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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444186Generated: November 1, 2026

Potassium sodium tartarate → 2-Bromo-7-hydroxymethylimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1444186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium sodium tartarateHCID 9855836—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantEthyl 2-bromoimidazo[5,1-b]thiazole-7-carboxylateHCID 59168405—
SolventTolueneHCID 1140—
Product2-Bromo-7-hydroxymethylimidazo[5,1-b]thiazoleHCID 5916840699.4%

Reaction Steps

A solution of ethyl 2-bromoimidazo[5,1-b] thiazole-7-carboxylate (52 mg, 0.19 mmol) in toluene (7 ml) was cooled to −78° C. A toluene solution of diisobutylaluminium hydride (1.01 M solution; 0.65 ml, 0.64 mmol) was added dropwise to the cooled solution, and the mixture was stirred at the same temperature for 40 min. After the completion of the reaction, a saturated aqueous potassium sodium tartrate solution was added thereto, and the mixture was stirred at room temperature for one hr and was extracted with ethyl acetate (5 ml×3). The organic layer was washed with saturated brine and was dried over anhydrous sodium sulfate, and the solvent was removed by distillation under the reduced pressure to give 2-bromo-7-hydroxymethylimidazo[5,1-b]thiazole (44 mg, 99%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662841B2
Source datasetuspto-grants-2010_02
ORD IDord-1cd86bb2bb4942b59a6979a2ed60012d
Source noteuspto-grants-2010_02