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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 633514생성일: 2026년 10월 26일

Cesium fluoride → 7-methoxy-3-(2-phenoxyphenyl)-1H-pyrrolo[2,3-c]pyridine

https://huagongshe.com/reaction/633514

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참여 물질

역할이름HCID투입량
반응물Cesium fluorideHCID 25953—
반응물(2-Phenoxyphenyl)boronic acidHCID 2773559—
반응물3-Iodo-7-methoxy-1H-pyrrolo[2,3-c]pyridineHCID 53412719—
촉매HCID 178418397HCID 178418397—
용매MethanolHCID 887—
생성물7-methoxy-3-(2-phenoxyphenyl)-1H-pyrrolo[2,3-c]pyridineHCID 9041667338.6%

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온도120 °C

반응 단계

A mixture of 3-iodo-7-methoxy-1H-pyrrolo[2,3-c]pyridine (0.274 g, 1.0 mmol), 2-phenoxyphenylboronic acid (0.278 g, 1.3 mmol, 1.3 equivalents), Pd(PPh3)4 (0.058 g, 0.05 mmol), and cesium fluoride (0.456 g, 3 mmol) in dimethxoyethane (3 mL) and methanol (1.5 mL) was heated under microwave conditions (120° C., 30 minutes). The reaction mixture was partitioned between water and ethyl acetate. The aqueous layer was extracted three times with ethyl acetate. The combined organic layers were washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated. The residue was purified by flash column chromatography (silica gel, 30% ethyl acetate/hexanes) to give the title compound (0.122 g, 38.6% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09321764B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-c490091761d54383a603ffe9a2da55ae
출처 메모uspto-grants-2016_04