HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic Acid → 2-Bromoimidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | 2-Bromoimidazo(4,3-b)(1,3)thiazole-7-carboxylic acid | HCID 59168404 | — |
| Solvent | 1,2,4-Trichlorobenzene | HCID 13 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-Bromoimidazo[5,1-b]thiazole | HCID 10465468 | 49.2% |
Reaction Conditions
| Temperature | 180 °C |
|---|
Reaction Steps
A solution of 2-bromoimidazo[5,1-b]thiazole-7-carboxylic acid (32 mg, 0.13 mmol) and benzoic acid (16 mg, 0.13 mmol) dissolved in 1,2,4-trichlorobenzene (1 ml) was stirred at 180° C. for 24 hr. The reaction solution was allowed to cool to room temperature, was diluted with hexane, and was extracted with 2 M hydrochloric acid (3 ml×3). The aqueous layer was neutralized with a 2 M aqueous solution of sodium hydroxide and 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 then removed by distillation under the reduced pressure, and the residue was thoroughly dried to give 2-bromoimidazo[5,1-b]thiazole (13 mg, 49%) 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-3bd36ce111ca4cee80cc8b9652fb51b8 |
| Source note | uspto-grants-2010_02 |