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HRID 1588547作成日:2026年10月27日

Isopropyl N-cyano-4-pyridinecarboximidate → N-cyano-N'-(3-nitroxypropyl)-4-pyridinecarboximidamide

https://huagongshe.com/reaction/1588547

反応式

関与物質

役割名称HCID仕込み量
反応物Isopropyl N-cyano-4-pyridinecarboximidateHCID 10012715—
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)-4-pyridinecarboximidamideHCID 1003767641.5%

反応手順

Isopropyl N-cyano-4-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 (0.22 g, 4.1 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. The residual concentrate was extracted with chloroform (50 ml×3). The chloroform layer was washed with water (100 ml), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residual concentrate was subjected to chromatography on a silica gel column (WAKO GEL C-200, 50 g) eluting with chloroform-methanol (60:1). The eluted fractions were concentrated under reduced pressure and crystallized from methanol-diethyl ether to give the title compound (0.27 g, 1.08 mmol, yield: 41%) as colorless crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05223508
出典データセットuspto-grants-1993_06
ORD IDord-557829bc603b4402bce8c49fb1dde4af
出典メモuspto-grants-1993_06