HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230034Generated: October 25, 2026
Ammonium Chloride → 2-Bromo-7-(pyridin-3-yl)hydroxymethylimidazo[5,1-b]thiazole
https://huagongshe.com/reaction/230034
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Iodopyridine | HCID 70714 | — |
| Reactant | 2-Bromoimidazo[5,1-b]thiazole-7-carbaldehyde | HCID 11528744 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-7-(pyridin-3-yl)hydroxymethylimidazo[5,1-b]thiazole | HCID 23088795 | — |
Reaction Steps
A 1 M tetrahydrofuran solution (0.9 ml) of ethylmagnesium bromide was added to a solution of 147 mg of 3-iodopyridine in 1 ml of tetrahydrofuran under an argon atmosphere, and the mixture was stirred at room temperature for 30 min. A solution of 149 mg of 2-bromo-7-formylimidazo[5,1-b]thiazole in 2 ml of tetrahydrofuran was added to the solution, and the mixture was stirred at that temperature for 2.5 hr. An aqueous saturated ammonium chloride solution was added to the reaction mixture to stop the reaction, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine in that order and was then dried over magnesium sulfate. The solvent was removed by evaporation, and the residue was purified by column chromatography on silica gel (ethyl acetate:methanol=4:1) to give 147 mg of 2-bromo-7-(pyridin-3-yl)hydroxymethylimidazo[5,1-b]thiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07563901B2 |
|---|
| Source dataset | uspto-grants-2009_07 |
|---|
| ORD ID | ord-255fcc0aefa748c88a0f4baca515730b |
|---|
| Source note | uspto-grants-2009_07 |
|---|