Reaktion #343367
ord-58c263adda3e48148f252143a817e691
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Filtrationthe mixture was filtered through kieselguhr
- 2Sonstigethe solvent evaporated
- 3workup.ADDITIONthe residue diluted with 50% methanol/ether ether (500 mL)
- 4SonstigeA light spray powder (25.0 g) was collected in two crops
- 5workup.ADDITIONThe powder was added to methanol (500 mL)
- 6workup.ADDITIONcontaining p-toluene sulfonic acid (1.5 g)
- 7Temperaturheated
- 8Temperaturat reflux for 18 hours
- 9TemperaturUpon cooling
- 10Filtrationthe mixture was filtered
- 11Sonstigeto give 19.5 g of an off white solid
Vorschrift
Ethyl 1-[3-[(2,4-dioxoimidazolidin-5-ylidene)methyl]-4-nitrophenyl]-4-piperidinecarboxylate (35.8 g, 92 mmol) in dimethylformamide (500 mL) was hydrogenated over 10% palladium on charcoal (3.6 g) at 200 psi pressure. After 42 hours, the mixture was filtered through kieselguhr, the solvent evaporated, and the residue diluted with 50% methanol/ether ether (500 mL). A light spray powder (25.0 g) was collected in two crops. The powder was added to methanol (500 mL) containing p-toluene sulfonic acid (1.5 g), and heated at reflux for 18 hours. Upon cooling, the mixture was filtered to give 19.5 g of an off white solid consisting of a mixture of ethyl 1-(1,3,9,9a-tetrahydro-2-oxo-1H-imidazo[4,5-b]quinolin-7-yl)-4-piperidinecarboxylate and the corresponding oxidized 2,3-dihydro compound (ethyl ester of the title compound). The solid was added to methanol (500 mL), heated to reflux, iodine (13.7 g, 54 mmol) added portionwise, and reflux continued for 2.5 hours. Upon cooling, 10% sodium thiosulfate and 10% sodium carbonate solution were added until pH=7. Water (300 mL) was added, and the precipitate consisting of the title compound collected (19.4 g, 65%).