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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842835Generated: October 25, 2026

Pyridine → n-(5-Bromo(2-pyridyl))(3,4,5-trimethoxy-2-nitrophenyl)carboxamide

https://huagongshe.com/reaction/842835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Amino-5-bromopyridineHCID 70622—
Reactant3,4,5-Trimethoxy-2-nitrobenzoic acidHCID 97116—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Productn-(5-Bromo(2-pyridyl))(3,4,5-trimethoxy-2-nitrophenyl)carboxamideHCID 2259631998.3%

Reaction Steps

To a solution of 3,4,5-trimethoxy-2-nitrobenzoic acid (0.5 g, 1.95 mmol) in dichloromethane (5 ml) was added oxalyl chloride (0.34 ml, 3.9 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-bromopyridine (0.81 g, 4.7 mmol) and pyridine (0.94 ml, 11.7 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-bromo(2-pyridyl))(3,4,5-trimethoxy-2-nitrophenyl)carboxamide as a solid (790 mg, 98%). MS found for C15H14BrN3O6 M+=412, (M+2)+=414.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376515B2
Source datasetuspto-grants-2002_04
ORD IDord-4bbabe1203cd40e88fe4c47e998ebc99
Source noteuspto-grants-2002_04