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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 366316생성일: 2026년 10월 25일

Dimethylformamide → 3-(4-Chloro-2-ethyl-6-fluorobenzofuran-7-yl)-1-amino-6-trifluoromethyluracil

https://huagongshe.com/reaction/366316

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물O-(2,4-dinitrophenyl)hydroxylamineHCID 87140—
반응물3-(4-Chloro-2-ethyl-6-fluorobenzofuran-7-yl)-6-trifluoromethyluracilHCID 23289176—
용매WaterHCID 962—
생성물3-(4-Chloro-2-ethyl-6-fluorobenzofuran-7-yl)-1-amino-6-trifluoromethyluracilHCID 2328916558%

반응 조건

온도65 °C

반응 단계

80 ml of N,N-dimethylformamide was added to 3.4 g (9.0 mmol) of 3-(4-chloro-2-ethyl-6-fluorobenzofuran-7-yl)-6-trifluoromethyluracil, 2.7 g (14 mmol) of 2,4-dinitrophenoxyamine and 5.0 g (36 mmol) of potassium carbonate, followed by stirring at 60 to 70° C. for 1 hour. After completion of the reaction, the reaction solution was poured into water and extracted with ethyl acetate. The organic layer was washed sequentially with water and a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. Then, the obtained residue was purified by silica gel column chromatography to obtain 2.0 g (yield: 58%) of the desired product as white crystals. Melting point: 145-147° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06130187
출처 데이터셋uspto-grants-2000_10
ORD IDord-6b136cb4a742421583c4eabc5cf768e4
출처 메모uspto-grants-2000_10