Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164950Generated: October 29, 2026

Triethylamine → 2,N-Dimethyl-N-(3-methyl-4-nitrophenyl)pyridine-4-carboxamide

https://huagongshe.com/reaction/1164950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Methyl-4-pyridinecarbonyl chlorideHCID 11788423—
ReactantN,3-Dimethyl-4-nitroanilineHCID 14146034—
SolventDichloromethaneHCID 6344—
Product2,N-Dimethyl-N-(3-methyl-4-nitrophenyl)pyridine-4-carboxamideHCID 19863463—

Reaction Steps

To a solution of 16.6 g (0.1 mol) of 3,N-dimethyl-4-nitrobenzenamine and 10.2 g (0.1 mol) of triethylamine in mL of methylene chloride cooled to 0° C. under a nitrogen atmosphere add slowly a solution of 15.6 g (0.1 mol) of 2-methylpyridine-4-carbonyl chloride (prepared from the corresponding acid and thionyl chloride) such that the temperature is maintained between 0°-5° C. After the addition is complete, stir the mixture for 6 h and allow to warm slowly to room temperature. Quench the reaction mixture by the addition of 50 mL of water. Separate the layers and wash the organic layer with two 50 mL portions of water, two 50 mL portions of 5% sodium bicarbonate solution and 50 mL of saturated sodium chloride solution. Dry the methylene chloride solution over anhydrous sodium sulfate. Remove the drying agent by filtration and evaporate the solvent to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906634
Source datasetuspto-grants-1990_03
ORD IDord-9e770a796a1a40d183e65ca7df663776
Source noteuspto-grants-1990_03