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HRID 2251799作成日:2026年10月25日

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

https://huagongshe.com/reaction/2251799

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US07320979B2
出典データセットuspto-grants-2008_01
ORD IDord-2dbce81032684078acf47967ca21d03c
出典メモuspto-grants-2008_01