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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1936949생성일: 2026년 10월 24일

Sodium Hydroxide → 5'-(4-Cyano-3-fluorophenyl)-spiro[cyclohexane-1,3'-[3H]indol]-2'(1'H)-one

https://huagongshe.com/ko/reaction/1936949

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Sodium AcetateHCID 517045—
반응물4-Bromo-2-fluorobenzonitrileHCID 736029—
반응물(spiro[cyclohexane-1,3'-[3H]indol]-2'(1'H)-one-5-yl)boronic acidHCID 21986219—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물5'-(4-Cyano-3-fluorophenyl)-spiro[cyclohexane-1,3'-[3H]indol]-2'(1'H)-oneHCID 2201934637%

반응 단계

A solution of 4-cyano-3-fluoro-bromobenzene (0.76 g, 3.8 mmol), and tetrakis(triphenylphosphine)palladium(0) (0.3 g) in ethylene glycol dimethyl ether (15 cm3) was stirred under N2 for 20 minutes. To this mixture was then added (spiro[cyclohexane-1,3′-[3H]indol]-2′(1′H)-one-5-yl) boronic acid (1.4 g, 5.7 mmol) and sodium acetate (1.2 g, 11.4 mmol) in water (5 cm3). The solution was brought to reflux for 18 hours and then cooled to room temperature, poured into 2N NaOH and extracted with EtOAc (×3). The combined extracts were washed with water, brine, dried (MgSO4), and evaporated. The residue was purified by column chromatography (SiO2, EtOAc, hexane) to afford the title compound (0.45 g, 37%) as an off-white solid. mp: 258-260° C.; 1H NMR (DMSO-d6) δ8.8 (s, 1H), 7.7-7.6 (m, 2H), 7.5 (td, 2H, J=0.9. 1.5, 5.7 Hz), 7.4 (dd, 1H, J=1.5, 8.8 Hz), 7.0 (d, 1H, J=8.1 Hz), 2.0-1.6 (m, 10H); MS (−)APCI [M−H]− @ m/z 319.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06391907B1
출처 데이터셋uspto-grants-2002_05
ORD IDord-05737275ea4e4e039b2fe66eb62b0cdb
출처 메모uspto-grants-2002_05