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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269722Generated: November 1, 2026

Pyridine → N-(5-methylpyridin-2-yl)-2-nitrobenzamide

https://huagongshe.com/reaction/269722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Nitrobenzoyl chlorideHCID 11875—
Reactant2-Amino-5-methylpyridineHCID 15348—
SolventDichloromethaneHCID 6344—
ProductN-(5-methylpyridin-2-yl)-2-nitrobenzamideHCID 84032052.3%

Reaction Steps

To a stirring solution of 2-amino-5-methylpyridine (3.1 g, 29 mmol) in dichloromethane (200 mL) was added pyridine (7.3 mL, 90 mmol) followed by 2-nitrobenzoyl chloride (5.7 g, 30 mmol). After 4 h, the solvent was removed in vacuo and the residue was partitioned between ethyl acetate (500 mL) and water (250 mL). The organic phase was separated and washed with water, brine, dried (MgSO4) and filtered, and then concentrated in vacuo to a volume of about 100 mL (precipitate observed). The mixture was then sonicated and allowed to stand overnight then filtered. The collected solid was then washed with diethyl ether, filtered and dried under vacuum to give 3.9 g (52%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449457B2
Source datasetuspto-grants-2008_11
ORD IDord-5d926ab8217a4626b66edd9e0faf98cb
Source noteuspto-grants-2008_11