Reaktionsgleichung
[ClH:1].C(=[N:15][NH:16][C:17]1[CH:26]=[C:25]([F:27])[C:20]2[NH:21][C:22]([CH3:24])=[N:23][C:19]=2[CH:18]=1)(C1C=CC=CC=1)C1C=CC=CC=1>C(O)C>[ClH:1].[ClH:1].[F:27][C:25]1[C:20]2[NH:21][C:22]([CH3:24])=[N:23][C:19]=2[CH:18]=[C:17]([NH:16][NH2:15])[CH:26]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 61.5 °C
Versuchsvorschrift
Concentrated hydrochloric acid (0.7 ml) was added to a mixture of the crude N-benzhydrylidene-N′-(7-fluoro-2-methyl-1H-benzimidazol-5-yl)-hydrazine (325 mg) and ethanol (0.7 ml). This was stirred at 59 to 64° C. for one hour, and the reaction mixture was cooled to room temperature. Then, the precipitated solid was collected by filtration and dried. Thus, 7-fluoro-2-methyl-1H-benzimidazol-5-yl-hydrazine dihydrochloride (90 mg, 80%) was obtained.
Aufarbeitung
- temperaturethe reaction mixture was cooled to room temperature
- filtrationThen, the precipitated solid was collected by filtration
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-3e6298c77679466680a8fed572bdbf52
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08829199B2
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