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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446662Generated: October 25, 2026

Potassium Carbonate → 4-(7-Chloro-imidazo[1,2-a]pyridin-3-yl)-phenylamine

https://huagongshe.com/reaction/1446662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734620—
Reactant7-Chloro-3-iodoimidazo[1,2-a]pyridineHCID 57497697—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
Product4-(7-Chloro-imidazo[1,2-a]pyridin-3-yl)-phenylamineHCID 68539411100%

Reaction Steps

To a round bottomed flask add 7-chloro-3-iodo-imidazo[1,2-a]pyridine (3.0 g, 0.011 mol), add 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (2.6 g, 1.1 equiv.), potassium carbonate (4.5 g, 3 equiv.), dioxane (40 mL), and water (20 mL). Deoxygenate this mixture thoroughly with N2 then add dichlorobis(triphenylphosphine)palladium (II) (0.23 g, 0.03 equiv.) and reflux the reaction overnight under N2. Concentrate the reaction to dryness and slurry in DCM. Filter this slurry thru Celite® and wash with DCM. Concentrate the filtrate then purify by silica plug (EtOAc to 5% MeOH: DCM to 10% MeOH: DCM) to give a pale grey solid (2.6 g, 100%). MS (ES), m/z 244 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666879B2
Source datasetuspto-grants-2010_02
ORD IDord-6b0cbc677db84ef98bfb4419ea8b46ae
Source noteuspto-grants-2010_02