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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7014생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/7014

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Sodium AcetateHCID 517045—
반응물5-Bromo-2-fluorobenzonitrileHCID 2724900—
반응물(spiro[cyclopentane-1,3'-[3H]indol]-2'(1'H)-one-5-yl)boronic acidHCID 21986244—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물5'-(3-cyano-4-fluorophenyl)-spiro[cyclopentane-1,3'-[3H]indol]-2'(1'H)-oneHCID 5424349810.5%

반응 단계

A solution of 3-cyano-4-fluoro-bromobenzene (0.63 g, 3.1 mmol), and tetrakis(triphenylphosphine)palladium(0) (0.2 g) in ethylene glycol dimethyl ether (20 cm3) was stirred under N2 for 20 minutes. To this mixture was then added (spiro[cyclopentane-1,3′-[3H]indol]-2′(1′H)-one-5-yl) boronic acid (1.0 g, 4.7 mmol) and sodium acetate (1.0 g, 9.4 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 (0.10 g, 10%) as white crystals. mp: 264–266° C.; 1H NMR (DMSO-d6) δ 10.4 (s, 1H), 8.3 (dd, 1H, J=2.4, 3.7 Hz), 8.1–8.0 (m, 1H), 7.6–7.5 (m, 2H), 7.5 (dd, 1H, J=1.9, 6.3 Hz), 6.9 (d, 1H, J=8.1 Hz), 2.0–1.9 (m, 8H); MS [M−H]−=305.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084168B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b5da18c4b6b945759ba515164e6f2ac3
출처 메모uspto-grants-2006_08