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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1257590생성일: 2026년 10월 27일

Tetrahydrofuran → 1-benzenesulfonyl-N-4-cyclohexyl-1H-pyrrolo[2,3-b]pyridine-4,5-diamine

https://huagongshe.com/reaction/1257590

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참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물(1-benzenesulfonyl-5-nitro-1H-pyrrolo[2,3-b]pyridin-4-yl)-cyclohexyl-amineHCID 67343455—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물1-benzenesulfonyl-N-4-cyclohexyl-1H-pyrrolo[2,3-b]pyridine-4,5-diamineHCID 67322397103.8%

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온도50 °C

반응 단계

A suspension of (1-benzenesulfonyl-5-nitro-1H-pyrrolo[2,3-b]pyridin-4-yl)-cyclohexyl-amine (10 g, 25.0 mmol) and palladium on carbon (2.7 g, 10%, wet, Degussa, E101 NE/W) in a 3:1 mixture of THF and ethanol (200 ml) was stirred under a hydrogen atmosphere (2-3 balloons) at 50° C. for 13 h. The reaction mixture was cooled to 25° C. then was filtered through Celite. The filtrate was concentrated under reduced pressure to afford crude 1-benzenesulfonyl-N-4-cyclohexyl-1H-pyrrolo[2,3-b]pyridine-4,5-diamine (9.61 g, 100%) as a rose foam. LCMS (Method G, ESI): RT=0.83 min, m+H=371.2. This material was used in subsequent reactions without additional purification or characterization.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08461328B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-a55e68ae36ec4955a745a55093070871
출처 메모uspto-grants-2013_06