Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444165Generated: November 1, 2026

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

https://huagongshe.com/reaction/1444165

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 1046546880.6%

Reaction Steps

A solution of 2-bromoimidazo[5,1-b]thiazole-7-carboxylic acid (27 mg, 0.11 mmol) in 1,2,4-trichlorobenzene (1 ml) was stirred at 210° C. for one hr and then at 220° C. for 30 min. The reaction solution was allowed to cool to room temperature and was diluted with hexane, followed by extraction with 2 M hydrochloric acid (3 ml×3). The aqueous layer was neutralized with a 2 M aqueous solution of sodium hydroxide and was 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 (18 mg, 80%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662841B2
Source datasetuspto-grants-2010_02
ORD IDord-78e576679e464b0e8ba7cadbe59725a8
Source noteuspto-grants-2010_02