1-Methyl-2-[(2,4,6-trifluorophenyl)methylidene]hydrazine → 4,6-Difluoro-1-methyl-1H-indazole
Reaktionsgleichung
[CH3:1][NH:2]/[N:3]=[CH:4]/[C:5]1[C:10](F)=[CH:9][C:8]([F:12])=[CH:7][C:6]=1[F:13]>C(Cl)Cl>[F:13][C:6]1[CH:7]=[C:8]([F:12])[CH:9]=[C:10]2[C:5]=1[CH:4]=[N:3][N:2]2[CH3:1]Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
N-Methyl-N′-[1-(2,4,6-trifluoro-phenyl)-meth-(E)-ylidene]-hydrazine (3.85 g, 20.46 mmol) was heated in a seal tube at 210° C. for 2 hours. After cooled to room temperature, the black residue was dissolved in DCM and purified on flash chromatography (EtOAc:Hexane 10:90) to give the title compound as a light yellow crystal (1.926 g, 56%). 1H-NMR (400 MHz, MeOH-d4) δ ppm 8.05 (s, 1H); 7.16 (d, 1H); 6.75 (t, 1H); 3.32 (s, 3H). LCMS (method B): [MH]+=169, tR=2.28 min.
Aufarbeitung
- custompurified on flash chromatography (EtOAc:Hexane 10:90)
Quellen und Nachweise
- ORD-Eintrag
- ord-df1871ef2be0454dbd4ea08b483d08b3
- Quelldatensatz
- uspto-grants-2013_07
- Patentnummer
- US08497368B2
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