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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372869Generated: October 31, 2026

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

https://huagongshe.com/reaction/1372869

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 numberUS07160878B2
Source datasetuspto-grants-2007_01
ORD IDord-29acaf0089c14269849bb2a6e3953dde
Source noteuspto-grants-2007_01