Reaktion #316251

Reaktionsgleichung

4-(5,6-Dimethyl-[2,3′]bipyridin-3-yloxy)-6-methoxy-quinolin-7-ol

compound 345

4-(5,6-Dimethyl-[2,3′]bipyridin-3-yloxy)-6-methoxy-quinolin-7-ol

Potassium carbonate

4-bromo-1-butanol

Water

→

title compound

Ausbeute 35.4%

4-[4-(5,6-Dimethyl-[2,3′]bipyridin-3-yloxy)-6-methoxy-quinolin-7-yloxy]-butan-1-ol

Ausbeute 35.4%

Lösungsmittel

N,N-dimethylformamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigeto prepare a solution
2. 2
   Extraktionthe mixture was extracted with ethyl acetate
3. 3
   Waschenthe ethyl acetate layer was then washed with saturated brine
4. 4
   Trocknenwas dried over anhydrous sodium sulfate
5. 5
   SonstigeThe solvent was removed by distillation under the reduced pressure
6. 6
   Sonstigethe residue was purified by thin layer chromatography

Vorschrift

4-(5,6-Dimethyl-[2,3′]bipyridin-3-yloxy)-6-methoxy-quinolin-7-ol (compound 345) (45 mg) was dissolved in N,N-dimethylformamide (2 ml) to prepare a solution. Potassium carbonate (50 mg) and 4-bromo-1-butanol (55 mg) were added to the solution, and the mixture was stirred at room temperature overnight. Water was added to the reaction solution, the mixture was extracted with ethyl acetate, and the ethyl acetate layer was then 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 thin layer chromatography using chloroform-acetone to give the title compound (19 mg, yield 35%).

Quelle