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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042312Generated: November 1, 2026

Ethyl 3-pyridylacetate → HCID 58133377, compound

https://huagongshe.com/reaction/1042312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-pyridylacetateHCID 96490—
ReactantMethyl 2-aminopyridine-3-carboxylateHCID 351633—
ReactantSodium ethoxideHCID 2723922—
SolventDimethylformamideHCID 6228—
ProductHCID 58133377HCID 58133377—

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of 2-amino-nicotinic acid methyl ester (200 mg) (Example 1.1) in N,N-dimethylformamide (“DMF”) (2 ml) was added sodium ethoxide (21 μl) (21% by weight in ethanol) followed by ethyl-3-pyridyl-acetate (200 μl). The reaction mixture was heated in the microwave at 150° C. for 15 minutes. The mixture was quenched by addition of aqueous hydrochloric acid (2M) (0.72 ml) and then diluted with water. The precipitate was isolated by filtration and washed with water and finally triturated with diethyl ether to give 4-hydroxy-3-pyridin-3-yl-1H-[1,8]naphthyridin-2-one as a beige solid (109 mg). 1H-NMR (400 MHz, d6-DMSO): 11.75 (bs, 1H), 8.70 (m, 1H), 8.52-8.53 (dd, 1H), 8.48-8.49 (dd, 1H), 8.35-8.37 (dd, 1H), 7.98 (d, 1H), 7.45-7.49 (dd, 1H), 7.23-7.26 (dd, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557840B2
Source datasetuspto-grants-2013_10
ORD IDord-ddfd74bd6a684764b93ff9461619c3ee
Source noteuspto-grants-2013_10