HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoimidazo(4,3-b)(1,3)thiazole-7-carboxylic acid → 2-Bromoimidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoimidazo(4,3-b)(1,3)thiazole-7-carboxylic acid | HCID 59168404 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Bromoimidazo[5,1-b]thiazole | HCID 10465468 | 21.9% |
Reaction Steps
A solution of 2-bromoimidazo[5,1-b]thiazole-7-carboxylic acid (22 mg, 0.09 mmol) in dimethyl sulfoxide (1 ml) was stirred at 180° C. for 2 hr. Thereafter, the reaction solution was allowed to cool to room temperature and was then concentrated by removal of the solvent under the reduced pressure. The residue was purified by column chromatography on silica gel (ethyl acetate:methanol=60:1) to give 2-bromoimidazo[5,1-b]thiazole (4 mg, 20%) 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-224c4d9bcf364333a2efc117422f5526 |
| Source note | uspto-grants-2010_02 |