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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1994789생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1994789

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 번호US07652133B2
출처 데이터셋uspto-grants-2010_01
ORD IDord-1610d74c26854347b0a5242d28f25b99
출처 메모uspto-grants-2010_01