Reaktion #618274
ord-a34d36904515466a81a531ed91799cee
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1workup.STIRRINGThe mixture was stirred at the same temperature under nitrogen atmosphere for 16 hours
- 2SonstigeThe mixture was quenched with saturated sodium hydrogen carbonate aqueous solution at room temperature
- 3Extraktionextracted with ethyl acetate
- 4SonstigeThe organic layer was separated
- 5Waschenwashed with water and brine
- 6Trocknendried over anhydrous magnesium sulfate
- 7Einengenconcentrated in vacuo
- 8SonstigeThe residue was purified by a silica gel column chromatography (hexane/ethyl acetate
Vorschrift
Triethylamine (3.26 g) was added to a mixture of ethyl 5-oxo-6-(piperidin-4-yl)-2-propyl-5,6,7,8-tetrahydro-1,6-naphthyridine-3-carboxylate dihydrochloride monohydrate (5.92 g) and 6-cyclopropyl-3-ethoxy-2,4′-difluorobiphenyl-4-carbaldehyde (5.35 g) in THF (100 mL) at room temperature. The mixture was stirred at the same temperature under nitrogen atmosphere for 10 minutes. Sodium triacetoxyhydroborate (6.82 g) was added to the reaction mixture at room temperature. The mixture was stirred at the same temperature under nitrogen atmosphere for 16 hours. The mixture was quenched with saturated sodium hydrogen carbonate aqueous solution at room temperature and extracted with ethyl acetate. The organic layer was separated, washed with water and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was purified by a silica gel column chromatography (hexane/ethyl acetate then NH silica gel, hexane/ethyl acetate) to give the title compound (7.98 g)