HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444167Generated: October 30, 2026
Acetic Anhydride → 2-Bromoimidazo[5,1-b]thiazole
https://huagongshe.com/reaction/1444167
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| 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 | 78.1% |
Reaction Steps
Acetic anhydride (0.1 ml, 1.06 mmol) was added to a solution of 2-bromoimidazo[5,1-b]thiazole-7-carboxylic acid (36 mg, 0.14 mmol) in 1,2,4-trichlorobenzene (1 ml), and the mixture was stirred at 130° C. for 24 hr. The reaction solution was allowed to cool to room temperature, was diluted with hexane, and was extracted with 1 M hydrochloric acid (2 ml×3). The aqueous layer was neutralized with a 2 M aqueous solution of sodium hydroxide and was extracted with ethyl acetate (4 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, and the residue was purified by column chromatography on silica gel (hexane:ethyl acetate =1:1→1:2) to give 2-bromoimidazo[5,1-b]thiazole (22.2 mg, 76%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662841B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-1725835fb31b42fc9ea964a47ef3d254 |
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| Source note | uspto-grants-2010_02 |
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