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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989848Generated: October 30, 2026

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

https://huagongshe.com/reaction/989848

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 17811066108.8%

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 5ml 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 g of 7-(t-butyldimethylsilylsulfamoyl)imidazo[5,1-b]thiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458780B1
Source datasetuspto-grants-2002_10
ORD IDord-e9ccdbaa84dd4a24908599001879875e
Source noteuspto-grants-2002_10