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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662020Generated: October 25, 2026

Pyridine → Ethyl 4,6-dimethyl-2-oxo-1-phenyl-1,2-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/1662020

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenylboronic AcidHCID 66827—
ReactantEthyl 4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 247443—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 4,6-dimethyl-2-oxo-1-phenyl-1,2-dihydropyridine-3-carboxylateHCID 1383792531.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of ethyl 4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylate (7.5 g, 0.038 mol), phenylboronic acid (14.1 g, 0.115 mol), cupric acetate (1.38 g, 0.008 mol), pyridine (7.5 mL) in 1,4-dioxane (80 mL) is heated at 80° C. for 96 hours. The solid is filtered off and the filtrate is concentrated. The residue is partitioned with EtOAc (50 mL) and 2N HCl (70 mL), and the precipitate is collected by filtration and washed with EtOAc to give the title product (2.95 g). The EtOAc solution is separated, dried and concentrated. The residue is purified by silica gel column chromatography eluting with PE:acetone (2:1) to give another portion of (0.3 g). (3.25 g, 31.2% yield). MS (m/z): 272.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030302B2
Source datasetuspto-grants-2011_10
ORD IDord-57e49fb0763f41c6a6b13c00bfa96d11
Source noteuspto-grants-2011_10