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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1994790생성일: 2026년 10월 25일

Methyl iodide → ethyl 7-(methyl{[2-(trifluoromethyl)phenyl]sulfonyl}amino)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1994790

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물HexaneHCID 8058—
반응물Potassium CarbonateHCID 11430—
반응물ethyl 7-({[2-(trifluoromethyl)phenyl]sulfonyl}amino)-1H-indole-2-carboxylateHCID 57476178—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물ethyl 7-(methyl{[2-(trifluoromethyl)phenyl]sulfonyl}amino)-1H-indole-2-carboxylateHCID 5913558072%

반응 단계

To a solution of ethyl 7-({[2-(trifluoromethyl)phenyl]sulfonyl}amino)-1H-indole-2-carboxylate (5.0 g) and potassium carbonate (2.0 g) in N,N-dimethylformamide (50 mL) was added methyl iodide (0.75 mL) under ice-cooling, and the mixture was stirred from under ice-cooling to room temperature for 18 hr. The reaction solution was ice-cooled, methyl iodide (0.75 mL) was added again, and the mixture was stirred from under ice-cooling to room temperature for 18 hr. The reaction solution was diluted with ethyl acetate, washed with water, aqueous citric acid solution and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was subjected to basic silica gel column chromatography (ethyl acetate:hexane=20:80-35:65), and the obtained crude product was subjected three times to silica gel column chromatography (ethyl acetate:hexane=5:95-10:90) to give the title compound (3.7 g, yield: 72%) as a pale-yellow oil. MS: 427 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07652133B2
출처 데이터셋uspto-grants-2010_01
ORD IDord-08f687149d484c998603081a5369acca
출처 메모uspto-grants-2010_01