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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1180913생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/1180913

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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 번호US07282588B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-c3b5ed7fca7e40c2900dc865fb3a161f
출처 메모uspto-grants-2007_10