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HRID 374145作成日:2026年10月25日
3-Pyridinecarboximidic acid, N-cyano-, 1-methylethyl ester → N-cyano-N'-(3-nitroxypropyl)-3-pyridinecarboximidamide
https://huagongshe.com/reaction/374145
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3-Pyridinecarboximidic acid, N-cyano-, 1-methylethyl ester | HCID 10081201 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 反応物 | 3-Nitroxypropylamine nitrate | HCID 22014591 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | N-cyano-N'-(3-nitroxypropyl)-3-pyridinecarboximidamide | HCID 10399794 | 39% |
反応手順
Isopropyl N-cyano-3-pyridinecarboximidate (0.50 g, 2.6 mmol) was dissolved in methanol (10 ml), and 3-nitroxypropylamine nitrate (0.53 g, 2.9 mmol) and sodium methoxide (0.16 g, 2.9 mmol) were added. The mixture was stirred at room temperature for 18 hours. After the reaction was completed, the reaction solution was concentrated under reduced pressure, and the residue was extracted with chloroform (30 ml×3). The chloroform layer was washed with water (100 ml), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The concentrated residue thus obtained was subjected to chromatography on a silica gel column (WAKO GEL C-200, 30 g) eluting with chloroform-methanol (60:1). Eluted fractions were concentrated under reduced pressure and crystallized from methanol-diethyl ether to give the title compound (0.26 g, 1.0 mmol, yield: 39%) as colorless crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05166347 |
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| 出典データセット | uspto-grants-1992_11 |
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| ORD ID | ord-d14fe50d3e4047a8a3e294f045a77354 |
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| 出典メモ | uspto-grants-1992_11 |
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