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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746822Generated: November 1, 2026

1,10-Phenanthroline → HCID 9904298, compound

https://huagongshe.com/reaction/746822

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,10-PhenanthrolineHCID 1318—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-(1H-pyrrol-3-yl)pyridineHCID 820397—
ReactantHCID 69303602HCID 69303602—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 9904298HCID 9904298—

Reaction Conditions

Temperature110 °C

Reaction Steps

A solution of 2-(1H-pyrrol-3-yl)pyridine (0.144 g, 1.0 mmol), 3-(3-iodophenyl)pyridine (0.281 g, 1.2 mmol), 1,10-phenanthroline (0.360 g, 2 mmol), Potassium phosphate (0.445 g, 2.1 mmol), in dioxane (3 mL) was degassed with argon for 5 minutes, followed by the addition of copper (I) iodide (0.038 g, 0.2 mmol). The reaction mixture was heated at 110° C. for 4 hr. The reaction mixture was quenched with H2O (30 mL), then extracted with EtOAc (3×30 mL) and the combined organic extracts washed with brine. The organic phase was dried over Na2SO4 and concentrated in vacuo. The crude purified by liquid chromatography on silica gel using an ISCO single channel system (Hexane/EtOAc=9/1 to 1/9) to afford 2-[1-(3-pyridin-3-ylphenyl)-1H-pyrrol-3-yl]pyridine as a slightly yellow oil. The free base in anhydrous diethyl ether was treated with 1.5 equivalents HCl (1M in ether) to give the HCl salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393959B2
Source datasetuspto-grants-2008_07
ORD IDord-fe335ee6e0654b1180dfcf4b9c764b28
Source noteuspto-grants-2008_07