Hydrochloric Acid → HCID 18785143, Verbindung
Reaktionsgleichung
C(OC([N:8]1[C:12]2[C:13]([F:19])=[CH:14][C:15]([NH2:18])=[C:16]([CH3:17])[C:11]=2[N:10]=[CH:9]1)=O)(C)(C)C.[ClH:20]>>[ClH:20].[CH3:17][C:16]1[C:11]2[NH:10][CH:9]=[N:8][C:12]=2[C:13]([F:19])=[CH:14][C:15]=1[NH2:18]Komponenten
3
Versuchsvorschrift
1-tert-Butoxycarbonyl-4-methyl-5-amino-7-fluorobenzimidazole (1 g) (prepared as described in U.S. Pat. No. 5,478,858 issued to Cupps and Bogdan, Dec. 26, 1995, incorporated herein by reference) and 6N HCl (10 mL) are combined and heated to reflux while stirring. After completion of the t-BOC group deprotection, the reaction mixture is concentrated under reduced pressure and dried to furnish 4methyl-5-amino-7-fluorobenzimidazole hydrochloride.
Aufarbeitung
- temperatureheated
- temperatureto reflux
- concentrationAfter completion of the t-BOC group deprotection, the reaction mixture is concentrated under reduced pressure
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-25207606004a45c7b45f8040b0f4e281
- Quelldatensatz
- uspto-grants-2000_05
- Patentnummer
- US06066740
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