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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497808Generated: October 31, 2026

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

https://huagongshe.com/reaction/497808

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 2231925327.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 11.0 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 numberUS06949571B2
Source datasetuspto-grants-2005_09
ORD IDord-37dd760c7ce44807ac40783d2f848ce3
Source noteuspto-grants-2005_09