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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049234Generated: November 3, 2026

Acetamide → N-(5-((2-chloropyridin-4-yl)oxy)-6-methylpyridin-2-yl)acetamide

https://huagongshe.com/reaction/1049234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamideHCID 178—
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
ReactantHCID 90403315HCID 90403315—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Catalyst2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Solvent1,4-DioxaneHCID 31275—
ProductN-(5-((2-chloropyridin-4-yl)oxy)-6-methylpyridin-2-yl)acetamideHCID 9040258556%

Reaction Conditions

Temperature83 °C

Reaction Steps

A solution of 3-((2-chloropyridin-4-yl)oxy)-6-iodo-2-methylpyridine (8.5 g, 24.53 mmol) in dioxane (100 mL) was sparged with argon, treated with acetamide (5.07 g, 86 mmol), Cs2CO3 (11.99 g, 36.8 mmol), X-Phos (0.585 g, 1.226 mmol) and Pd2(dba)3 (1.123 g, 1.226 mmol) and heated at 83° C. for 16 h. The mixture was cooled to RT, treated with EtOAc, solids removed via filtration through diatomaceous earth, rinsed well with EtOAc, and the filtrate washed with H2O, then brine, dried over Na2SO4, concentrated to dryness and purified via silica gel chromatography (EtOAc/Hex) to afford N-(5-((2-chloropyridin-4-yl)oxy)-6-methylpyridin-2-yl)acetamide (3.8 g, 56%) as an off-white solid. MS (ESI) m/z: 278.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382228B2
Source datasetuspto-grants-2016_07
ORD IDord-7a540c3b0beb419386e69361b2edb6ea
Source noteuspto-grants-2016_07