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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238635Generated: October 31, 2026

2-Aminonicotinic acid → Methyl 2-aminopyridine-3-carboxylate

https://huagongshe.com/reaction/2238635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Aminonicotinic acidHCID 72930—
ReactantHydrochloride methanolHCID 21893726—
ProductMethyl 2-aminopyridine-3-carboxylateHCID 351633—

Reaction Conditions

Temperature90 °C

Reaction Steps

The mixture of 138 mg of 2-aminonicotinic acid and 6 mL of hydrochloric acid-methanol solution was stirred overnight in a sealed-tube at 90° C. The reaction mixture was concentrated under reduced pressure, the residue was added with a saturated aqueous solution of sodium hydrogen carbonate, and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, the insolubles were filtered, and the filtrate was concentrated under reduced pressure, to obtain 106 mg of 2-aminonicotinic acid methylester [25-1]. The obtained compound [25-1] was used in the subsequent reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718801B2
Source datasetuspto-grants-2010_05
ORD IDord-0daa06293d5f44b9b7ca85a76e2a2e9e
Source noteuspto-grants-2010_05