戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 359509作成日:2026年10月25日

Hydride → 1-(2-Methyl-5-pyrazinylmethyl)-2-(nitromethylene)imidazolidine

https://huagongshe.com/reaction/359509

反応式

関与物質

役割名称HCID仕込み量
反応物HydrideHCID 166653—
反応物2-(Nitromethylene)imidazolidineHCID 3014763—
反応物2-(Chloromethyl)-5-methylpyrazineHCID 13221025—
反応物HCID 178418361HCID 178418361—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物1-(2-Methyl-5-pyrazinylmethyl)-2-(nitromethylene)imidazolidineHCID 18460023%

反応条件

温度40 °C

反応手順

2-Nitromethyleneimidazolidine (12.9 g) was dissolved in dry dimethylformamide (100 ml), and at room temperature 60% oily soldium hydride (4.4 g) was added. The mixture was stirred at room temperature until the generation of hydrogen ceased. Then, 2-methyl 5-pyrazinylmethyl chloride (14.3 g ) was added at room temperature, and the mixture was stirred at 40° C. for 8 hours. After cooling to room temperature, the reaction mixture was added to 200 ml of water, and extracted with dichloromethane. On distilling off dichloromethane from the organic layer under reduced pressure, 1-(2-methyl-5-pyrazinylmethyl)-2-(nitromethylene)imidazolidine (5.4 g) was obtained as yellow crystals having a melting point of 163° to 166° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05001138
出典データセットuspto-grants-1991_03
ORD IDord-4b011944a2a14252be6c6900cc7ae6c6
出典メモuspto-grants-1991_03