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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cadaverine | HCID 273 | — |
| 반응물 | Chloroform | HCID 6212 | — |
| 반응물 | Indeno(1,2-c)isochromene-5,11-dione | HCID 265728 | — |
| 생성물 | 6-(5-aminopentyl)-5,6-dihydro-5,11-diketo-11H-indeno[1,2-c]isoquinoline hydrochloride | HCID 16221201 | 82% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08829022B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-1896206c22c64f498a32c3cc73760910 |
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| 출처 메모 | uspto-grants-2014_09 |
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