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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33285생성일: 2026년 10월 23일

3-Formylphenylboronic acid → 2-(3-formylphenyl)-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indol-6-one

https://huagongshe.com/ko/reaction/33285

반응식

참여 물질

역할이름HCID투입량
반응물3-Formylphenylboronic acidHCID 2734356—
반응물2-Phenyl-3,10-diazatricyclo[6.4.1.04,13]trideca-1,4,6,8(13)-tetraen-9-oneHCID 10220882—
생성물2-(3-formylphenyl)-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indol-6-oneHCID 11109037—

반응 단계

In a manner similar to that described above for Compound 12, the tricyclic bromide (381 mg, 1.44 mmol) and 3-formylbenzeneboronic acid (345 mg, 2.16 mmol) were coupled to yield 2-(3-formylphenyl)-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indol-6-one 15, 346 mg (83%), as a tan solid. 1H NMR (300 MHz, d6-DMSO) δ 2.86 (m, 2H), 3.16 (m, 2H), 7.01 (t, 1H, J=7.8 Hz), 7.34 (d, 1H, J=7.3 Hz), 7.50 (m, 2H), 7.73 (m, 2H), 7.85 (br t, 1H), 7.94 (s, 1H), 9.88 (s, 1H), 11.50 (br s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429578B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-78bfd41320b34608984971ff0c153670
출처 메모uspto-grants-2008_09