Reaktionsgleichung
F[C:2]1[CH:9]=[CH:8][C:7]([C:10]([F:13])([F:12])[F:11])=[CH:6][C:3]=1[C:4]#[N:5].[NH2:14][NH2:15].O>CCCCO>[F:11][C:10]([F:12])([F:13])[C:7]1[CH:6]=[C:3]2[C:2](=[CH:9][CH:8]=1)[NH:15][N:14]=[C:4]2[NH2:5]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2-Fluoro-5-trifluoromethyl-benzonitrile (2.66 g) was dissolved in n-BuOH (51 ml) prior to the addition of NH2NH2.H2O (1.02 ml). The solution was heated to reflux for 30 min. After cooling to rt, the solution was concentrated and CH2Cl2 was added. The organic layer was washed with H2O, brine, dried, filtered, and concentrated in high vacuum to give 5-trifluoromethyl-1H-indazol-3-ylamine (2.25 g): 1H NMR (DMSO, δppm, 300 mHz) 5.70 (s, br, 2H), 7.40 (dd, 2H), 8.20 (s, 1H), 11.90 (s, br, 1H).
Aufarbeitung
- temperatureThe solution was heated
- temperatureto reflux for 30 min
- concentrationthe solution was concentrated
- additionCH2Cl2 was added
- washThe organic layer was washed with H2O, brine
- customdried
- filtrationfiltered
- concentrationconcentrated in high vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-958bd81a35f8429eb342cc6ebbb51120
- Quelldatensatz
- uspto-grants-2010_08
- Patentnummer
- US07776884B2
Verknüpfte Notizen
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