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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915617Generated: October 25, 2026

Potassium Carbonate → 4-(4-amino-3-nitrophenoxy)-N-methylpicolinamide

https://huagongshe.com/reaction/1915617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-N-methylpicolinamideHCID 1476814—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant4-Amino-3-NitrophenolHCID 3758882—
SolventDimethylformamideHCID 6228—
Product4-(4-amino-3-nitrophenoxy)-N-methylpicolinamideHCID 17756497—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture containing 4-amino-3-nitrophenol (1 eq) and potassium bis(trimethylsilyl)amide (2 eq) was stirred in dimethylformamide for 2 hours at room temperature. To this mixture was added (4-chloro(2-pyridyl))-N-methylcarboxamide (1 eq) and potassium carbonate (1.2 eq) and stirred at 90° C. for 3 days. The reaction mixture was then concentrated and partitioned between ethyl acetate and water. The organic layer was separated and washed with brine, dried, filtered, and concentrated in vacuum to give brown solid. Purification on silica gel (2% triethyl amine/50% ethyl acetate in hexane) gave 4-[(4-amino-3-nitrophenyl)oxy]-N-methylpyridine-2-carboxamide as an orange solid. The product gave satisfactory NMR. HPLC, 3.39 min; MS: MH+=289.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614330B2
Source datasetuspto-grants-2013_12
ORD IDord-3e51a4f80d3b4c75b4885ecbaf067912
Source noteuspto-grants-2013_12