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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684907Generated: October 25, 2026

6-Bromo-2-(4-chlorophenyl)imidazo[1,2-a]pyridine → HCID 86651935, compound

https://huagongshe.com/reaction/1684907

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-2-(4-chlorophenyl)imidazo[1,2-a]pyridineHCID 828291—
Reactant(2-Fluoro-3-formylphenyl)boronic acidHCID 16217829—
CatalystHCID 178418397HCID 178418397—
ProductHCID 86651935HCID 8665193556.8%

Reaction Conditions

Temperature70 °C

Reaction Steps

500 mg of 6-bromo-2-(4-chlorophenyl)imidazo[1,2-a]pyridine, 473 mg of 2-fluoro-3-formylbenzeneboronic acid and 93 mg of tetrakis(triphenylphosphine)palladium are placed under a stream of argon in a round-bottomed flask comprising a mixture, degassed beforehand under a stream of argon, of 5 ml of acetonitrile, 5 ml of toluene and 6 ml of a 2M sodium carbonate solution. The reaction mixture is heated at 70° C. for 21 h. After cooling, the reaction mixture is diluted with ethyl acetate and water and then the organic phase is separated, dried and evaporated under reduced pressure. The residue is purified by chromatography on silica gel, elution being carried out with a dichloromethane/ethyl acetate 98/02 mixture. 324 mg of compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148370B2
Source datasetuspto-grants-2012_04
ORD IDord-089286299dae47038d6a6827b80c9220
Source noteuspto-grants-2012_04