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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44243Generated: October 25, 2026

Triethylamine → N-(5-bromo-2-chloropyridin-3-yl)-2-nitrobenzamide

https://huagongshe.com/reaction/44243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Nitrobenzoyl chlorideHCID 11875—
Reactant3-Amino-5-bromo-2-chloropyridineHCID 21858354—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
ProductN-(5-bromo-2-chloropyridin-3-yl)-2-nitrobenzamideHCID 86658034—

Reaction Steps

To a solution of 5-bromo-2-chloropyridine-3-amine (3.9 g, 18.9 mmol) and triethylamine (5.3 mL, 37.9 mmol) in tetrahydrofuran (60 mL) was added 2-nitrobenzoylchloride (2.49 mL, 18.9 mmol). The reaction was stirred for 24 hours. The reaction mixture was diluted with ethyl acetate (200 mL) and saturated aqueous sodium bicarbonate (60 mL). The organic layer was separated and washed with water (50 mL), brine (50 mL), dried over sodium sulfate, filtered and concentrated to dryness under reduced pressure. The crude product was purified by flash chromatography (SiO2, 25% ethyl acetate in hexanes). The N-(5-bromo-2-chloropyridin-3-yl)-2-nitrobenzamide was obtained as a yellow solid (1.5 g). LCMS [M+H]: 356.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541407B2
Source datasetuspto-grants-2013_09
ORD IDord-ab89fc2dc2b24ffea8f46cdcfcbc29fa
Source noteuspto-grants-2013_09