Reaktion #79765
ord-1a8edf61788143b88d2c5384b5067193
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Filtrationthe mixture was filtered through an EMPORE® cartridge
- 2SonstigeThe filtrate was evaporated
- 3workup.DISSOLUTIONthe residue was dissolved in dichloromethane (5 ml)
- 4workup.ADDITIONwere added
- 5workup.STIRRINGthe mixture was stirred at ambient temperature overnight
- 6SonstigeThe polymer was removed by filtration
- 7Waschenwashed with dichloromethane
- 8SonstigeThe combined organic filtrate and washings were evaporated under reduced pressure
- 9Sonstigeto give an oil which
- 10Sonstigewas triturated with diethyl ether/ethyl acetate
- 11Temperaturwith warming
- 12workup.DISSOLUTIONto dissolve the solid
- 13Temperaturthe solution was cooled in ice
- 14Filtrationfiltered
Vorschrift
A mixture of 2-[4-(4-amino-7-(3-tetrahydrofuryl)-7H-pyrrolo[2,3-d)pyrimidin-5-yl)phenoxy]benzaldehyde (0.15 g), morpholine (64 mg), sodium triacetoxyborohydride (117 mg) and 1,2 dichloroethane (5 ml) was stirred at ambient temperature for 18 hours. Saturated aqueous sodium bicarbonate solution was added and the mixture was filtered through an EMPORE® cartridge. The filtrate was evaporated and the residue was dissolved in dichloromethane (5 ml) and then tris(2-aminoethyl)amine-polymer bound (0.3 g) and 2 drops of glacial acetic acid were added and the mixture was stirred at ambient temperature overnight. The polymer was removed by filtration and washed with dichloromethane and then with methanol. The combined organic filtrate and washings were evaporated under reduced pressure to give an oil which was triturated with diethyl ether/ethyl acetate with warming to dissolve the solid and then the solution was cooled in ice and filtered to give 5-[4-(2-morpholinomethylphenoxy)phenyl] -7-(3-tetrahydrofuryl)-7H-pyrrolo[2,3-d]pyrimidin-4-ylamine, m.p. 169-171° C.