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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988608Generated: October 25, 2026

4-Phenylbenzoyl chloride → N-(5-Chloropyridin-2-yl)-2-(4-phenylbenzoylamino)benzamide

https://huagongshe.com/reaction/988608

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenylbenzoyl chlorideHCID 84151—
Reactant2-amino-N-(5-chloropyridin-2-yl)benzamideHCID 21906381—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductN-(5-Chloropyridin-2-yl)-2-(4-phenylbenzoylamino)benzamideHCID 2190658794%

Reaction Steps

To a solution of N-(5-chloropyridin-2-yl)-2-aminobenzamide(0.247 g, 1 mmol) in dichloromethane (10 mL) and pyridine (0.5 mL) was added a solution of 4-biphenylcarbonyl chloride (0.217 g, 1 mmol) in dichloromethane (5 mL). After stirring overnight the solvent was removed in vacuo. The residue was partitioned between ethyl acetate (50 mL) and water (25 mL). Separate the layers and wash the organic layer with water (2×10 mL), saturated sodium bicarbonate (2×20 mL), hydrochloric acid (0.2 N, 1×20 mL). Dried over MgSO4, filtered and concentrated in vacuo. The residue was then purified by RPHPLC (30% ethyl acetate/hexane) to give 0.4 g (94%) of pure product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06635657B1
Source datasetuspto-grants-2003_10
ORD IDord-c097e432feb545178e2ce278c61c05b1
Source noteuspto-grants-2003_10