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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 988608Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/988608

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Phenylbenzoyl chlorideHCID 84151—
Edukt2-amino-N-(5-chloropyridin-2-yl)benzamideHCID 21906381—
LösungsmittelPyridineHCID 1049—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(5-Chloropyridin-2-yl)-2-(4-phenylbenzoylamino)benzamideHCID 2190658794%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06635657B1
Quelldatensatzuspto-grants-2003_10
ORD IDord-c097e432feb545178e2ce278c61c05b1
Quellennotizuspto-grants-2003_10