Reaktion #72871
ord-4469cbe0f5874bb0a1dfebaf757e02f6
Reaktionsgleichung
guanidine hydrochloride
ethyl-6-[(dimethylamino)methylene]-1-methyl-7-oxo-4,5,6,7-tetrahydro-1H-indazole-3-carboxylate
→
Ethyl 8-amino-1-methyl-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate
Ausbeute 85.0%
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Temperaturat reflux for 12 hours
- 2SonstigeThe solvent was then evaporated
- 3workup.DISSOLUTIONthe residue redissolved with dichloromethane
- 4Waschenwashed with water
- 5TrocknenThe organic layer was then dried over anhydrous Na2SO4
- 6Einengenconcentrated
- 7SonstigeThe residue was triturated with diethyl ether
- 8Filtrationthe product collected by filtration (85% yield as a white solid)
Vorschrift
16.00 g (0.06 mol) of ethyl-6-[(dimethylamino)methylene]-1-methyl-7-oxo-4,5,6,7-tetrahydro-1H-indazole-3-carboxylate were dissolved in 600 mL of ethanol and 3.90 g of sodium ethylate, and 5.44 g of guanidine hydrochloride were added consecutively. The solution was stirred at reflux for 12 hours. The solvent was then evaporated, the residue redissolved with dichloromethane and washed with water. The organic layer was then dried over anhydrous Na2SO4 and concentrated. The residue was triturated with diethyl ether and the product collected by filtration (85% yield as a white solid).