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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437467Generated: November 1, 2026

Toluene → 2-(3-methoxyphenyl)-6-phenyl-1H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/1437467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
ReactantPhenyl dihydrogen orthoborateHCID 78412—
Reactant6-bromo-2-(3-methoxyphenyl)-1H-imidazo[4,5-b]pyridineHCID 23025807—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventTetrahydrofuran ethyl acetateHCID 21939870—
Product2-(3-methoxyphenyl)-6-phenyl-1H-imidazo[4,5-b]pyridineHCID 994830466.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

Under an argon stream, a mixture of 6-bromo-2-(3-methoxyphenyl)-1H-imidazo[4,5-b]pyridine (Compound of Reference Example 2) (21.3 g), phenylboric acid (22.2 g), tetrakis(triphenylphosphine)palladium(0) (7.60 g), 2 M sodium carbonate (175 ml), toluene (525 ml) and tetrahydrofuran (175 ml) was stirred at 90° C. for 24 hours. The reaction mixture was distributed into ethyl acetate-tetrahydrofuran (3:1, v/v) and water. The organic layer was washed with water, dried over MgSO4. The solvent was distilled off under reduced pressure, and the resulting crystals were collected by filtration to obtain 2-(3-methoxyphenyl)-6-phenyl-1H-imidazo[4,5-b]pyridine (14.0 g, 66%). The crystals were recrystallized from chloroform-methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622479B2
Source datasetuspto-grants-2009_11
ORD IDord-77b3acd212ef4075a35f01050660df0d
Source noteuspto-grants-2009_11