HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591043Generated: October 31, 2026
N-bromobutanimide → HCID 70819495, compound
https://huagongshe.com/reaction/591043
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 70819501 | HCID 70819501 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 70819495 | HCID 70819495 | 90.2% |
Reaction Steps
To a solution of methyl 2-(tert-butoxy)-2-{imidazo[1,2-a]pyridin-2-yl}acetate (25c) (108 mg, 0.41 mmol) in ethanol (5 mL) at 0° C. was added N-bromosuccinimide (76 mg, 0.43 mmol) portionwise. The mixture was stirred at 0° C. for 15 minutes and concentrated in vacuo. The residue was dissolved in ethyl acetate (5 mL) and washed with a saturated solution of sodium hydrogencarbonate (2×5 mL). The organic layer was dried over sodium sulfate and concentrated in vacuo to provide the desired product (25d) (127 mg, 0.37 mmol, 90%) as a yellow oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238026B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-b8c0fee9572247e58b320a62185f8827 |
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| Source note | uspto-grants-2016_01 |
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