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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989811Generated: October 31, 2026

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

https://huagongshe.com/reaction/989811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
ReactantAmmonium ChlorideHCID 25517—
Reactant7-Hydroxyiminomethylimidazo[5,1-b]thiazoleHCID 85769405—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
SolventHexamethylphosphoramideHCID 12679—
Product7Hydroxyiminomethyl-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazoleHCID 85769406—

Reaction Conditions

Temperature-40 °C

Reaction Steps

7-Hydroxyiminomethylimidazo[5,1-b]thiazole (a low-polarity geometrical isomer) (831 mg) was dissolved in 25 ml of THF and 5 ml of hexamethylphosphoramide (HMPA). A 1.55 N n-butyllithium/n-hexane solution (7.67 ml) was dropwise added in an argon atmosphere at −70° C. to the solution. The mixture was stirred at the same temperature for 40 min. Tri-n-butylstannyl chloride (1.84 ml) was added thereto. The mixture was stirred for 1.5 hr while raising the temperature to −40° C. An ammonium chloride solution was added to the reaction solution, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=3:1 to 1:1) to give 680 mg of 7hydroxyiminomethyl-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazole (a geometrical isomer derived from a starting compound as a low-polarity oxime isomer).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458780B1
Source datasetuspto-grants-2002_10
ORD IDord-1eeebb371f774c8296e0e0e96baec152
Source noteuspto-grants-2002_10