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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444168Generated: November 2, 2026

Acetic Anhydride → 2-Bromoimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1444168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
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 1046546867.3%

Reaction Conditions

Temperature150 °C

Reaction Steps

Acetic anhydride (0.1 ml, 1.06 mmol) was added to a solution of 2-bromoimidazo[5,1-b]thiazole-7-carboxylic acid (38 mg, 0.15 mmol) in 1,2,4-trichlorobenzene (1 ml), and the mixture was stirred at 150° C. for 2 hr. The reaction solution was allowed to cool to room temperature, was diluted with hexane, and was extracted with 1 M hydrochloric acid (2 ml×3). The aqueous layer was neutralized with a 2 M aqueous solution of sodium hydroxide and was then extracted with ethyl acetate (4 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 purified by column chromatography on silica gel (hexane:ethyl acetate=1:1→1:2) to give 2-bromoimidazo[5,1-b]thiazole (20.5 mg, 66%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662841B2
Source datasetuspto-grants-2010_02
ORD IDord-6e47651ce1c44242ae3bd2505f3aa805
Source noteuspto-grants-2010_02