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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399801Generated: November 1, 2026

Hydrochloric Acid → Methyl 5-aminopyridine-3-carboxylate

https://huagongshe.com/reaction/399801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-(tert-butoxycarbonylamino)nicotinateHCID 18945232—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductMethyl 5-aminopyridine-3-carboxylateHCID 151443259%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of methyl 5-tert-butoxycarbonylamino-3-pyridinecarboxylate (5.7 g) and conc. hydrochloric acid (11.4 ml) in methanol (57 ml) was stirred for 1 hour at 40° C. After being cooled to room temperature, the reaction mixture was poured into a mixture of ethyl acetate (100 ml) and water (50 ml) under stirring, and adjusted to pH 9.0 with 10% potassium carbonate aqueous solution. The organic layer was washed with brine and dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was recrystallized from diethyl ether-methanol to afford methyl 5-amino-3-pyridinecarboxylate (2.03 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05824691
Source datasetuspto-grants-1998_10
ORD IDord-9bd0f208d6964ccab1cec09a84c2b1dd
Source noteuspto-grants-1998_10