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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555987Generated: October 27, 2026

Water → 6-(6-Methoxy-3-pyridinyl)imidazo[1,2-a]pyridin-2-amine

https://huagongshe.com/reaction/555987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant(6-Methoxypyridin-3-yl)boronic acidHCID 2734368—
ReactantN-{6-bromoimidazo[1,2-a]pyridin-2-yl}-2,2,2-trifluoroacetamideHCID 12065953—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product6-(6-Methoxy-3-pyridinyl)imidazo[1,2-a]pyridin-2-amineHCID 66986015—

Reaction Steps

N-(6-Bromo-imidazo[1,2-a]pyridin-2-yl)-2,2,2-trifluoro-acetamide (Intermediate A1, step 3) (0.84 g, 2.72 mmol), 2-methoxy-5-pyridineboronic acid (0.50 g, 3.27 mmol) and dry 1,4-dioxane (10 ml) are placed in a microwave vial and purged with Argon. Pd(PPh3)4 (0.16 g, 0.14 mmol) is added followed by a solution of Cs2CO3 in water (2.66 g, 8.16 mmol in 3 ml). The reaction mixture is heated using microwave radiation at 150° C. for 45 minutes and then left overnight at room temperature. The mixture is filtered through Celite® (filter agent) and washed through with EtOAc (100 ml). The organic filtrate is washed with NaHCO3 (50 ml) and brine (50 ml), dried over MgSO4, filtered and concentrated in vacuo. Purification by flash chromatography on silica eluting with MeOH in DCM (1% increasing to 10%) affords the title compound. [MH+241.07].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053574B2
Source datasetuspto-grants-2011_11
ORD IDord-b286b40771ef48668e1d3353bbd08baf
Source noteuspto-grants-2011_11