Reaktionsgleichung
[NH2:1][NH2:2].[Br:3][C:4]1[CH:5]=[N:6][C:7](OC)=[C:8]([CH:11]=1)[C:9]#[N:10]>>[Br:3][C:4]1[CH:11]=[C:8]2[C:9]([NH2:10])=[N:2][NH:1][C:7]2=[N:6][CH:5]=1Komponenten
3
Versuchsvorschrift
35 ml (23.47 mmol) of hydrazine is added at room temperature to 5 g (23.47 mmol) of 5-bromo-2-methoxynicotinonitrile. The reaction medium is carried at 100° C. for 3 hours. After returning to room temperature, the precipitate obtained is filtered, rinsed with water and then dried at 50° C. to yield 3.6 g (72%) of 5-bromo-1H-pyrazolo[3,4-b]pyridine-3-amine in the form of a yellow solid.
Aufarbeitung
- customAfter returning to room temperature
- customthe precipitate obtained
- filtrationis filtered
- washrinsed with water
- customdried at 50° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-0169b87339f84558bb73083e1a75dc0a
- Quelldatensatz
- uspto-grants-2014_11
- Patentnummer
- US08883821B2
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