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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444162Generated: October 26, 2026

Potassium Hydroxide → 2-Bromoimidazo(4,3-b)(1,3)thiazole-7-carboxylic acid

https://huagongshe.com/reaction/1444162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl 2-bromoimidazo[5,1-b]thiazole-7-carboxylateHCID 59168405—
SolventMethanolHCID 887—
Product2-Bromoimidazo(4,3-b)(1,3)thiazole-7-carboxylic acidHCID 5916840499.5%

Reaction Steps

A 2 M aqueous solution (10 ml) of potassium hydroxide was added to a solution of ethyl 2-bromoimidazo[5,1-b]thiazole-7-carboxylate (265 mg, 0.96 mmol) in methanol (20 ml), and the mixture was stirred at room temperature for 18 hr. Methanol was removed by distillation under the reduced pressure, and the reaction solution was poured into 2 M hydrochloric acid (30 ml) under ice cooling to precipitate a solid. The resultant solid was washed with water, and a mixed solvent composed mainly of ethanol and toluene was added thereto. The solvent was removed by distillation under the reduced pressure, and the residue was thoroughly dried to give 2-bromoimidazo[5,1-b]thiazole-7-carboxylic acid (236 mg, quantitative) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662841B2
Source datasetuspto-grants-2010_02
ORD IDord-7bd160cc617245899a1454fe59ccf50e
Source noteuspto-grants-2010_02