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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 731989생성일: 2026년 10월 26일

p-Anisoyl chloride → 4-[(3-fluoro-6-methylphenanthridin-5(6H)-yl)carbonyl]phenol

https://huagongshe.com/reaction/731989

반응식

참여 물질

역할이름HCID투입량
반응물p-Anisoyl chlorideHCID 7477—
반응물TriethylamineHCID 8471—
반응물1-[2-(2,4-Difluorophenyl)phenyl]ethan-1-amineHCID 22482376—
반응물N-[1-(2',4'-difluoro-1,1'-biphenyl-2-yl)ethyl]-4-methoxybenzamideHCID 68815187—
용매HexaneHCID 8058—
용매tert-Butyl methyl etherHCID 15413—
생성물4-[(3-fluoro-6-methylphenanthridin-5(6H)-yl)carbonyl]phenolHCID 11580798—

반응 단계

N-[1-(2′,4′-difluoro-1,1′-biphenyl-2-yl)ethyl]-4-methoxybenzamide—The title compound was prepared from 4-methoxybenzoyl chloride (731 mg, 4.28 mmol), 1-(-2′,4′-difluoro-biphenyl-2-yl)-ethylamine (1 g, 4.28 mmol), and triethylamine (717 uL, 5.1 mmol) according to the procedure and in the same manner as described in Example 33, step c. The product was isolated from a Biotage® (40 Mi) column for flash column chromatography (5-30% methyl tert-butylether in hexane) resulting in the isolation of a white solid, 1.53 g (97%). mp 134.5-135° C.; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.29 (d, J=5.43 Hz, 3 H) 3.80 (s, 3 H) 4.96 (m, J=5.95 Hz, 1 H) 6.97 (d, J=9.05 Hz, 2 H) 7.18 (m, 2 H) 7.36 (m, 3 H) 7.64 (d, J=4.14 Hz, 2 H) 7.83 (d, J=7.50 Hz, 2 H) 8.66 (s, 1 H); MS (ESI) m/z 368 ([M+H]+); Anal. calcd for C22H19F2NO2: C:71.92 H:5.21 N:3.81 Found: C:72.11 H:5.23 N:3.77

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07585871B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-3f2ccc82aa80439f8eb29f9c9b3dd79a
출처 메모uspto-grants-2009_09