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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444169Generated: November 1, 2026

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

https://huagongshe.com/reaction/1444169

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromoimidazo(4,3-b)(1,3)thiazole-7-carboxylic acidHCID 59168404—
SolventDimethyl SulfoxideHCID 679—
Product2-Bromoimidazo[5,1-b]thiazoleHCID 1046546821.9%

Reaction Steps

A solution of 2-bromoimidazo[5,1-b]thiazole-7-carboxylic acid (22 mg, 0.09 mmol) in dimethyl sulfoxide (1 ml) was stirred at 180° C. for 2 hr. Thereafter, the reaction solution was allowed to cool to room temperature and was then concentrated by removal of the solvent under the reduced pressure. The residue was purified by column chromatography on silica gel (ethyl acetate:methanol=60:1) to give 2-bromoimidazo[5,1-b]thiazole (4 mg, 20%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662841B2
Source datasetuspto-grants-2010_02
ORD IDord-224c4d9bcf364333a2efc117422f5526
Source noteuspto-grants-2010_02