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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444190Generated: November 2, 2026

2-Bromo-7-hydroxymethylimidazo[5,1-b]thiazole → 2-Bromoimidazo[5,1-b]thiazole-7-carbaldehyde

https://huagongshe.com/reaction/1444190

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-7-hydroxymethylimidazo[5,1-b]thiazoleHCID 59168406—
ReactantHCID 178418287HCID 178418287—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventSulfuric acid magnesium salt (1:1)HCID 24083—
Product2-Bromoimidazo[5,1-b]thiazole-7-carbaldehydeHCID 1152874418.2%

Reaction Steps

A solution of 2-bromo-7-hydroxymethylimidazo [5,1-b]thiazole (44 mg, 0.19 mmol) in dichloromethane (4 ml) was added to a suspension of pyridinium chlorochromate (121 mg, 0.56 mmol) in dichloromethane (2 ml), and the mixture was stirred at room temperature for 30 min. After the completion of the reaction, the reaction solution was diluted with diethyl ether, anhydrous magnesium sulfate was added thereto, and the mixture was stirred at room temperature for additional 10 min. The reaction mixture was filtered through Celite. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography on silica gel (ethyl acetate:methanol=60:1) to give 2-bromoimidazo[5,1-b]thiazole-7-carbaldehyde (8 mg, 18%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662841B2
Source datasetuspto-grants-2010_02
ORD IDord-acde176a0c6948dbae051a54570d33e1
Source noteuspto-grants-2010_02