Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095669Generated: October 25, 2026

Potassium Carbonate → 8-Bromo-2-(7-(2-methoxyethoxy)imidazo[1,2-a]pyridin-3-yl)quinoline

https://huagongshe.com/reaction/1095669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant2,8-DibromoquinolineHCID 45925951—
Reactant7-(2-Methoxyethoxy)imidazo[1,2-a]pyridineHCID 58369259—
Catalystpalladium(II) acetateHCID 167845—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product8-Bromo-2-(7-(2-methoxyethoxy)imidazo[1,2-a]pyridin-3-yl)quinolineHCID 6678156372%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2,8-dibromoquinoline (22.4 g, 78.0 mmol), 7-(2-methoxyethoxy)imidazo[1,2-a]pyridine (15.0 g, 78.0 mmol), Pd(PPh3)4 (4.51 g, 3.90 mmol), K2CO3 (21.6 g, 156 mmol) and Pd(OAc)2 (0.876 g, 3.90 mmol), dioxane (312 mL) and water (3 ml) was heated to 100° C. for 18 hours. The resulting mixture was diluted with dichloromethane (500 ml) and filtered. The filtrate was concentrated under reduced pressure and to the resulting oil was added ethyl acetate (100 ml) and methyl tert-butyl ether (100 ml). The resulting mixture was stirred overnight. Filtration to collect the resulting solids yielded the title compound (22.2 g, 72% yield). MS ESI (+) m/z 398 and 400 (M+1 of each isotope) detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138181B2
Source datasetuspto-grants-2012_03
ORD IDord-85d9d9830b824c02b2567ddfdce07f9d
Source noteuspto-grants-2012_03