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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 514736Erstellt: 24. Oktober 2026

Pyridine → n-{4-Chloro-2-[n-(5-chloro(2-pyridyl))carbamoyl]phenyl}(2-fluoro-4-cyanophenyl)carboxamide

https://huagongshe.com/de/reaction/514736

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukt4-Cyano-2-fluorobenzoic acidHCID 590659—
Edukt2-Amino-5-chloro-N-(5-chloropyridin-2-yl)benzamideHCID 21906418—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelThionyl ChlorideHCID 24386—
Produktn-{4-Chloro-2-[n-(5-chloro(2-pyridyl))carbamoyl]phenyl}(2-fluoro-4-cyanophenyl)carboxamideHCID 10181017111,3%

Reaktionsschritte

A solution of 2-fluoro-4-cyanobenzoic acid (1 g, 6.06 mmol) in thionyl chloride (5 ml) was refluxed for 2 hr. After concentration, the residue was dissolved in dichloromethane (5 ml). And a solution of the compound of (2-amino-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide (1.2 g, 4.25 mmol) in dichloromethane (10 ml) and pyridine (1.47 ml, 18.18 mmol) were added. The mixture was stirred at r.t. overnight. The precipitate was filtered and washed with a little amount of dichloromethane to give N-{4-chloro-2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}(2-fluoro-4-cyanophenyl)carboxamide (2.03 g, 78%). MS found for C20H11Cl2FN4O2 M+=429, (M+2)+=431.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09108922B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-641c9a6b3268425bac5bb73a32221841
Quellennotizuspto-grants-2015_08