돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33320생성일: 2026년 10월 23일

1-Octanol → 6-oxo-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indole-2-carboxylic acid octyl ester

https://huagongshe.com/ko/reaction/33320

반응식

참여 물질

역할이름HCID투입량
반응물1-OctanolHCID 957—
반응물TriethylamineHCID 8471—
반응물2-Iodo-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-oneHCID 9883223—
반응물6-Oxo-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indole-2-carboxylic acid methyl esterHCID 10220471—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매DimethylformamideHCID 6228—
생성물6-oxo-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indole-2-carboxylic acid octyl esterHCID 18339992—

반응 단계

Following a procedure similar to that described for Example MM (Compound 42), 2-iodo-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one (330 mg, 1.06 mmol), triethylamine (342 mg, 3.38 mmol), and palladium tetrakis(triphenylphosphine) (61 mg, 0.05 mmol) were reacted in 20 mL 1:1 n-octanol:DMF in a sealed tube under a carbon monoxide atmosphere to yield 6-oxo-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indole-2-carboxylic acid octyl ester, 250 mg (58%), as a white solid: m.p. 170-171° C.; 1H NMR (300 MHz, d6-DMSO) δ 0.85 (t, J=7.2 Hz, 3H), 1.27 (m, 8H), 1.42 (m, 2H), 1.73 (m, 2H), 3.25 (m, 2H), 3.42 (m, 2H), 4.30 (t, J=6.6 Hz, 3H), 7.38 (app t, J=7.5 Hz, 1H), 7.62 (dd, J=8.1, 0.9 Hz, 1H), 7.74 (dd, J=7.5, 0.9 Hz, 1H), 8.17 (br t, 1H), 11.86 (br s, 1H). MS (FAB, MH+) 343. Anal. (C20H26N2O3) C, H, N.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429578B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-024a55adefad437b95ff0724fa5643df
출처 메모uspto-grants-2008_09