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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1960357생성일: 2026년 10월 25일

2-Trifluoromethylbenzenesulphonyl chloride → ethyl 7-({[2-(trifluoromethyl)phenyl]sulfonyl}amino)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1960357

반응식

참여 물질

역할이름HCID투입량
반응물2-Trifluoromethylbenzenesulphonyl chlorideHCID 136616—
반응물1H-Indole-2-carboxylic acid, 7-amino-, ethyl esterHCID 11138194—
용매PyridineHCID 1049—
생성물ethyl 7-({[2-(trifluoromethyl)phenyl]sulfonyl}amino)-1H-indole-2-carboxylateHCID 5747617888.2%

반응 단계

To a mixture of ethyl 7-amino-1H-indole-2-carboxylate (4.1 g) and pyridine (60 ml) was added 2-trifluoromethylbenzenesulfonyl chloride (5.0 g) under ice-cooling, and the mixture was stirred from under ice-cooling to room temperature for 18 hr. The reaction mixture was concentrated, and the residue was diluted with ethyl acetate. The solution was washed with aqueous citric acid solution and saturated brine, and filtrated through silica gel. The eluate was concentrated under reduced pressure, and the obtained pale-brown oil was crystallized from ethyl acetate-hexane to give the title compound (7.3 g, yield 88%) as pale-brown crystals. MS: 413(MH+). melting point: 138-139° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08410087B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-065c0478d1fd41e28838e9bfb4ce1d9c
출처 메모uspto-grants-2013_04