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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33298생성일: 2026년 10월 24일

4-(Trifluoromethyl)phenylboronic acid → 2-(4-Trifluoromethyl-phenyl)-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one

https://huagongshe.com/ko/reaction/33298

반응식

참여 물질

역할이름HCID투입량
반응물4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
반응물2-Phenyl-3,10-diazatricyclo[6.4.1.04,13]trideca-1,4,6,8(13)-tetraen-9-oneHCID 10220882—
생성물2-(4-Trifluoromethyl-phenyl)-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-oneHCID 11078020—

반응 단계

In a manner analogous to the method described above for Compound 12, the tricyclic bromide (300 mg, 1.13 mmol) and 4-trifluoromethylphenylboronic acid (322 mg, 1.70 mmol) were coupled to yield 2-(4-trifluoromethyl-phenyl)-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one, 261 mg (70%), as an off-white solid. mp 208-209° C.; 1H NMR (300 MHz, d6-DMSO) δ 3.09 (m, 2H), 3.40 (m, 2H), 7.27 (app t, 1H, J=7.8 Hz), 7.60 (dd, 1H, J=8.1, 0.9 Hz), 7.71 (dd, 1H, J=7.5, 0.6 Hz), 7.88 (m, 4H), 8.13 (br t, 1H), 11.77 (br s, 1H); MS (FAB, MH+) 331; Anal. (C18H13F3N2O.1.0 H2O) C, H, N.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429578B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-f1eda020169d46eba1ae4e6f573ecd5a
출처 메모uspto-grants-2008_09