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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 630509생성일: 2026년 10월 27일

Potassium Carbonate → (1-(5-(5-Ethoxy-2-fluorophenyl)pyrimidin-2-yl)-3-(methylsulfinyl)-1H-indol-6-yl)(morpholino)methanone

https://huagongshe.com/reaction/630509

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물5-Ethoxy-2-fluorophenylboronic Acid (contains varying amounts of Anhydride)HCID 16217468—
반응물(1-(5-Bromopyrimidin-2-yl)-3-(methylsulfinyl)-1H-indol-6-yl)(morpholino)methanoneHCID 118666026—
용매WaterHCID 962—
용매2-Methyl-2-butanolHCID 6405—
생성물(1-(5-(5-Ethoxy-2-fluorophenyl)pyrimidin-2-yl)-3-(methylsulfinyl)-1H-indol-6-yl)(morpholino)methanoneHCID 118666101—

반응 조건

온도90 °C

반응 단계

Potassium carbonate (0.185 g, 1.34 mmol) and (Ataphos)2PdCl2 (0.032 g, 0.044 mmol) were added under an argon atmosphere to a solution of (1-(5-bromopyrimidin-2-yl)-3-(methylsulfinyl)-1H-indol-6-yl)(morpholino)methanone (0.2 g, 0.445 mmol) and 2-fluoro-5-ethoxyphenylboronic acid (0.165 g, 0.89 mmol) in tert-amylalcohol (8.0 mL) and water (0.8 mL). The reaction mixture was stirred at 90° C. for 4 h, then cooled to ambient temperatures and filtered over celite. The filtrate was concentrated and the residue purified by flash column chromatography [silica; dichloromethane with 2% methanol]. White solid. Yield: 0.14 g (62% of theory)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09315490B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-ca89d940355443719bba7dae908d69f2
출처 메모uspto-grants-2016_04