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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

反応式

関与物質

役割名称HCID仕込み量
反応物3-Pyridinecarboximidic acid, N-cyano-, 1-methylethyl esterHCID 10081201—
反応物Sodium MethoxideHCID 10942334—
反応物3-Nitroxypropylamine nitrateHCID 22014591—
溶媒MethanolHCID 887—
生成物N-cyano-N'-(3-nitroxypropyl)-3-pyridinecarboximidamideHCID 1039979439%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05166347
出典データセットuspto-grants-1992_11
ORD IDord-d14fe50d3e4047a8a3e294f045a77354
出典メモuspto-grants-1992_11