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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13485생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물5-Fluoro-2-nitroanilineHCID 75399—
반응물3-hydroxy-N-methylbenzamideHCID 353710—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
생성물N-methyl{4-[3-(methylamino)-4-nitro-phenoxy](2-pyridyl))carboxamideHCID 131725842—

반응 조건

온도90 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728010B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-6b6dff67f14a4b098baa503d8c3178a8
출처 메모uspto-grants-2010_06