Ammonia → 5-Amino-1-cyclohexyl-1H-pyrazole-4-carboxamide
Reaktionsgleichung
[OH:1]O.[NH2:3][C:4]1[N:8]([CH:9]2[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]2)[N:7]=[CH:6][C:5]=1[C:15]#[N:16].N>C(O)C>[NH2:3][C:4]1[N:8]([CH:9]2[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]2)[N:7]=[CH:6][C:5]=1[C:15]([NH2:16])=[O:1]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
18 ml of 30% strength hydrogen peroxide solution are added to a solution of 5-amino-1-cyclohexyl-1H-pyrazole-4-carbonitrile (1.86 g, 9.81 mmol) in a mixture of 73 mi of ethanol and 90 ml of concentrated aqueous ammonia solution at room temperature, and the mixture is stirred at room temperature for 1 h. The nonaqueous solvents are then stripped off in a rotary evaporator. The product precipitates as solids from the remaining mixture and is filtered off with suction, washed with a little water and dried under high vacuum.
Aufarbeitung
- customThe nonaqueous solvents are then stripped off in a rotary evaporator
- customThe product precipitates as solids from the remaining mixture
- filtrationis filtered off with suction
- washwashed with a little water
- customdried under high vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-0d654b4eaef941f9b8fe299bda33ca75
- Quelldatensatz
- uspto-grants-2014_06
- Patentnummer
- US08741907B2
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