Reaktion #68224
ord-b40e19f5a5bf46daa1293b79357c9df7
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1workup.ADDITIONwere added
- 2workup.ADDITIONwere added
- 3Sonstigethe organic layer was separated
- 4Extraktionthe aqueous layer was extracted with ethyl acetate
- 5Waschenwashed with aqueous saturated sodium chloride solution
- 6Trocknendried over anhydrous magnesium sulfate
- 7Sonstigethe solvent was removed under reduced pressure
- 8SonstigeThe residue thus obtained
- 9Sonstigewas purified by silica gel column chromatography [eluent; chloroform:methanol=10:1]
Vorschrift
To 2 mL of an N,N-dimethylformamide solution containing 0.14 g of tert-butyl (2,3-dihydro-1,4-benzodioxin-6-ylmethyl)(1-(2-(4-(trifluoromethanesulfonyl)oxy-2-oxoquinolin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate, 0.24 mL of 2.0 mol/L aqueous sodium carbonate solution, 12 mg of tetrakis triphenylphosphine palladium and 39 mg of 4-pyridineboronic acid were added, and stirred at 120° C. under nitrogen atmosphere for 80 min. The reaction mixture was cooled to the room temperature, ethyl acetate and water were added, the organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and extracts were combined, washed with aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent; chloroform:methanol=10:1], to give 42 mg of tert-butyl (2,3-dihydro-1,4-benzodioxin-6-ylmethyl)(1-(2-(2-oxo-4-(pyridin-4-yl)quinolin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate as a pale yellow solid.