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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558087Generated: October 25, 2026

Pyridine → N-(5-chloropyridin-2-yl)-5-methyl-2-nitrobenzamide

https://huagongshe.com/reaction/558087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant5-Methyl-2-nitrobenzoic acidHCID 18371—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Amino-5-chloropyridineHCID 66174—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-(5-chloropyridin-2-yl)-5-methyl-2-nitrobenzamideHCID 356251992%

Reaction Steps

To a solution of 5-methyl-2-nitrobenzoic acid (1 g, 5.52 mmol) in dichloromethane (5 ml) was added oxalyl chloride (0.964 ml, 11.04 mmol) and a few drops of dimethylformamide. The mixture was stirred at r.t. for 2 hrs. After the evaporation of the solvent, the residue was dissolved in dichloromethane (5 ml). 2-amino-5-chloropyridine (852 mg, 6.62 mmol) and pyridine (1.34 ml, 16.56 mmol) were added to the solution. The mixture was stirred at r.t. overnight. After the evaporation of the solvent, the crude residue was purified by silica gel column chromatography using solvent system 25% ethyl acetate in hexane as eluent to give N-(5-chloro(2-pyridyl))(5-methyl-2-nitrophenyl)carboxamide as a solid (1.48 g, 92%). MS found for C13H10ClN3O3 M+=291, (M+2)+=293.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063036B2
Source datasetuspto-grants-2011_11
ORD IDord-437ed4bcee65435da24a2a9b3b30efd1
Source noteuspto-grants-2011_11