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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839288Generated: October 26, 2026

S-Methyl methanethiosulfonate → 7-Methylthioimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1839288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantS-Methyl methanethiosulfonateHCID 18064—
ReactantAmmonium ChlorideHCID 25517—
Reactant7-Iodoimidazo[5,1-B]thiazoleHCID 17773777—
ReactantHCID 178420660HCID 178420660—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product7-Methylthioimidazo[5,1-b]thiazoleHCID 22631529—

Reaction Steps

A 1 M ethylmagnesium bromide/THF solution (1.4 ml) was added under ice cooling to a solution of 0.31 g of 7-iodoimidazo[5,1-b]thiazole in 3 ml of dry THF in an argon atmosphere. The mixture was stirred at the same temperature for one hr. Methyl methanethiolsulfonate (0.15 ml) was added thereto. The mixture was stirred at room temperature for 12 hr. A saturated aqueous ammonium chloride solution was added to the reaction solution. Ethyl acetate was added thereto. The mixture was washed with a dilute aqueous sodium thiosulfate solution 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 (ethyl acetate) to give 0.15 g of 7-methylthioimidazo[5,1-b]thiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677331B2
Source datasetuspto-grants-2004_01
ORD IDord-4d8ebec5080a4e22a5ea6c23983a8d8d
Source noteuspto-grants-2004_01