Sodium Chloride → 7-(Thiazol-4-yl)-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazole
Reaktionsgleichung
[S:1]1[CH:5]=[C:4]([C:6]2[N:7]=[CH:8][N:9]3[CH:13]=[CH:12][S:11][C:10]=23)[N:3]=[CH:2]1.[CH2:14]([Sn:18](Cl)([CH2:23][CH2:24][CH2:25][CH3:26])[CH2:19][CH2:20][CH2:21][CH3:22])[CH2:15][CH2:16][CH3:17].C[Si]([N-][Si](C)(C)C)(C)C.[Li+].C1COCC1.[Cl-].[Na+]>C1COCC1>[S:1]1[CH:5]=[C:4]([C:6]2[N:7]=[CH:8][N:9]3[CH:13]=[C:12]([Sn:18]([CH2:19][CH2:20][CH2:21][CH3:22])([CH2:23][CH2:24][CH2:25][CH3:26])[CH2:14][CH2:15][CH2:16][CH3:17])[S:11][C:10]=23)[N:3]=[CH:2]1Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- -30 °C
Versuchsvorschrift
A solution of 1.01 g of 7-(thiazol-4-yl)imidazo[5,1-b]thiazole in 45 ml of THF was cooled to −70° C. in an argon atmosphere. Tri-n-butylstannyl chloride (1.58 ml) was added thereto. A 1 N lithiumbis(trimethylsilyl)amide/THF solution (11.2 ml) was added dropwise at the same temperature. The mixture was stirred for 30 min. The temperature of the mixture was raised to −30° C. over a period of one hr. A saturated aqueous sodium chloride solution was added thereto, followed by extraction twice with ethyl acetate. The extract was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:1). The title compound (294 mg) was obtained from the fraction of Rf=0.5.
Aufarbeitung
- extractionfollowed by extraction twice with ethyl acetate
- dry with materialThe extract was dried over anhydrous magnesium sulfate
- customThe solvent was removed by distillation under the reduced pressure
- customThe residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-1e73019ad5174d1ca2e85582ca4418d0
- Quelldatensatz
- uspto-grants-2004_01
- Patentnummer
- US06677331B2
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