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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235540Generated: October 27, 2026

N-Bromosuccinamide → 2-Bromo-N,N-dipropylimidazo[1,2-a]pyridin-5-amine

https://huagongshe.com/reaction/2235540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BromosuccinamideHCID 9834204—
ReactantHCID 68581368HCID 68581368—
SolventDimethylformamideHCID 6228—
Product2-Bromo-N,N-dipropylimidazo[1,2-a]pyridin-5-amineHCID 6858199049%

Reaction Conditions

Temperature0 °C

Reaction Steps

N,N-Dipropylimidazo[1,2-a]pyridin-5-amine (1.0 g, 4.6 mmol) was diluted in DMF (25 mL). The solution was cooled to 0° C. N-bromosuccinamide (0.83 g, 4.7 mmol) was added. After 5 minutes, the reaction was quenched with water. The solution was extracted with ether, dried, and concentrated. Flash chromatography (40% EtOAc/hexanes) gave the title compound as a yellow oil which solidified upon overnight freezing at −20° C. 0.67 g obtained (49% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714009B2
Source datasetuspto-grants-2010_05
ORD IDord-7e629ca5076c4bcc8ebce8796c5d40c8
Source noteuspto-grants-2010_05