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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13485Generated: October 25, 2026

Dimethylformamide → N-methyl{4-[3-(methylamino)-4-nitro-phenoxy](2-pyridyl))carboxamide

https://huagongshe.com/reaction/13485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Fluoro-2-nitroanilineHCID 75399—
Reactant3-hydroxy-N-methylbenzamideHCID 353710—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ProductN-methyl{4-[3-(methylamino)-4-nitro-phenoxy](2-pyridyl))carboxamideHCID 131725842—

Reaction Conditions

Temperature90 °C

Reaction Steps

The mixture containing 5-fluoro-2-nitrophenylamine (1 eq), Potassium bis(trimethylsilyl)amide (2 eq) was stirred in dimethylformamide for 2 hours at room temperature. To this mixture was added (3-hydroxyphenyl)-N-methylcarboxamide (1 eq) and Potassium carbonate (1.2 eq) and stirred at 90° C. for 16 h. 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 gave N-methyl{4-[3-(methylamino)-4-nitro-phenoxy](2-pyridyl))carboxamide. It was taken in methanol and hydrogenated with catalytic amount of 10% Pd/C to give {4-[4-amino-3-(methylamino)phenoxy](2-pyridyl)}-N-methylcarboxamide. MS: MH+=272.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728010B2
Source datasetuspto-grants-2010_06
ORD IDord-6b6dff67f14a4b098baa503d8c3178a8
Source noteuspto-grants-2010_06