Reaktion #951935
ord-c5842266d2e945e983330692d24f918e
Reaktionsgleichung
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturwas slowly warmed to room temperature
- 2workup.ADDITIONThe mixture was poured
- 3Sonstigeupon evaporation of the dry ice the solvent
- 4Sonstigewas removed in vacuo
- 5Extraktionextracted with chloroform (2X)
- 6SonstigeThe organic layer was separated
- 7Einengenconcentrated in vacuo
- 8Sonstigeto afford 6.0 g
- 9Sonstigeof recovered
- 10EinengenThe aqueous layer was concentrated in vacuo and 3N HCl
- 11workup.ADDITIONwas added to the residue
- 12TemperaturThe 15 solution was cooled
- 13Sonstigea solid was obtained which
- 14Filtrationwas collected by filtration
- 15SonstigeThe solid was recrystallized from water
Vorschrift
A solution of lithium diisopropylamide (6.4 g, 0.06 mol) in THF (100 ml) under nitrogen was cooled to -70° C. and a solution of 3, 5-dichloro-2-[2-(4-morpholinyl) ethoxy]pyridine (13.0 g, 0.047 mol) in THF (10 ml) was added via syringe. The yellow/red solution was stirred for 30 minutes at -70° C. and then was slowly warmed to room temperature. The mixture was poured onto crushed dry ice/THF and upon evaporation of the dry ice the solvent was removed in vacuo. The residue was taken up in dilute ammonium hydroxide and extracted with chloroform (2X). The organic layer was separated and concentrated in vacuo to afford 6.0 g of recovered starting material. The aqueous layer was concentrated in vacuo and 3N HCl was added to the residue. The 15 solution was cooled and a solid was obtained which was collected by filtration. The solid was recrystallized from water to afford 3,5-dichloro-2-[2-(4-morpholinyl)ethoxy]pyridine-4-carboxylic acid hydrochloride as a white solid in 71% yield (based on recovered starting material), m.p. 230°-231° C. (dec.).