Hydrochloric Acid → HCID 10037407, Verbindung
Reaktionsgleichung
[CH3:1][C:2]1[NH:3][C:4](=[O:14])[CH2:5][S:6][C:7]=1[C:8]1[CH:13]=[CH:12][N:11]=[CH:10][CH:9]=1.[ClH:15]>CO>[ClH:15].[CH3:1][C:2]1[NH:3][C:4](=[O:14])[CH2:5][S:6][C:7]=1[C:8]1[CH:13]=[CH:12][N:11]=[CH:10][CH:9]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 5-methyl-6-(4-pyridinyl)-2H-1,4-thiazin-3(4H)-one (5 g) in methanol (500 ml), 12N hydrochloric acid (4 ml) was added dropwise with stirring at room temperature. The reaction mixture was stirred at room temperature for 1 hour and then concentrated in vacuo. Tetrahydrofuran (200 ml) was added and the reaction mixture was stirred at room temperature for 10 minutes, and then filtered. The residue was recrystallized from ethanol to give 4.6 g of 5-methyl-6-(4-pyridinyl)-2H-1,4-thiazin-3(4H)-one hydrochloride as pale yellow needles.
Aufarbeitung
- stirringThe reaction mixture was stirred at room temperature for 1 hour
- concentrationconcentrated in vacuo
- additionTetrahydrofuran (200 ml) was added
- stirringthe reaction mixture was stirred at room temperature for 10 minutes
- filtrationfiltered
- customThe residue was recrystallized from ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-c42afcba0ee649bfa06367f523f8df78
- Quelldatensatz
- uspto-grants-1986_01
- Patentnummer
- US04565813
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