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HRID 13485作成日:2026年10月25日

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

https://huagongshe.com/reaction/13485

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物5-Fluoro-2-nitroanilineHCID 75399—
反応物3-hydroxy-N-methylbenzamideHCID 353710—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
生成物N-methyl{4-[3-(methylamino)-4-nitro-phenoxy](2-pyridyl))carboxamideHCID 131725842—

反応条件

温度90 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728010B2
出典データセットuspto-grants-2010_06
ORD IDord-6b6dff67f14a4b098baa503d8c3178a8
出典メモuspto-grants-2010_06