Chlorotrimethylsilane → HCID 23449325, compound
Reaction equation
C([Li])CCC.CCCCCC.[S:12]1[CH:16]=[CH:15][N:14]2[CH:17]=[N:18][CH:19]=[C:13]12.[CH3:20][Si:21](Cl)([CH3:23])[CH3:22].[Cl-].[NH4+]>C1COCC1.C(OCC)(=O)C>[CH3:20][Si:21]([CH3:23])([CH3:22])[C:16]1[S:12][C:13]2=[CH:19][N:18]=[CH:17][N:14]2[CH:15]=1Participants
Procedure
A 1.6 N n-butyllithium/n-hexane, solution (16.7 ml) was added in an argon atmosphere at −50° C. to a solution of 3.17 g of imidazo[5,1-b]thiazole in 120 ml of dry THF. The mixture was stirred at the same temperature for 30 min. Trimethylsilyl chloride (3.54 ml) was added thereto, and the mixture was stirred for 20 min. A 1.6 N n-butyllithium/n-hexane solution (8.0 ml) was added thereto, and the mixture was stirred for 20 min. A saturated aqueous ammonium chloride solution was added to the reaction mixture. Ethyl acetate was then added thereto, followed by washing with water 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 (ethyl acetate) to give 4.53 g of 2-(trimethylsilyl)imidazo[5,1-b]thiazole.
Workup
- stirringthe mixture was stirred for 20 min
- stirringthe mixture was stirred for 20 min
- washby washing with water 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 (ethyl acetate)
Sources & evidence
- ORD record
- ord-a771298499ac4b32a03151e76506506d
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06677331B2
Reaction notes
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