Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839327Generated: October 26, 2026

Chlorotrimethylsilane → HCID 23448979, compound

https://huagongshe.com/reaction/1839327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantAmmonium ChlorideHCID 25517—
Reactant7-Methylthioimidazo[5,1-b]thiazoleHCID 22631529—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23448979HCID 23448979—

Reaction Conditions

Temperature-30 °C

Reaction Steps

A 1.59 N n-butyllithium/n-hexane solution (9.91 ml) was added dropwise in an argon atmosphere at −50° C. to a solution of 2.55 g of 7-methylthioimidazo[5,1-b]thiazole in 100 ml of THF. The mixture was stirred at the same temperature for 25 min. Trimethylsilyl chloride (2.08 ml) was added thereto, and the mixture was stirred for 30 min. The temperature of the system was raised to −30° C. A 1.59 N n-butyllithium/n-hexane solution (5.72 ml) was added dropwise thereto, and the mixture was stirred at the same temperature for 30 min. An aqueous ammonium chloride solution was added to the reaction solution. The mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and then filtered. The solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:2) to give 2.58 g of 7-methylthio-2-trimethylsilylimidazo[5,1-b]-thiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677331B2
Source datasetuspto-grants-2004_01
ORD IDord-5c5c9b0f892d487d9c45612be8133314
Source noteuspto-grants-2004_01