関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzyl (3-aminopropyl)carbamate | HCID 417669 | — |
| 反応物 | 2,4-Dichloro-3-nitroquinoline | HCID 2785138 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | 4-[3-(Benzyloxycarbonylamino)propylamino]-2-chloro-3-nitroquinoline | HCID 18783966 | 84.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06069149 |
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| 出典データセット | uspto-grants-2000_05 |
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| ORD ID | ord-84d058dba5b743769543c5eb60a6f701 |
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| 出典メモ | uspto-grants-2000_05 |
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