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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839313Generated: October 30, 2026

Triethylamine → 7-(t-Butyldimethylsilylsulfamoyl)imidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1839313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant7-Sulfamoylimidazo[5,1-b]thiazoleHCID 23449139—
SolventDimethylformamideHCID 6228—
Product7-(t-Butyldimethylsilylsulfamoyl)imidazo[5,1-b]thiazoleHCID 17811066—

Reaction Steps

t-Butyldimethylsilyl chloride (0.30 g) and 0.33 ml of triethylamine were added to a solution of 0.20 g of 7-sulfamoylimidazo[5,1-b]thiazole in 5 ml of DMF. The mixture was stirred at room temperature for one hr. Ethyl acetate was added to the reaction mixture, 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 (hexane:ethyl acetate=1:1) to give 0.34 of 7-(t-butyldimethylsilylsulfamoyl)imidazo[5,1-b]thiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677331B2
Source datasetuspto-grants-2004_01
ORD IDord-b8f13980e84544b0ba42ca0e5a31f8b8
Source noteuspto-grants-2004_01