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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215687Generated: November 4, 2026

Methanol → Methyl 2-aminopyridine-3-carboxylate

https://huagongshe.com/reaction/215687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Aminonicotinic acidHCID 72930—
ProductMethyl 2-aminopyridine-3-carboxylateHCID 35163355%

Reaction Steps

42.4 g (356.4 mmol, 26 ml) thionyl chloride was added dropwise to a suspension of 15.0 g (108.6 mmol) 2-aminonicotinic acid in 150 ml abs. Methanol, while cooling. The mixture was heated to reflux and the mixture was refluxed for 19 hours. The evolving SO2 was scrubbed. The solvent was removed under reduced pressure after cooling down to room temperature. The residue was carefully treated with a satured NaHCO3 solution and extracted with ethyl acetate. The organic fraction was dried over magnesium sulfate and the solvent was evaporated under reduced pressure. 9.13 g (55%) of 2-aminonicotinic acid methyl ester was isolated as a pale yellow solid (m.p. 83° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08192918B2
Source datasetuspto-grants-2012_06
ORD IDord-44311b2c45b94b29b982197b92097dfa
Source noteuspto-grants-2012_06