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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 345663생성일: 2026년 10월 24일

Arcyriarubin A → 3,4-bis(1H-indol-3-yl)-2,5-dihydro-1H-pyrrol-2-one

https://huagongshe.com/ko/reaction/345663

반응식

참여 물질

역할이름HCID투입량
반응물Arcyriarubin AHCID 2399—
반응물Aluminium lithium hydrideHCID 21226445—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물3,4-bis(1H-indol-3-yl)-2,5-dihydro-1H-pyrrol-2-oneHCID 532765018.3%

반응 조건

온도0 °C

반응 단계

20 ml of a 1M solution of LiAlH4 in diethyl ether was added to a solution of 1.0 g of 3,4-bis(3-indolyl)-1H-pyrrole-2,5-dione in 140 ml of THF. The mixture was stirred for 18 hours under nitrogen. The mixture was cooled to 0° C., quenched with 50 ml of water, then acidified to pH 2 with 2M hydrochloric acid and extracted with ethyl acetate. The organic extracts were washed with saturated sodium bicarbonate solution, dried and evaporated. The residue was purified on silica gel with 5-10% methanol in dichloromethane. The first product eluted was triturated with ethyl acetate/hexane to give 175 mg of 3,4-bis(3-indolyl)-3-pyrrolin-2-one, m.p. 290°-293° C. (decomposition). The second product eluted was crystallized from ethyl acetate/chloroform to give 490 mg of 5-hydroxy-3,4-bis(3-indolyl)-3-pyrrolin-2-one, m.p. above 250° C. (decomposition).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05057614
출처 데이터셋uspto-grants-1991_10
ORD IDord-4f5b573773694b3ca8ac6ab6160a6328
출처 메모uspto-grants-1991_10