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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444166Generated: October 30, 2026

2-Bromoimidazo(4,3-b)(1,3)thiazole-7-carboxylic acid → 2-Bromoimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1444166

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromoimidazo(4,3-b)(1,3)thiazole-7-carboxylic acidHCID 59168404—
Solvent1,2,4-TrichlorobenzeneHCID 13—
SolventHexaneHCID 8058—
Product2-Bromoimidazo[5,1-b]thiazoleHCID 1046546884%

Reaction Steps

A solution of 2-bromoimidazo[5,1-b]thiazole-7-carboxylic acid (1.08 g, 4.37 mmol) in 1,2,4-trichlorobenzene (20 ml) was stirred at 220° C. for 4 hr. The reaction solution was allowed to cool to room temperature, was diluted with hexane, and was extracted with 4 M hydrochloric acid (8 ml×3). The aqueous layer was neutralized with a 10 M aqueous solution of sodium hydroxide and was extracted with ethyl acetate (10 ml×3). The organic layer was washed with saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:1→1:2) to give 2-bromoimidazo[5,1-b]thiazole (744.8 mg, 84%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662841B2
Source datasetuspto-grants-2010_02
ORD IDord-c1678df5dfe0494bb5f4b4845cb4b9d3
Source noteuspto-grants-2010_02