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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54662Generated: October 25, 2026

Benzoyl chloride → 2-Chloro-5-benzoylaminopyridine

https://huagongshe.com/reaction/54662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant5-(Aminomethyl)-2-chloropyridineHCID 7020927—
SolventDichloromethaneHCID 6344—
Product2-Chloro-5-benzoylaminopyridineHCID 9794648105.7%

Reaction Steps

14.25 g (0.1 mol) of 2-chloro-5-aminomethylpyridine and 11.1 g (0.11 mol) of triethylamine are dissolved in 150 ml of methylene chloride. 14.8 g (0.105 mol) of benzoyl chloride are then added dropwise at about 20° C. and the reaction mixture is subsequently stirred overnight at room temperature. It is washed three times with water and the organic phase is dried and concentrated. 24.6 g (99.8% of theory) of 2-chloro-5-benzoylaminopyridine are obtained as white crystals of melting point 118°-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05623076
Source datasetuspto-grants-1997_04
ORD IDord-f2161ce8085e4e71a9a2e8a6ca6c75aa
Source noteuspto-grants-1997_04