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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444173Generated: November 1, 2026

Phenol → 2-Bromoimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1444173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
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 1046546853.4%

Reaction Conditions

Temperature180 °C

Reaction Steps

A solution of 2-bromoimidazo[5,1-b]thiazole-7-carboxylic acid (31 mg, 0.12 mmol) and phenol (12 mg, 0.12 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 1 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. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:1) to give 2-bromoimidazo[5,1-b]thiazole (13 mg, 50%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662841B2
Source datasetuspto-grants-2010_02
ORD IDord-d5b96680bd9b4229956cf053eaad78d1
Source noteuspto-grants-2010_02