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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1357102생성일: 2026년 10월 27일

Citric Acid → 2-bromo-3-(5-methyl-1H-indol-3-yl)-N-methylmaleimide

https://huagongshe.com/reaction/1357102

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물5-MethylindoleHCID 11978—
반응물2,3-Dibromo-N-methylmaleimideHCID 18155—
반응물HCID 178418443HCID 178418443—
용매TetrahydrofuranHCID 8028—
생성물2-bromo-3-(5-methyl-1H-indol-3-yl)-N-methylmaleimideHCID 988351086.8%

반응 조건

온도40 °C

반응 단계

To a solution of 5-methylindole (90 mg, 0.78 mmol) dissolved in THF (3 mL) was added 0.95M ethylmagnesium bromide (0.83 mL, 0.78 mmol) at 40° C., and the whole was stirred at 40° C. for 45 minutes. Successively, thereto was added a solution of 2,3-dibromo-N-methylmaleimide (100 mg, 0.39 mmol) dissolved in THF (5 mL), followed by stirring under heating and refluxing for 3 hours. After 20% aqueous citric acid solution (1 mL) was added thereto under ice cooling and the whole was stirred, THF was removed by concentration under reduced pressure and the resulting concentrate was extracted with ethyl acetate. The extract was dried over sodium sulfate and then concentrated under reduced pressure. The residue was purified by column chromatography over silica gel (ethyl acetate:n-hexane=1:1) to obtain 2-bromo-3-(5-methyl-1H-indol-3-yl)-N-methylmaleimide (108 mg, 86.3%) as red solids.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06589977B1
출처 데이터셋uspto-grants-2003_07
ORD IDord-ee1861e7df8a4453a81ee0ed5030694f
출처 메모uspto-grants-2003_07