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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 859126생성일: 2026년 10월 27일

Hydrochloric Acid → 3-bromo-4-(1H-indol-3-yl)-1-methyl-pyrrole-2,5-dione

https://huagongshe.com/reaction/859126

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IndoleHCID 798—
반응물2,3-Dibromo-N-methylmaleimideHCID 18155—
반응물Lithium HexamethyldisilazideHCID 2733832—
용매TetrahydrofuranHCID 8028—
생성물3-bromo-4-(1H-indol-3-yl)-1-methyl-pyrrole-2,5-dioneHCID 9796502—

반응 단계

A solution of 1.445 g of indole dissolved in 29 ml of dry tetrahydrofliran is brought to from −20 to −10° C. under argon, and then 26 ml of LiHMDS (1M in hexane) are added dropwise in the course of 15 minutes. After 45 minutes at −10° C., the solution is diluted with an additional 15 ml of tetrahydrofuran and a solution of 2 g of N-methyl-2,3-dibromomaleimide dissolved in 17 ml of tetrahydrofuran is added dropwise in the course of 30 minutes. After 15 minutes at −10° C. and 15 minutes at 0° C., the reaction is stopped by the addition, at 0° C., of 50 ml of a 0.3N hydrochloric acid solution. The reaction mixture is extracted with ethyl acetate, and the organic phases are washed with a saturated NaCl solution, dried over MgSO4 and then evaporated under reduced pressure. The desired product is precipitated using methanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07151108B2
출처 데이터셋uspto-grants-2006_12
ORD IDord-8d71644fca2846b59ac06d95e5ee4419
출처 메모uspto-grants-2006_12