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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895290Generated: October 30, 2026

Potassium Carbonate → 2-(methylamino)pyridine-3-carboxylic acid

https://huagongshe.com/reaction/895290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloronicotinic acidHCID 76258—
ReactantMethylamine hydrochlorideHCID 6364545—
Catalystcopper(I) bromideHCID 24593—
SolventDimethylformamideHCID 6228—
Product2-(methylamino)pyridine-3-carboxylic acidHCID 4738517—

Reaction Conditions

Temperature100 °C

Reaction Steps

Methylamine hydrochloride (8.6 g, 128 mmol) was added portionwise to a mixture of 2-chloronicotinic acid (10.0 g, 64 mmol), potassium carbonate (35.4 g, 256 mmol) and copper (I) bromide (920 mg, 6.4 mmol) in N,N-dimethylformamide (100 ml), and the reaction heated at 100° C. for 18 hours, then cooled. The resulting precipitate was removed by filtration, washing through with additional methanol and the filtrate evaporated under reduced pressure. The residue was redissolved in 2N sodium hydroxide solution (200 ml), washed with diethyl ether (4×80 ml), then the pH of the aqueous solution adjusted to 6, using concentrated hydrochloric acid. This aqueous solution was evaporated under reduced pressure, the residue dissolved in methanol, poly(4-vinylpyridine), 2% cross-linked (5 g) was added, and the mixture stirred at room temperature for 18 hours. The resin was removed by filtration, and the procedure then repeated. The solution was evaporated under reduced pressure, and the solid recrystallised from ethanol, to afford the title compound, 5.2 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06914160B1
Source datasetuspto-grants-2005_07
ORD IDord-f62e92424b8d45ffb826e7278bd7e8c0
Source noteuspto-grants-2005_07