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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

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl (3-aminopropyl)carbamateHCID 417669—
반응물2,4-Dichloro-3-nitroquinolineHCID 2785138—
용매TriethylamineHCID 8471—
생성물4-[3-(Benzyloxycarbonylamino)propylamino]-2-chloro-3-nitroquinolineHCID 1878396684.8%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06069149
출처 데이터셋uspto-grants-2000_05
ORD IDord-84d058dba5b743769543c5eb60a6f701
출처 메모uspto-grants-2000_05