Reaktionsgleichung
[CH2:1]([C:3]1[C:11]2[C:6](=[CH:7][C:8]([NH2:12])=[CH:9][CH:10]=2)[N:5]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[N:4]=1)[CH3:2].[ClH:19].CCOC(C)=O>>[ClH:19].[CH2:1]([C:3]1[C:11]2[C:6](=[CH:7][C:8]([NH2:12])=[CH:9][CH:10]=2)[N:5]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[N:4]=1)[CH3:2]Komponenten
3
Versuchsvorschrift
Into a 100-mL round-bottom flask, was placed 3-ethyl-1-phenyl-1H-indazol-6-amine (190 mg, 0.80 mmol, 1.00 equiv), hydrogen chloride/EtOAc (30 mL). The resulting solution was stirred for 30 min at room temperature. The resulting mixture was concentrated under vacuum. The resulting mixture was washed with diethyl ether (1×50 mL). The solids were collected by filtration to yield 3-ethyl-1-phenyl-1H-indazol-6-amine hydrochloride as a white solid.
Aufarbeitung
- customInto a 100-mL round-bottom flask, was placed
- concentrationThe resulting mixture was concentrated under vacuum
- washThe resulting mixture was washed with diethyl ether (1×50 mL)
- filtrationThe solids were collected by filtration
Quellen und Nachweise
- ORD-Eintrag
- ord-a5b2251b160c4d5dbe2f6231a3d00f66
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08822447B2
Verknüpfte Notizen
Wird geladen…