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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28955생성일: 2026년 10월 24일

Sodium Bicarbonate → 3-(4-Bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)benzaldehyde

https://huagongshe.com/ko/reaction/28955

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참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물3-Formylphenylboronic acidHCID 2734356—
반응물4-Bromo-2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridineHCID 46907955—
촉매HCID 178418397HCID 178418397—
용매DimethylformamideHCID 6228—
생성물3-(4-Bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)benzaldehydeHCID 7301403877%

반응 조건

온도100 °C

반응 단계

In a sealed pressure tube was added 4-bromo-2-iodo-1-phenylsulfonyl-1H-pyrrolo[2,3-b]pyridine (2.1 mmol; preparation disclosed in WO03/000690A1), 3-formylbenzeneboronic acid (2.1 mmol), N,N-dimethylformamide (15 mL), aqueous saturated sodium bicarbonate (5 mL) and tetrakis(triphenylphosphine)palladium(0) (0.1 mmol). The reaction was purged with nitrogen, capped and stirred at 100° C. for 16 h. After cooling to room temperature the reaction was concentrated under vacuum, taken up in ethyl acetate, washed with water, brine, dried over sodium sulfate, filtered and evaporated to dryness under vacuum. Purification by flash chromatography by silica gel (0-4% ethyl acetate in methylene chloride) gave the title compound as a white solid (77%). ESMS [M+H]+: 441.2

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419988B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-9173d86765b646f184635d085c57b10c
출처 메모uspto-grants-2008_09