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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626502Generated: October 30, 2026

Propionamide → N-(4-((2-methyl-6-nitropyridin-3-yl)oxy)pyridin-2-yl)propionamide

https://huagongshe.com/reaction/626502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropionamideHCID 6578—
ReactantCesium carbonateHCID 10796—
Reactant3-((2-Chloropyridin-4-yl)oxy)-2-methyl-6-nitropyridineHCID 90403621—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Catalyst2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Solvent1,4-DioxaneHCID 31275—
ProductN-(4-((2-methyl-6-nitropyridin-3-yl)oxy)pyridin-2-yl)propionamideHCID 9041028574%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of Example A3 (0.50 g, 1.882 mmol), propionamide (0.550 g, 7.53 mmol), Cs2CO3 (0.920 g, 2.82 mmol), and X-phos (0.045 g, 0.094 mmol) in dioxane (10 mL) was sparged with Ar, treated with Pd2(dba)3 (0.086 g, 0.094 mmol), sparged again with Ar and heated at 90° C. for 20 h. The mixture was cooled to RT, treated with EtOAc and the solids removed via filtration. The filtrate was washed with brine, dried over Na2SO4, concentrated to dryness and purified via silica gel chromatography (EtOAc/DCM) to afford N-(4-((2-methyl-6-nitropyridin-3-yl)oxy)pyridin-2-yl)propionamide (420 mg, 74%). MS (ESI) m/z: 303.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309224B2
Source datasetuspto-grants-2016_04
ORD IDord-0ff586d31f0a4a8195adc8d348eaf4a4
Source noteuspto-grants-2016_04