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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521547Generated: October 26, 2026

1,10-Phenanthroline → 2-(5-Bromo-2-pyridinyl)benzoxazole

https://huagongshe.com/reaction/521547

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,10-PhenanthrolineHCID 1318—
ReactantCesium carbonateHCID 10796—
Reactant2-BromoanilineHCID 11992—
Reactant5-Bromo-pyridine-2-carbonyl chlorideHCID 19090771—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product2-(5-Bromo-2-pyridinyl)benzoxazoleHCID 4694161330%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-bromoaniline (3.90 g, 22.7 mmol), 5-bromopyridine-2-carbonyl chloride (5.00 g, 22.7 mmol), Cs2CO3 (14.78 g, 45.36 mmol), 1,10-phenanthroline (0.409 g, 2.27 mmol), CuI (0.216 g, 1.13 mmol) and anhydrous 1,4-dioxane (40 mL) was degassed with argon for about 40 min while stirring. The stirring reaction mixture was then maintained under argon at about 120° C. for about 40 h. Upon completion, the reaction was cooled to RT and poured over CH2Cl2 (300 mL). The organics were then washed with sat. NaHCO3, H2O and brine, dried over MgSO4, filter and concentrated in vacuo. Purification of the crude product via flash chromatography (SiO2, 4:1 dichloromethane-hexanes) and subsequent recrystallization from hexanes afforded compound 11 (1.86 g, 30% yield) as colorless fibers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328086B2
Source datasetuspto-grants-2016_05
ORD IDord-3c0af32c96b544d6aa712ca19029fe13
Source noteuspto-grants-2016_05