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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82230Generated: October 27, 2026

Picolinic acid → Ethyl 1,5-naphthyridin-3-ylacetate

https://huagongshe.com/reaction/82230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolinic acidHCID 1018—
ReactantCesium carbonateHCID 10796—
Reactant2,2-DiethylpropanedioateHCID 6951563—
Reactant3-Bromo-1,5-naphthyridineHCID 12878818—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 1,5-naphthyridin-3-ylacetateHCID 70817520402.5%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 3-bromo-1,5-naphthyridine (540 mg, 2.58 mmol), diethylmalonate (0.8 mL, 5.17 mmol) and cesium carbonate (2.53 g, 7.75 mmol) in 1,4-dioxane (6 mL) was degassed with argon for 15 min then picolinic acid (64 mg, 0.517 mmol) and CuI (50 mg, 0.258 mmol) was added. The mixture was heated in a sealed tube at 110° C. for 24 hours then cooled to room temperature, diluted with ethyl acetate (10 mL), washed with water (10 mL) and brine (10 mL). The organic phase was dried over sodium sulphate then evaporated in vacuo and purified by column chromatography on silica gel (hexane:EtOAc 70:30) to afford 450 mg of ethyl 1,5-naphthyridin-3-ylacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846698B2
Source datasetuspto-grants-2014_09
ORD IDord-dbf074aa3cb349a3be97092eb8999ff6
Source noteuspto-grants-2014_09