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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989835Generated: October 25, 2026

Tributyltin Chloride → 7-(4-Nitrobenzylsulfamoyl)-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazole

https://huagongshe.com/reaction/989835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
ReactantAmmonium ChlorideHCID 25517—
Reactant7-(4-Nitrobenzylsulfamoyl)imidazo[5,1-b]thiazoleHCID 23449305—
ReactantLithium bis(trimethylsilyl)amide hexaneHCID 86588928—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventHexamethylphosphoramideHCID 12679—
Product7-(4-Nitrobenzylsulfamoyl)-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazoleHCID 23449191—

Reaction Steps

A 1.0 N lithiumbis(trimethylsilyl)amide/n-hexane solution (4.8 ml) was added to a solution of 0.68 g of 7-(4-nitrobenzylsulfamoyl)imidazo[5,1-b]thiazole in 20 ml of THF and 4 ml of HMPA in an argon atmosphere at −40° C. The mixture was stirred at the same temperature for 30 min. Tri-n-butylstannyl chloride (0.57 ml) was added thereto. The mixture was stirred at the same temperature for 30 min. A saturated aqueous ammonium chloride solution was added thereto. Ethyl acetate was then added thereto. The mixture was then washed 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 0.78 g of the tile compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458780B1
Source datasetuspto-grants-2002_10
ORD IDord-86b7465cf28a4d16b4d2f376e8710c63
Source noteuspto-grants-2002_10