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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 537941생성일: 2026년 10월 26일

Sodium Carbonate → 4-[(5E)-5-(6-fluoro-2-oxo-1,2-dihydro-3H-indol-3-ylidene)-2,2-dimethyl-2,5-dihydrofuran-3-yl]thiophene-2-carbaldehyde

https://huagongshe.com/reaction/537941

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물1,4-DioxaneHCID 31275—
반응물2-Formylthiophene-4-boronic acidHCID 11084115—
반응물(3E)-3-(4-bromo-5,5-dimethylfuran-2(5H)-ylidene)-6-fluoro-1,3-dihydro-2H-indol-2-oneHCID 58926029—
촉매HCID 178418476HCID 178418476—
용매WaterHCID 962—
생성물4-[(5E)-5-(6-fluoro-2-oxo-1,2-dihydro-3H-indol-3-ylidene)-2,2-dimethyl-2,5-dihydrofuran-3-yl]thiophene-2-carbaldehydeHCID 58926272—

반응 조건

온도80 °C

반응 단계

To 30 mL of 1,4-dioxane were added (3E)-3-(4-bromo-5,5-dimethylfuran-2(5H)-ylidene)-6-fluoro-1,3-dihydro-2H-indol-2-one (600 mg, 1.85 mmol), 5-formylthiophene-3-boronic acid (348 mg, 2.23 mmol), PdCl2(PPh3)2 (60 mg, 0.085 mmol), 1M Na2CO3 aqueous solution (7.4 mL, 7.4 mmol). The mixture was heated at 80° C. under N2 for 3.5 hours, cooled to room temperature and poured into 200 mL of water. The mixture was extracted with EtOAc (3×80 mL). The organic layers were combined, washed with brine (50 mL), dried over Na2SO4, and concentrated to give the crude product, which was purified through silica gel column with 1-5% MeOH/CHCl3 to give 4-[(5E)-5-(6-fluoro-2-oxo-1,2-dihydro-3H-indol-3-ylidene)-2,2-dimethyl-2,5-dihydrofuran-3-yl]thiophene-2-carbaldehyde as brown solid. Yield: 458 mg, 70%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865682B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-07ffcc237b7b49c5847bb242429d1fe1
출처 메모uspto-grants-2014_10