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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444174Generated: November 1, 2026

Benzoic Acid → 2-Bromoimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1444174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
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 1046546849.2%

Reaction Conditions

Temperature180 °C

Reaction Steps

A solution of 2-bromoimidazo[5,1-b]thiazole-7-carboxylic acid (32 mg, 0.13 mmol) and benzoic acid (16 mg, 0.13 mmol) dissolved 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 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 then removed by distillation under the reduced pressure, and the residue was thoroughly dried to give 2-bromoimidazo[5,1-b]thiazole (13 mg, 49%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662841B2
Source datasetuspto-grants-2010_02
ORD IDord-3bd36ce111ca4cee80cc8b9652fb51b8
Source noteuspto-grants-2010_02