Acetyl chloride → 5-Acetyl-7-methylthioimidazo[5,1-b]thiazole
Reaktionsgleichung
C([Mg]Br)C.C1C[O:8][CH2:7][CH2:6]1.I[C:11]1[N:18]2[C:14]([S:15][CH:16]=[CH:17]2)=[C:13]([S:19][CH3:20])[N:12]=1.C(Cl)(=O)C.[Cl-].[NH4+]>C1COCC1.C(OCC)(=O)C>[C:7]([C:11]1[N:18]2[C:14]([S:15][CH:16]=[CH:17]2)=[C:13]([S:19][CH3:20])[N:12]=1)(=[O:8])[CH3:6]Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- -5 °C
Versuchsvorschrift
A 1 M ethylmagnesium bromide/THF solution (4.78 ml) was added in an argon atmosphere at −40° C. to a solution of 963 mg of 5-iodo-7-methylthioimidazo[5,1-b]thiazole in 30 ml of dry THF. The mixture was stirred at the same temperature for 30 min. Acetyl chloride (0.35 ml) was added thereto. The temperature of the system was raised to −5° C. over a period of 2 hr. A saturated aqueous ammonium chloride solution was added to the reaction mixture. Ethyl acetate was added thereto, followed by washing with a dilute aqueous sodium thiosulfate solution and saturated brine in that order. The organic layer was dried over anhydrous magnesium sulfate. The solvent was removed by distillation. The residue was purified by column chromatography on silica gel (dichloromethane:ethyl acetate:hexane=2:1:1) to give 384 mg of 5-acetyl-7-methylthioimidazo[5,1-b]thiazole.
Aufarbeitung
- washby washing with a dilute aqueous sodium thiosulfate solution and saturated brine in that order
- dry with materialThe organic layer was dried over anhydrous magnesium sulfate
- customThe solvent was removed by distillation
- customThe residue was purified by column chromatography on silica gel (dichloromethane:ethyl acetate:hexane=2:1:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-d411427771104247aeae62642b245c5e
- Quelldatensatz
- uspto-grants-2004_01
- Patentnummer
- US06677331B2
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