Ethanol → 3-Methyl[1,3]thiazolo[3,2-a]benzimidazole
Reaktionsgleichung
[SH:1][C:2]1[NH:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.[CH3:11][CH2:12]O.[OH-].[K+].[CH3:16]COC(C)=O>>[CH3:16][C:12]1[N:6]2[C:2](=[N:3][C:4]3[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=32)[S:1][CH:11]=1Komponenten
Versuchsvorschrift
2-Mercaptobenzoimidazole (15.0 g) was added to EtOH (100 ml) solution of KOH (6.60 g), and the mixture was heated under reflux for 1 hour. After cooling to room temperature, this was mixed with 2-chloroacetone (7.96 ml) and stirred overnight. The reaction solution was mixed with EtOAc and stirred, the insoluble matter was removed by filtration and then the solvent was evaporated under a reduced pressure. The thus obtained oily material was dissolved in concentrated sulfuric acid (100 ml) and stirred at room temperature for 6 hours. The reaction solution was poured into ice water and then neutralized with 28% NH3 aqueous solution, and the resulting precipitate was collected by filtration. This was recrystallized from MeOH to obtain the title compound (9.60 g) as light brown crystals. (J. O. C., 29 (4), 865-9 (1964))
Aufarbeitung
- temperaturethe mixture was heated
- temperatureunder reflux for 1 hour
- stirringstirred
- customthe insoluble matter was removed by filtration
- customthe solvent was evaporated under a reduced pressure
- dissolutionThe thus obtained oily material was dissolved in concentrated sulfuric acid (100 ml)
- stirringstirred at room temperature for 6 hours
- additionThe reaction solution was poured into ice water
- filtrationthe resulting precipitate was collected by filtration
- customThis was recrystallized from MeOH
Quellen und Nachweise
- ORD-Eintrag
- ord-e71f72a8e04b47a687b2f30222c34596
- Quelldatensatz
- uspto-grants-2003_11
- Patentnummer
- US06642264B1
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