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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370571Generated: October 31, 2026

Methylamine → 4-chloro-N-methylpyridine-3-carboxamide

https://huagongshe.com/reaction/2370571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant4-Chloronicotinoyl chloride hydrochlorideHCID 23152008—
SolventTetrahydrofuranHCID 8028—
Product4-chloro-N-methylpyridine-3-carboxamideHCID 2266392924%

Reaction Steps

To a suspension of crude 4-chloronicotinoyl chloride hydrochloride in 25 mL of THF was added methylamine solution (2M in THF, 20 mL, 40 mmol, 4.0 eq) at 0° C. The reaction mixture was stirred at room temperature for 1 hour and concentrated under reduced pressure. The crude material was dissolved in ethylacetate (75 mL) and water/brine/saturated sodium bicarbonate solution (1/1/1, 75 mL). The separated aqueous layer was extracted with EtOAc. The combined organic layers were washed with water/brine/saturated sodium bicarbonate solution (1/1/1, 25 mL) and brine (25 mL) and dried over sodium sulfate. Removal of the solvent under reduced pressure afforded the title compound as orange solid (400 mg, 24%), which was used without further purification. MH+=171.0, Rt=0.55 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710048B2
Source datasetuspto-grants-2014_04
ORD IDord-fc3c852e39654da086ec0d15afd3286d
Source noteuspto-grants-2014_04