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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-7-hydroxymethylimidazo[5,1-b]thiazole | HCID 59168406 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Product | 2-Bromoimidazo[5,1-b]thiazole-7-carbaldehyde | HCID 11528744 | 18.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07662841B2 |
|---|
| Source dataset | uspto-grants-2010_02 |
|---|
| ORD ID | ord-acde176a0c6948dbae051a54570d33e1 |
|---|
| Source note | uspto-grants-2010_02 |
|---|