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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1817447Erstellt: 26. Oktober 2026

Triethylamine → N-(2-Fluoro-4-{[6-methoxy-7-(3-morpholinopropoxy)-4-quinolyl]oxy}phenyl)-N'-[1-(4-fluorophenyl)ethyl]urea

https://huagongshe.com/reaction/1817447

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktTriphosgeneHCID 94429—
Edukt1-(4-Fluorophenyl)ethylamineHCID 123063—
Edukt2-Fluoro-4-{[6-methoxy-7-(3-morpholinopropoxy)-4-quinolyl]oxy}-anilineHCID 69057905—
LösungsmittelChloroformHCID 6212—
ProduktN-(2-Fluoro-4-{[6-methoxy-7-(3-morpholinopropoxy)-4-quinolyl]oxy}phenyl)-N'-[1-(4-fluorophenyl)ethyl]ureaHCID 1037122891,3%

Reaktionsschritte

2-Fluoro-4-{[6-methoxy-7-(3-morpholinopropoxy)-4-quinolyl]oxy}-aniline (30 mg) was dissolved in chloroform (3 ml) and triethylamine (0.3 ml) to prepare a solution. A solution of triphosgene (17 mg) in chloroform (0.2 ml) was then added to the solution, and the mixture was stirred at room temperature for 25 min. Next, a solution of 1-(4-fluorophenyl)ethylamine (12 mg) in chloroform (0.2 ml) was added thereto, and the mixture was stirred at room temperature for 5 hr. The stirred mixture was purified by chromatography on silica gel using chloroform/methanol for development to give the title compound (31 mg, yield 73%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07598258B2
Quelldatensatzuspto-grants-2009_10
ORD IDord-6dbb01ef414543efb6440c20d824a555
Quellennotizuspto-grants-2009_10