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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622928Generated: October 30, 2026

Picolinic acid → HCID 14390489, compound

https://huagongshe.com/reaction/622928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolinic acidHCID 1018—
ReactantThionyl ChlorideHCID 24386—
ReactantEthyl 2-[(3-nitropyridin-2-YL)amino]acetateHCID 14062544—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14390489HCID 14390489—

Reaction Steps

Under a nitrogen atmosphere, triethylamine (0.30 mole) and a solution of freshly prepared acid chloride of 2-pyridine carboxylic acid (0.150 mole), obtained by heating at reflux 2-pyridine carboxic acid and excess thionyl chloride in benzene and then azeotropic distillation with benzene, in dry tetrahydrofuran (50 ml) were added simultaneously (dropwise) to a stirred and chilled (10°-20° C.) solution of freshly prepared N-(3-amino-2-pyridinyl)glycine ethyl ester prepared by reducing N-(3-nitro-2-pyridinyl)glycine ethyl ester (0.106 mole) in 200 ml of dry tetrahydrofuran. The reaction mixture was stirred overnight at room temperature and was filtered. The filtrate was concentrated in vacuo and dissolved in ethyl acetate (250 ml). The solution was washed with saturated sodium bicarbonate solution (3×75 ml), water (2×75 ml), dried over anhydrous sodium sulfate, and concentraed in vacuo. The residue was crystallized from isopropyl ether-tetrahydrofuran giving 26.5 g (83%). A 3.0-g sample was twice recrystallized from isopropyl ether-tetrahydrofuran to give 2.4 g of a white needles, mp 98°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04772600
Source datasetuspto-grants-1988_09
ORD IDord-5f7d68ea3fa04817bfa69219d81464c4
Source noteuspto-grants-1988_09