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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Ethyl 2-bromoimidazo[5,1-b]thiazole-7-carboxylate | HCID 59168405 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Bromo-7-hydroxymethylimidazo[5,1-b]thiazole | HCID 59168406 | 99.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662841B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-1cd86bb2bb4942b59a6979a2ed60012d |
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| Source note | uspto-grants-2010_02 |
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