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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72840생성일: 2026년 10월 24일

Cadaverine → 6-(5-aminopentyl)-5,6-dihydro-5,11-diketo-11H-indeno[1,2-c]isoquinoline hydrochloride

https://huagongshe.com/ko/reaction/72840

반응식

참여 물질

역할이름HCID투입량
반응물CadaverineHCID 273—
반응물ChloroformHCID 6212—
반응물Indeno(1,2-c)isochromene-5,11-dioneHCID 265728—
생성물6-(5-aminopentyl)-5,6-dihydro-5,11-diketo-11H-indeno[1,2-c]isoquinoline hydrochlorideHCID 1622120182%

반응 단계

Benz[d]indeno[1,2-b]pyran-5,11-dione (4d) (0.100 g, 0.403 mmol) was treated with 1,5-diaminopentane (0.206 g, 2.014 mmol) in CHCl3 (40 mL) and the reaction mixture was heated at reflux for 16 h. The reaction mixture was allowed to cool to room temperature and washed with water (3×15 mL). The solution was dried over sodium sulfate, filtered, and treated with 2 M HCl in Et2O (5 mL). After 30 min, the reaction mixture was filtered and the filter pad was washed with CHCl3 (50 mL) and hexanes (50 mL) to provide an orange solid (0.122 g, 82%): mp 265-268° C. IR (film) 3432, 3077, 2856, 1707, 1635, 1611, 1549, and 1504 cm−1; 1H NMR (CDCl3) δ 8.59 (d, J=8.1 Hz, 1H), 8.23 (d, J=8.1 Hz, 1H), 7.85-7.80 (m, 3H), 7.74 (d, J=7.4 Hz, 1H), 7.63-7.51 (m, 4H), 4.52 (t, J=7.3 Hz, 2H), 2.81 (m, 2H), 1.83 (m, 2H) 1.65-1.52 (m, 4H); ESIMS m/z (rel intensity) 333 (MH+, 100). Anal. (C21H21ClN2O2.0.75H2O) C, H, N.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829022B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-1896206c22c64f498a32c3cc73760910
출처 메모uspto-grants-2014_09