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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989864Generated: October 29, 2026

Chlorotrimethylsilane → HCID 23449325, compound

https://huagongshe.com/reaction/989864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantAmmonium ChlorideHCID 25517—
ReactantImidazo[5,1-b]thiazoleHCID 21262404—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 23449325HCID 23449325—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458780B1
Source datasetuspto-grants-2002_10
ORD IDord-9c65c9a92d51473486a0f0d57c10b1fd
Source noteuspto-grants-2002_10