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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120071Generated: October 31, 2026

Hydrochloric Acid → Ethyl 5-aminopyridine-2-carboxylate

https://huagongshe.com/reaction/2120071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
Reactant5-Aminopyridine-2-carboxylic acidHCID 4179726—
ProductEthyl 5-aminopyridine-2-carboxylateHCID 13816714—

Reaction Conditions

Temperature23 °C

Reaction Steps

A stirred suspension of 3-amino-pyridine-6-carboxylic acid (25 g) in ethanol (300 mL) at 0° C. was saturated with gaseous hydrogen chloride. The mixture was allowed to warm to 23° C. and heated to reflux for 2 hours. A clear solution was obtained. After cooling to 23° C., the mixture was concentrated in vacuo, neutralized with aqueous NaHCO3 and extracted with ethyl acetate. The organic phase was washed with water, dried over MgSO4, and concentrated in vacuo to give ethyl 3-amino-pyridine-6-carboxylate as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689754B1
Source datasetuspto-grants-2004_02
ORD IDord-2d07cdb8725146c799a144402ccdec56
Source noteuspto-grants-2004_02