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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243039Generated: October 29, 2026

Phenylboronic Acid → 1-phenyl-1H-imidazo[4,5-c]pyridine

https://huagongshe.com/reaction/243039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 178419860HCID 178419860—
CatalystCupric acetateHCID 8895—
SolventPyridineHCID 1049—
Product1-phenyl-1H-imidazo[4,5-c]pyridineHCID 5328473—
Product3-phenyl-3H-imidazo[4,5-c]pyridineHCID 68157185—

Reaction Steps

1H-Imidazo[4,5-c]pyridine (2.01 g, 0.0169 mol), copper acetate (7.66 g, 42.2 mmol) and phenyl boronic acid (5.14 g, 042.2 mmol) in pyridine (60 mL) were stirred vigorously at 37° C. in a flask open to the atmosphere for 3 days. The mixture was allowed to cool to RT then partitioned between water and DCM (3×50 mL). The combined DCM extracts were washed with water, dried (Na2SO4) and concentrated in vacuo. The residue was purified by chromatography (SiO2 0-6% (2M ammonia in methanol) in DCM) to give 1-phenyl-1H-imidazo[4,5-c]pyridine (1.60 g) and 3-phenyl-3H-imidazo[4,5-c]pyridine (1.06 g) as white solids (combined 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-3da62fae71e1414da1a87a27fd0c36a8
Source noteuspto-grants-2014_02