Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072920Generated: October 31, 2026

Picolinic acid → HCID 14390489, compound

https://huagongshe.com/reaction/2072920

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 concentrated 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 numberUS04914109
Source datasetuspto-grants-1990_04
ORD IDord-c83e53f230cc46548fb68a1848314351
Source noteuspto-grants-1990_04