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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113289Generated: October 30, 2026

Ammonium Chloride → 2-Bromo-7-(pyridin-3-yl)hydroxymethylimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/2113289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant3-IodopyridineHCID 70714—
Reactant2-Bromoimidazo[5,1-b]thiazole-7-carbaldehydeHCID 11528744—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-7-(pyridin-3-yl)hydroxymethylimidazo[5,1-b]thiazoleHCID 23088795—

Reaction Steps

A 1 M tetrahydrofuran solution (0.9 ml) of ethylmagnesium bromide was added to a solution of 147 mg of 3-iodopyridine in 1 ml of tetrahydrofuran under an argon atmosphere, and the mixture was stirred at room temperature for 30 min. A solution of 149 mg of 2-bromo-7-formylimidazo[5,1-b]thiazole in 2 ml of tetrahydrofuran was added to the solution, and the mixture was stirred at that temperature for 2.5 hr. An aqueous saturated ammonium chloride solution was added to the reaction mixture to stop the reaction, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine in that order and was then dried over magnesium sulfate. The solvent was removed by evaporation, and the residue was purified by column chromatography on silica gel (ethyl acetate:methanol=4:1) to give 147 mg of 2-bromo-7-(pyridin-3-yl)hydroxymethylimidazo[5,1-b]thiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524951B2
Source datasetuspto-grants-2009_04
ORD IDord-f34cedd1f50c4fb0b3f5c52fbac03677
Source noteuspto-grants-2009_04