Reaktionsgleichung
[CH3:1][N:2]([CH3:5])[CH:3]=O.[Cl:6]C([O:9][C:10]([Cl:13])(Cl)Cl)=O.[NH2:14][C:15]1[S:16][CH:17]=[C:18](/[C:20](=[N:24]/[O:25][CH3:26])/C(O)=O)[N:19]=1.C(OC(C)C)(=O)C>O1CCCC1>[ClH:6].[CH3:1][N:2]([CH:3]=[N:14][C:15]1[S:16][CH:17]=[C:18](/[C:20](=[N:24]/[O:25][CH3:26])/[C:10]([Cl:13])=[O:9])[N:19]=1)[CH3:5]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Dimethylformamide (0.8 g, 11 mmol) was added to 9 ml of tetrahydrofuran, followed by ice-cooling. To the resulting mixture, 0.6 ml of trichloromethyl chloroformate was added dropwise under ice-cooling. After stirring the resulting mixture for 30 minutes, the mixture was cooled to -10° C. (Z)-2-(2-Amino-thiazol-4-yl)-2-methoxyiminoacetic acid (840 mg, 4.2 mmol) was added and the mixture so obtained was stirred for 2 hours. The mixture was added with 9 ml of isopropyl acetate, followed by stirring for 30 minutes. A precipitate was collected by filtration under a nitrogen gas stream and then dried at room temperature, whereby 1.23 g of the title compound were obtained (yield: 94%).
Aufarbeitung
- temperaturecooling
- temperaturecooling
- additionwas added
- customthe mixture so obtained
- stirringwas stirred for 2 hours
- stirringby stirring for 30 minutes
- filtrationA precipitate was collected by filtration under a nitrogen gas stream
- customdried at room temperature
Quellen und Nachweise
- ORD-Eintrag
- ord-a0f791409a584fea8fb7fb0116e3a933
- Quelldatensatz
- uspto-grants-1997_07
- Patentnummer
- US05650518
Verknüpfte Notizen
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