Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1108624생성일: 2026년 10월 26일
Benzyl (3-aminopropyl)carbamate → 4-[3-(Benzyloxycarbonylamino)propylamino]-2-chloro-3-nitroquinoline
https://huagongshe.com/reaction/1108624
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzyl (3-aminopropyl)carbamate | HCID 417669 | — |
| 반응물 | 2,4-Dichloro-3-nitroquinoline | HCID 2785138 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | 4-[3-(Benzyloxycarbonylamino)propylamino]-2-chloro-3-nitroquinoline | HCID 18783966 | 84.8% |
반응 단계
0.19 g (0.768 mmol) of 2,4-dichloro-3-nitroquinoline and 0.16 g (0.768 mmol) of N-(benzyloxycarbonyl)-1,3-propanediamine was heated at 70° C. in 5 ml of triethylamine for one hour with stirring. After triethylamine was distilled off under reduced pressure, the residue was dissolved in methylene chloride, washed with water, and dried (MgSO4). The solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=2:1 (v/v)) to obtain 0.27 g (0.651 mmol) of 4-[3-(benzyloxycarbonylamino)propylamino]-2-chloro-3-nitroquinoline shown below as yellow powder. ##STR29## Its spectroscopic data are as follows: 1H-NMR (CDCl3) δ (ppm) :1.79 (2H, m), 3.35 (4H, m), 5.02 (1H, br), 5.18 (2H, s), 7.15 (1H, br), 7.37 (5H, m), 7.57 (1H, t, J=8.0 Hz), 7.73 (1H, t, J=7.8 Hz), 7.90 (1H, d, J=8.4 Hz), 8.21 (1H, d, J=8.0 Hz).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06069149 |
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| 출처 데이터셋 | uspto-grants-2000_05 |
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| ORD ID | ord-84d058dba5b743769543c5eb60a6f701 |
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| 출처 메모 | uspto-grants-2000_05 |
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