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HRID 428517作成日:2026年10月26日

Vinyl chloroformate → 8-(1-piperazinyl)Quinoline

https://huagongshe.com/reaction/428517

反応式

関与物質

役割名称HCID仕込み量
反応物Vinyl chloroformateHCID 78808—
反応物8-(4-Benzyl-piperazin-1-yl)quinolineHCID 18414083—
溶媒DichloromethaneHCID 6344—
生成物8-(1-piperazinyl)QuinolineHCID 11830786100.2%

反応手順

To a solution of 8-(4-benzyl-piperazin-1-yl)quinoline (2.63 g, 8.7 mmol) in methylene chloride (30 ml) was added vinyl chloroformate (1.1 ml, 13 mmol) at room temperature slowly. The reaction mixture was refluxed for 2 hours, and then concentrated under vacuum. The residue was dissolved in 12 N hydrochloric acid (20 ml) and stirred at room temperature for 1 hour. The mixture was concentrated, the residue was taken up with 40 ml ethanol and heated up to 50° C. for 2 hours. The solvent was removed under vacuum, the residue was dissolved in 1 N sodium hydroxide-ethyl acetate and extracted with ethyl acetate and washed with water. The organic layer was dried over anhydrous sodium sulfate. The solvent was removed under vacuum. Chromatography (10-30% methanol -methylene chloride plus ammonium hydroxide) afforded 1.86 g (90%) yellow oil; MS EI m/e 213 (M)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313126B1
出典データセットuspto-grants-2001_11
ORD IDord-2e55f5d3b9204febb804c6020b17ff15
出典メモuspto-grants-2001_11