Reaktion #43742
ord-bb2b1acbb9aa4d18911994645d145dcd
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1SonstigeDMF is removed under reduced pressure
- 2workup.DISSOLUTIONthe crude product is dissolved in 1N aqueous sodium hydroxide solution
- 3ExtraktionThe aqueous phase is extracted with ethyl acetate
- 4TrocknenThe combined organic phases are dried over magnesium sulfate
- 5Sonstigethe solvent is removed under reduced pressure
- 6Sonstigea rotary evaporator
- 7WaschenThe loaded ion exchanger is washed three times with in each case 30 ml of methanol
- 8WaschenThe product is eluted with methanol/triethylamine 95:5
- 9SonstigeThe solvent is removed under reduced pressure
- 10Sonstigea rotary evaporator
Vorschrift
55 mg (0.28 mmol) of 5,7-difluoro-1-benzofuran-2-carboxylic acid, 50 mg (0.25 mmol) of (R)-3-aminoquinuclidine dihydrochloride, 114.6 mg (0.3 mmol) of HATU, 117 mg (0.9 mmol) of N,N-diisopropylethylamine and 2.0 ml of DMF are reacted according to the general procedure (variant B). DMF is removed under reduced pressure and the crude product is dissolved in 1N aqueous sodium hydroxide solution. The aqueous phase is extracted with ethyl acetate. The combined organic phases are dried over magnesium sulfate and the solvent is removed under reduced pressure using a rotary evaporator. The crude product is taken up in methanol and, together with acidic ion exchange resin (Dowex WX2-200), shaken for about 20 min. The loaded ion exchanger is washed three times with in each case 30 ml of methanol, then with water, again with methanol, with dichloromethane and finally again with methanol. The product is eluted with methanol/triethylamine 95:5. The solvent is removed under reduced pressure using a rotary evaporator. 40 mg (52% of theory) of the title compound are isolated.