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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Bromo-2-(4-chlorophenyl)imidazo[1,2-a]pyridine | HCID 828291 | — |
| Reactant | (2-Fluoro-3-formylphenyl)boronic acid | HCID 16217829 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 86651935 | HCID 86651935 | 56.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148370B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-089286299dae47038d6a6827b80c9220 |
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| Source note | uspto-grants-2012_04 |
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