5-Acetyl-2-amino-4-methylthiazole → HCID 20145033, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1[S:3][C:4]([C:8](=[O:10])[CH3:9])=[C:5]([CH3:7])[N:6]=1.[BrH:11].[NH+]1C=CC=CC=1>Br.C(O)(=O)C>[BrH:11].[NH2:1][C:2]1[S:3][C:4]([C:8](=[O:10])[CH2:9][Br:11])=[C:5]([CH3:7])[N:6]=1Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
To a suspension of 2-amino-4-methyl-5-acetylthiazole (15.6 g) in 30% of hydrogen bromide in acetic acid (120 ml) was added pyridinium hydrobromide perbromide (36 g) at ambient temperature and the mixture was stirred at the same temperature for 5 hours. The precipitate was collected by filtration, washed with diisopropyl ether, and dried over calcium chloride to give 2-amino-4-methyl-5-(2-bromoacetyl)thiazole hydrobromide (26.8 g).
Aufarbeitung
- filtrationThe precipitate was collected by filtration
- washwashed with diisopropyl ether
- dry with materialdried over calcium chloride
Quellen und Nachweise
- ORD-Eintrag
- ord-164acf50a3584ea98dae9908e2abc658
- Quelldatensatz
- uspto-grants-1988_04
- Patentnummer
- US04735957
Notizen zur Reaktion
Wird geladen…