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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839318Generated: November 2, 2026

Sodium Chloride → 7-(Thiazol-4-yl)-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1839318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantTributyltin ChlorideHCID 15096—
Reactant7-(Thiazol-4-yl)imidazo[5,1-b]thiazoleHCID 23449111—
ReactantLiHMDS tetrahydrofuranHCID 23714775—
SolventTetrahydrofuranHCID 8028—
Product7-(Thiazol-4-yl)-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazoleHCID 23449257—

Reaction Conditions

Temperature-30 °C

Reaction Steps

A solution of 1.01 g of 7-(thiazol-4-yl)imidazo[5,1-b]thiazole in 45 ml of THF was cooled to −70° C. in an argon atmosphere. Tri-n-butylstannyl chloride (1.58 ml) was added thereto. A 1 N lithiumbis(trimethylsilyl)amide/THF solution (11.2 ml) was added dropwise at the same temperature. The mixture was stirred for 30 min. The temperature of the mixture was raised to −30° C. over a period of one hr. A saturated aqueous sodium chloride solution was added thereto, followed by extraction twice with ethyl acetate. The extract was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:1). The title compound (294 mg) was obtained from the fraction of Rf=0.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677331B2
Source datasetuspto-grants-2004_01
ORD IDord-1e73019ad5174d1ca2e85582ca4418d0
Source noteuspto-grants-2004_01