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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591043Generated: October 31, 2026

N-bromobutanimide → HCID 70819495, compound

https://huagongshe.com/reaction/591043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 70819501HCID 70819501—
SolventEthanolHCID 702—
ProductHCID 70819495HCID 7081949590.2%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238026B2
Source datasetuspto-grants-2016_01
ORD IDord-b8c0fee9572247e58b320a62185f8827
Source noteuspto-grants-2016_01