Reaktion #2027193
ord-31149e0d3d5c4dc7928557d770e8d47e
Reaktionsgleichung
2-(4-t-butoxycarbonylaminophenyl)-3-oxobutyronitrile
ethanol
2,2-diethoxyethylhydrazine
hydrogen chloride
→
title compound
7-(4-Aminophenyl)-6-methyl-1H-imidazo[1,2-b]pyrazole Hydrochloride
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Temperaturwas heated
- 2Temperaturunder reflux for 2 hours
- 3Temperaturthe whole mixture was heated
- 4Temperaturunder reflux for a further 30 minutes
- 5TemperaturAfter the mixture had been cooled
- 6Sonstigeto precipitate crystals
- 7FiltrationThese crystals were collected by filtration
- 8Sonstigerecrystallized from ethanol
Vorschrift
A mixture of 2.5 g of 2-(4-t-butoxycarbonylaminophenyl)-3-oxobutyronitrile, 20 ml of ethanol and 1.4 g of 2,2-diethoxyethylhydrazine was heated under reflux for 2 hours. 20 ml of 4N hydrogen chloride in dioxane were added, and then the whole mixture was heated under reflux for a further 30 minutes. After the mixture had been cooled, ethyl acetate was added to precipitate crystals. These crystals were collected by filtration and recrystallized from ethanol to give 1.4 g of the title compound as pale brown plates melting at 180°-190° C.