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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 868214Erstellt: 26. Oktober 2026

Pyridine → N-[[[1-(6-Fluoro-2-naphthalenylmethyl)-4-piperidinyl]amino]carbonyl]-6-quinoline carboxamide

https://huagongshe.com/reaction/868214

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktQuinoline-6-carbonyl chlorideHCID 12391963—
EduktN-[[(6-fluoro-2-naphthalenyl)methyl]-4-piperidinyl]ureaHCID 21288076—
Lösungsmittel1,2-DichloroethaneHCID 11—
ProduktN-[[[1-(6-Fluoro-2-naphthalenylmethyl)-4-piperidinyl]amino]carbonyl]-6-quinoline carboxamideHCID 13853618—

Reaktionsschritte

A mixture of 6-quinolinoyl chloride (4.77 g, 22 mmol), N-[[(6-fluoro-2-naphthalenyl)methyl]-4-piperidinyl]urea (6.02 g, 20 mmol), dry pyridine (2.5 ml) and 1,2-dichloroethane (30 ml) is stirred at reflux for 18 hours. The solution is then cooled, washed with aqueous sodium carbonate solution, dried and evaporated. The residue is crystallised from ethanol to give the title compound, mp 200°-201° C. (softens, maleate salt).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04778802
Quelldatensatzuspto-grants-1988_10
ORD IDord-fe4ffe43b4e3413780803c628c8a457f
Quellennotizuspto-grants-1988_10