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 | Acetic Acid | HCID 176 | — |
| Product | 2-Bromoimidazo[5,1-b]thiazole | HCID 10465468 | 14.1% |
Reaction Steps
A solution of 2-bromoimidazo[5,1-b]thiazole-7-carboxylic acid (36 mg, 0.14 mmol) in acetic acid (1 ml) was heated under reflux for 2 days. The reaction solution was allowed to cool to room temperature and was then concentrated by removal of the solvent under the reduced pressure, and the residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:1) to give 2-bromoimidazo[5,1-b]thiazole (4 mg, 14%) 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-f0fbcf03566c4738b21a9aa60504c52e |
| Source note | uspto-grants-2010_02 |