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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1501423생성일: 2026년 10월 27일

Ethanol → 4-(1-benzothien-2-yl)-1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1501423

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물TolueneHCID 1140—
반응물Benzo(B)Thiophene-2-Boronic AcidHCID 2359—
반응물Potassium CarbonateHCID 11430—
반응물4-bromo-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2,3-b]pyridineHCID 57477561—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물4-(1-benzothien-2-yl)-1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridineHCID 5748041387.6%

반응 조건

온도120 °C

반응 단계

1-Benzothien-2-ylboronic acid (0.05 g, 0.0003 mol) and 4-bromo-1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridine (0.10 g, 0.00031 mol) were combined in toluene (3.0 mL, 0.028 mol) and ethanol (1.0 mL, 0.017 mol). Potassium carbonate (0.085 g, 0.00062 mol) dissolved in water (1.0 mL) then was added and the reaction was degassed with nitrogen. Then tetrakis(triphenylphosphine)palladium(0) (0.05 g, 0.00004 mol) was added and the reaction was heated to 120° C. in a sealed tube in the microwave for 60 minutes. This was allowed to cool to rt, taken up in ethyl acetate and washed with water 2×, brine, dried over magnesium sulfate and concentrated to give 4-(1-benzothien-2-yl)-1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]-pyridine (0.10 gm) as an oil, LC/MS (M+H)+ 381.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09206187B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-e9b4d56cb1ec442e8c172eb7d4a1193f
출처 메모uspto-grants-2015_12