HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-Bromoimidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Bromoimidazo(4,3-b)(1,3)thiazole-7-carboxylic acid | HCID 59168404 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | 2-Bromoimidazo[5,1-b]thiazole | HCID 10465468 | 49.2% |
Reaction Steps
A solution of 2-bromoimidazo[5,1-b]thiazole-7-carboxylic acid (28 mg, 0.11 mmol) in ethylene glycol (1 ml) was stirred at 180° C. for 2.5 hr. The reaction solution was allowed to cool to room temperature, a 2.7 M aqueous solution (5 ml) of sodium hydroxide was added to the cooled solution, and the mixture was extracted with ethyl acetate (5 ml×3). The organic layer was washed with saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure to give 2-bromoimidazo[5,1-b]thiazole (11 mg, 48%) as a crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07662841B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-2569992b85f94ea9b6c56f9274a54719 |
| Source note | uspto-grants-2010_02 |