Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444176Generated: November 1, 2026

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

https://huagongshe.com/reaction/1444176

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 1046546818.9%

Reaction Steps

A solution of 2-bromoimidazo[5,1-b]thiazole-7-carboxylic acid (33 mg, 0.13 mmol) in 1,2,4-trichlorobenzene (1 ml) was stirred at 180° C. for 24 hr. The reaction solution was allowed to cool to room temperature, was diluted with hexane, and was extracted with 2 M hydrochloric acid (3 ml×3). The aqueous layer was neutralized with a 2 M aqueous solution of sodium hydroxide and was then extracted with ethyl acetate (5 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 thoroughly dried to give 2-bromoimidazo[5,1-b]thiazole (5 mg, 15%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662841B2
Source datasetuspto-grants-2010_02
ORD IDord-a64f5c9604fe4f4d9b6eaf4880ab30ed
Source noteuspto-grants-2010_02