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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1611860생성일: 2026년 10월 27일

p-Hydrazinobenzenesulphonamide → Enflicoxib

https://huagongshe.com/reaction/1611860

반응식

참여 물질

역할이름HCID투입량
반응물p-HydrazinobenzenesulphonamideHCID 78105—
반응물Sodium ethoxideHCID 2723922—
반응물1,1,1-Trifluoro-4-(2,4-difluorophenyl)-3-butene-2-oneHCID 69533569—
용매EthanolHCID 702—
생성물EnflicoxibHCID 995309365%

반응 단계

In a flask with an inert atmosphere sodium ethoxide (0.53 g, 7.72 mmoles) is dissolved in 45 ml of ethanol. 1,1,1-trifluoro-4-(2,4-difluorophenyl)-3-butene-2-one (prepared according to method E-1) (0.913 g, 3.86 mmoles) and 4-(aminosulphonyl)phenylhydrazine chlorohydrate (0.87 g, 3.87 mmoles) are added and the mixture was refluxed for 16 hours. The mixture was cooled, evaporated to dryness, cold water added, and the mixture acidified by adding acetic acid and the precipitated solid filtered. This solid was redissolved in ether, treated with active C, filtered and the solvent eliminated with a rotavapor. The resulting residue was crystallised from ethyl ether-petrol ether (50:50) to give 1-(4-aminosulphonylphenyl)-5-(2,4-difluorophenyl)-4,5-dihydro-3-trifluoromethyl-1H-pyrazole (1.02 g, yield: 65%) in the form of a solid m.p.=160-2° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE038963E1
출처 데이터셋uspto-grants-2006_01
ORD IDord-35b3b07460ee4250b3e32f0a0adbd8ca
출처 메모uspto-grants-2006_01