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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070287Generated: October 27, 2026

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

https://huagongshe.com/reaction/2070287

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 numberUS08299108B2
Source datasetuspto-grants-2012_10
ORD IDord-0cdd552959f040f2a504ece41d88bb0a
Source noteuspto-grants-2012_10