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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44236Generated: October 25, 2026

Pyridine → N-(2-chloropyridin-3-yl)-5-methyl-2-nitrobenzamide

https://huagongshe.com/reaction/44236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Chloro-3-pyridylamineHCID 80528—
Reactant5-Methyl-2-nitrobenzoyl chlorideHCID 3016013—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductN-(2-chloropyridin-3-yl)-5-methyl-2-nitrobenzamideHCID 344016198.7%

Reaction Steps

A solution of 5-methyl-2-nitrobenzoyl chloride (3.77 g, 18.9 mmol) in tetrahydrofuran (25 mL) was treated with a solution consisting of 2-chloropyridin-3-amine (2.6 g, 20.22 mmol), pyridine (6 mL) and tetrahydrofuran (15 mL). The reaction mixture was stirred for 2 hours then diluted with water (150 mL) and extracted with dichloromethane (3×70 mL). The combined organic extracts were washed with saturated aqueous sodium bicarbonate (100 mL) and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford N-(2-chloropyridin-3-yl)-5-methyl-2-nitrobenzamide (5.44 g) that was used without further purification. LCMS [M+H]: 292.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541407B2
Source datasetuspto-grants-2013_09
ORD IDord-8de85d599504467eb920c5fc0f296886
Source noteuspto-grants-2013_09