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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247020Generated: October 31, 2026

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

https://huagongshe.com/reaction/1247020

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) and pyridine (7.3 mL, 90 mmol) in dichloromethane (200 mL) was added 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 again with water (250 mL) followed by brine (250 mL) and then dried with MgSO4, filtered and partially concentrated in vacuo, which resulted in the formation of a precipitate. After standing overnight, the solid was filtered and dried in vacuo to give 3.9 g (52%) of white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129245B2
Source datasetuspto-grants-2006_10
ORD IDord-a50834942f344c55aec43e7eafdce93f
Source noteuspto-grants-2006_10