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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 582255생성일: 2026년 10월 24일

4-Fluoroaniline → N-(4-Fluorophenyl)-6-[3-(trifluoromethyl)phenoxy]pyrazine-2-carboxamide

https://huagongshe.com/ko/reaction/582255

반응식

참여 물질

역할이름HCID투입량
반응물4-FluoroanilineHCID 9731—
반응물Sodium CarbonateHCID 10340—
반응물2-Chloro-6-[3-(trifluoromethyl)phenoxy]pyrazineHCID 21266842—
촉매(+/-)-1-[2-(Diphenylphosphino)ferrocenyl]ethyl-di-tert-butylphosphineHCID 76007372—
촉매HCID 178418476HCID 178418476—
용매O-XyleneHCID 7237—
생성물N-(4-Fluorophenyl)-6-[3-(trifluoromethyl)phenoxy]pyrazine-2-carboxamideHCID 2126684165.3%

반응 단계

Analogously to Example 3, 25 mmol of 2-chloro-6-[3-(trifluoromethyl)phenoxy]pyrazine (prepared according to U.S. Pat. No. 4,254,125, Example 21), 27.5 mmol of 4-fluoroaniline, 2.92 g (27.5 mmol) of sodium carbonate, 17.5 mg (25 μmol) of dichlorobis(triphenylphosphine)palladium(II) and 0.31 g (0.75 mmol) of (±)-1-[2-(diphenylphosphino)-ferrocenyl]ethyl-di-tert-butylphosphine in 25 ml of xylene were reacted under a CO pressure of 17 bar at 120° C. for 21 hours. The composition of the dissolved products in the xylene phase was determined by GC. 65.3 percent of the title compound (amide) and 34.7 percent of by-product (secondary amine) were found. The amide was isolated by column chromatography and purified. Data concerning the title product was:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05922870
출처 데이터셋uspto-grants-1999_07
ORD IDord-6430dfcc27fc4d51822ec38a44870022
출처 메모uspto-grants-1999_07