戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 444956作成日:2026年10月26日

Potassium Carbonate → 1-Allyl-4-(5-nitropyridin-2-yl)piperazine

https://huagongshe.com/reaction/444956

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2-Chloro-5-nitropyridineHCID 78308—
反応物1-AllylpiperazineHCID 806422—
溶媒DimethylformamideHCID 6228—
生成物1-Allyl-4-(5-nitropyridin-2-yl)piperazineHCID 6914601823%

反応手順

2.0 g (12.61 mmol) of 2-chloro-5-nitropyridine were dissolved in 8 ml of dimethylformamide, and 3.49 g (25.23 mmol) of potassium carbonate were added. After that, a solution of 1.75 g (13.88 mmol) of N-allylpiperazine in 2 ml of dimethylformamide was added slowly dropwise to the reaction mixture (exothermic reaction). The reaction mixture was then stirred at room temperature for 2 hours. After the solvent had been concentrated down to dryness, the resulting residue was stirred up in 100 ml of heptane. The precipitate which remained was filtered off with suction. The filtrate was concentrated, resulting in 720 mg of the title compound. The precipitate which had been filtered off with suction was treated with 150 ml of water and extracted three times with diethyl ether. The organic phase was washed with a saturated solution of sodium chloride and dried over sodium sulfate. A further 2.24 g of the title compound were isolated after the solvent had been filtered and concentrated down to dryness. The total yield of 1-allyl-4-(5-nitropyridin-2-yl)piperazine was 2.96 g (95% of theory).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08476275B2
出典データセットuspto-grants-2013_07
ORD IDord-1119197eb4604e688ab7ec14b9f75cbd
出典メモuspto-grants-2013_07