Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333978Generated: October 30, 2026

Triethylamine → 4-Chloro-N-methylpicolinamide

https://huagongshe.com/reaction/333978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethylamine hydrochlorideHCID 6364545—
Reactant4-chloropyridine-2-carbonyl ChlorideHCID 11095146—
SolventDichloromethaneHCID 6344—
Product4-Chloro-N-methylpicolinamideHCID 147681452.4%

Reaction Steps

To a solution of methylamine hydrochloride (2.057 g, 30.5 mmol) and triethylamine (14.16 ml, 102 mmol) in DCM (30 ml) at 0° C., was added 4-chloropyridine-2-carbonyl chloride (3.575 g, 20.31 mmol) in DCM (20 ml). The resulting black suspension was allowed to reach room temperature and stirred overnight. The mixture was concentrated under reduced pressure and dissolved in ethyl acetate. Water was added and the layers were separated. The aqueous layer was extracted with ethyl acetate (3×), the combined organic layers were washed with water (3×) and brine, dried with Na2SO4 and concentrated under reduced pressure. The residue was purified with column chromatography (20-50% ethyl acetate in n-heptane) to give 2.04 gram of a yellow oil (10.64 mmol, 52%). MS (ESI) m/z=170.0 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883791B2
Source datasetuspto-grants-2014_11
ORD IDord-c01a2569c4454daeb1754f553090b0c5
Source noteuspto-grants-2014_11