with water, and neutralized with potassium carbonate. The resulting precipitates were collected by filtration, washed with water and ether, and then air-dried, to give 0.5 g of the title compound as a pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563811B2
Source datasetuspto-grants-2009_07
ORD IDord-f6c1762f7b4f42e6a3f95e62ee3d46b8
Source noteuspto-grants-2009_07