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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883044Generated: November 1, 2026

Pyridine → HCID 16731657, compound

https://huagongshe.com/reaction/1883044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Amino-5-chloropyridineHCID 66174—
Reactant3-Methoxy-2-nitrobenzoic acidHCID 78632—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 16731657HCID 1673165779%

Reaction Steps

To a stirring suspension of 3-methoxy-2-nitrobenzoic acid (14.5 g, 73.5 mmol) in dichloromethane (100 mL) was added a couple of drops of N,N-dimethylformamide followed by oxalyl chloride (6.7 mL, 77.1 mmol). The reaction was stirred at room temperature overnight and the residue transferred slowly to an ice cold solution of 2-amino-5-chloropyridine (9 g, 70 mmol) and pyridine (20 mL) in dichloromethane (200 mL). The reaction was stirred overnight, treated with water, and concentrated. The resulting mixture was treated with ethyl acetate, washed consecutively with aqueous citric acid, saturated aqueous sodium bicarbonate, dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude product was purified by recrystallization from toluene to give 17 g (79%) of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06759414B2
Source datasetuspto-grants-2004_07
ORD IDord-c6d29a0433fa49ed9e271fdac639426c
Source noteuspto-grants-2004_07