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HRID 1108624作成日:2026年10月26日

Benzyl (3-aminopropyl)carbamate → 4-[3-(Benzyloxycarbonylamino)propylamino]-2-chloro-3-nitroquinoline

https://huagongshe.com/reaction/1108624

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl (3-aminopropyl)carbamateHCID 417669—
反応物2,4-Dichloro-3-nitroquinolineHCID 2785138—
溶媒TriethylamineHCID 8471—
生成物4-[3-(Benzyloxycarbonylamino)propylamino]-2-chloro-3-nitroquinolineHCID 1878396684.8%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06069149
出典データセットuspto-grants-2000_05
ORD IDord-84d058dba5b743769543c5eb60a6f701
出典メモuspto-grants-2000_05