Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290168Generated: October 28, 2026

N-bromobutanimide → 3-Bromo-8-(2,6-dichloro-3-nitrobenzyloxy)-2-methylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1290168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant8-(2,6-Dichloro-3-nitrobenzyloxy)-2-methylimidazo[1,2-a]pyridineHCID 10807891—
SolventEthanolHCID 702—
Solvent1,4-DioxaneHCID 31275—
Product3-Bromo-8-(2,6-dichloro-3-nitrobenzyloxy)-2-methylimidazo[1,2-a]pyridineHCID 1179691681.7%

Reaction Steps

To a solution of 8-(2,6-dichloro-3-nitrobenzyloxy)-2-methylimidazo[1,2-a]pyridine (85 mg) in a mixture of ethanol (1 ml) and 1,4-dioxane (1 ml) was added in one portion N-bromosuccinimide (43 mg) at ambient temperature. After stirring for one hour at the same temperature, the mixture was filtered to give 3-bromo-8-(2,6-dichloro-3-nitrobenzyloxy)-2-methylimidazo[1,2-a]pyridine (85 mg) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750699
Source datasetuspto-grants-1998_05
ORD IDord-c5981572d077437fabb923b717ef4c45
Source noteuspto-grants-1998_05