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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839308Generated: November 1, 2026

Phosphate → Methyl 2-(tri-n-butylstannyl)imidazo[5,1-b]thiazole-7-carboxylate

https://huagongshe.com/reaction/1839308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantTributyltin ChlorideHCID 15096—
ReactantMethyl imidazo[5,1-b]thiazole-7-carboxylateHCID 23448997—
ReactantLithium bis(trimethylsilyl)amide hexaneHCID 86588928—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(tri-n-butylstannyl)imidazo[5,1-b]thiazole-7-carboxylateHCID 23449182—

Reaction Conditions

Temperature-50 °C

Reaction Steps

A solution (5 ml) of 0.716 g of tri-n-butylstannyl Chloride in THF was added to a solution (20 ml) of 0.364 g of methyl imidazo[5,1-b]thiazole-7-carboxylate in THF at −70° C. A 1.0 N lithiumbis(trimethylsilyl)amide/n-hexane solution (4.4 ml) was added dropwise thereto at −70° C. The mixture was stirred at −50° C. for 30 min. The reaction solution was added to an ice cold mixed solution composed of 50 ml of 0.2 N phosphate buffer (ph 7) and 50 ml of dichloromethane with stirring. The organic layer was separated, and then dried over anhydrous magnesium sulfate. The solvent was removed by distillation. The residue was subjected to separation and purification by flash column chromatography on silica gel (hexane:ethyl acetate=1:1) to give 0.395 g of the title, compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677331B2
Source datasetuspto-grants-2004_01
ORD IDord-5baaa9b65e3c4322bf777745abb5ef58
Source noteuspto-grants-2004_01