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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839315Generated: November 2, 2026

Water → 7-(2-Methoxycarbonylvinyl)-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1839315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTributyltin ChlorideHCID 15096—
ReactantLiHMDS tetrahydrofuranHCID 23714775—
Reactant7-(2-Methoxycarbonylvinyl)imidazo[5,1-b]thiazoleHCID 69930338—
SolventTetrahydrofuranHCID 8028—
Product7-(2-Methoxycarbonylvinyl)-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazoleHCID 69927972—

Reaction Steps

Tri-n-butylstannyl chloride (250 μl) and 2.1 ml of a 1.0 N lithiumbis(trimethylsilyl)amide/THF solution were added in that order to a solution of 7-(2-methoxycarbonylvinyl)imidazo[5,1-b]thiazole (a mixture of geometrical isomers) in dry THF in an argon atmosphere at −78° C. The mixture was stirred at the same temperature for 15 min. Water was added thereto. The mixture was extracted with ethyl acetate, followed by washing with saturated brine. 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=4:1) to give 408 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677331B2
Source datasetuspto-grants-2004_01
ORD IDord-59b08b8dec214cc8b9e9c08f503ae8bb
Source noteuspto-grants-2004_01