関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methane | HCID 297 | — |
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 2-Nitroimidazole | HCID 10701 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 1-(2,3-Epoxypropyl)-2-nitroimidazole | HCID 334973 | — |
| 反応物 | 2-Fluoroethylazanium chloride | HCID 139190533 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 1-(2-Nitro-1-imidazolyl)-3-(2-fluoroethylamino)-2-propanol hydrochloride | HCID 14621553 | — |
反応手順
A mixture of 1-(2,3-epoxypropyl)-2-nitroimidazole prepared by the method described by Beaman et al. [Beaman, A. G., Tautz, W. and Duschinsky, R., 1968; Studies in the Nitroimidazole Series. III, Antimicrobial Agents and Chemotherapy, pp. 520-530] (4.00 g, 23.7 mmol), 2-fluoroethylammonium chloride (5.00 g, 50.2 mmol) and sodium hydroxide (2.00 g, 50.0 mmol) in ethanol (60 cm3) was stirred at 15° C. for 30 minutes then heated under reflux for 3 hours. The reaction mixture was then treated with decolourising charcoal (0.5 g), cooled and filtered. Concentration under reduced pressure afforded a pale yellow oil which was dissolved in ethanol (20 cm3) and treated with a small excess of anhydrous ethereal hydrogen chloride to give 1-(2-nitro-1-imidazolyl)-3-(2-fluoroethylamino)-2-propanol hydrochloride in the form of a pale yellow crystalline solid (4.38 g, 68.9%) after recrystallisation from aqueous ethanol, m.p. 178°-179° C. (dec.) after drying in vacuo.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05521203 |
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| 出典データセット | uspto-grants-1996_05 |
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| ORD ID | ord-aad602478b2e4dea9c6031becbaa3645 |
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| 出典メモ | uspto-grants-1996_05 |
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