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HRID 1017432作成日:2026年10月25日

1-Methylpiperazine → 1-Methyl-4-(5-nitropyridin-2-yl)piperazine

https://huagongshe.com/reaction/1017432

反応式

関与物質

役割名称HCID仕込み量
反応物1-MethylpiperazineHCID 53167—
反応物2-Chloro-5-nitropyridineHCID 78308—
溶媒TetrahydrofuranHCID 8028—
生成物1-Methyl-4-(5-nitropyridin-2-yl)piperazineHCID 2764066—

反応手順

To a solution of 20 g (126 mmol) of 2-chloro-5-nitropyridine in 200 ml tetrahydrofuran were added dropwise 35 ml (315 mmol) 1-methylpiperazine within 10 min. The reaction mixture was refluxed for additional 1.5 h. After cooling to room temperature, the solvent was removed in vacuo and the residue was re-dissolved in 200 ml ethyl acetate. The organic phase was washed with 200 ml 1 N sodium bicarbonate solution, dried (magnesium sulfate) and evaporated to give 27.9 g (quantitative) of the title compound as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06479483B2
出典データセットuspto-grants-2002_11
ORD IDord-920ccf5cf0d14e50aebba20a95d672ad
出典メモuspto-grants-2002_11