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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 366717생성일: 2026년 10월 26일

Tetrahydrofuran → (Z)-3-[(4-Acetyl-1H-pyrrol-2-yl)methylene]-1,3-dihydro-5-fluoro-4-iodo-2H-indol-2-one

https://huagongshe.com/reaction/366717

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물5-Fluoro-4-iodoindolin-2-oneHCID 9795601—
반응물4-Acetyl-1H-pyrrole-2-carboxaldehydeHCID 12415110—
용매IsopropanolHCID 3776—
용매PiperidineHCID 8082—
생성물(Z)-3-[(4-Acetyl-1H-pyrrol-2-yl)methylene]-1,3-dihydro-5-fluoro-4-iodo-2H-indol-2-oneHCID 18366029—

반응 단계

1,3-Dihydro-5-fluoro-4-iodo-2H-indol-2-one (0.77 g, 2.8 mmol) (see Example 2A, supra) and 4-acetyl-2-formylpyrrole (0.42 g, 3.06 mmol) (Example 90A above) were suspended in 1% piperidine in 2-propanol (12 mL) and THF (5 mL) and heated at 85° C. for 2 h. Yellow precipitate was formed. After cooling to room temperature, product was collected by filtration and washed with aqueous 2-propanol and dried in vacuum oven to yield (Z)-3-[(4-Acetyl-1H-pyrrol-2-yl)methylene]-1,3-dihydro-5-fluoro-4-iodo-2H-indol-2-one. (Yield 0.89 g, 80.8%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06130239
출처 데이터셋uspto-grants-2000_10
ORD IDord-8347d42534b7420ebcb35dbc39a80a94
출처 메모uspto-grants-2000_10