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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 229067Erstellt: 24. Oktober 2026

Water → 3-(7-Benzyloxy-6-methoxy-quinolin-4-yloxy)-5,6,6'-trimethyl-[2,2']bipyridine

https://huagongshe.com/de/reaction/229067

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktCesium carbonateHCID 10796—
Edukt7-(Benzyloxy)-4-chloro-6-methoxyquinolineHCID 22646562—
Edukt5,6-Dimethyl-2-(6-methylpyridin-2-yl)pyridin-3-olHCID 136385107—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt3-(7-Benzyloxy-6-methoxy-quinolin-4-yloxy)-5,6,6'-trimethyl-[2,2']bipyridineHCID 5775654072,2%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

5,6,6′-Trimethyl-[2,2′]bipyridin-3-ol (300 mg), 7-benzyloxy-4-chloro-6-methoxyquinoline (1.26 g), 4-dimethylaminopyridine (513 mg), and cesium carbonate (1.37 g) were suspended in dimethyl sulfoxide (6 ml), and the suspension was stirred at 130° C. overnight. The reaction solution was cooled to room temperature, water was then added to the reaction solution, and the mixture was extracted with chloroform. The chloroform layer was washed with saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography using chloroform-methanol to give the title compound (483 mg, yield 72%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560558B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-146fedd606cf4b43b92bd93f65c0f8f9
Quellennotizuspto-grants-2009_07