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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13485Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/13485

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPotassium CarbonateHCID 11430—
Edukt5-Fluoro-2-nitroanilineHCID 75399—
Edukt3-hydroxy-N-methylbenzamideHCID 353710—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
ProduktN-methyl{4-[3-(methylamino)-4-nitro-phenoxy](2-pyridyl))carboxamideHCID 131725842—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728010B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-6b6dff67f14a4b098baa503d8c3178a8
Quellennotizuspto-grants-2010_06