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HRID 431435作成日:2026年10月27日

Piperazine → 1-[6-(Piperazin-1-yl)naphthalen-2-yl]ethan-1-one

https://huagongshe.com/reaction/431435

反応式

関与物質

役割名称HCID仕込み量
反応物PiperazineHCID 4837—
反応物2-Acetyl-6-methoxynaphthaleneHCID 77506—
反応物LithiumHCID 3028194—
生成物1-[6-(Piperazin-1-yl)naphthalen-2-yl]ethan-1-oneHCID 15398671—

反応手順

Anhydrous piperazine (7 g, 81.3 mmol; dried in a vacuum desiccator over KOH-drierite mixture for 3 days) was dissolved in a mixture of dry, freshly distilled toluene and hexamethyl phosphoric amide (HMPA), 25 mL each. To the solution was added 556 mg (80.1 mmol) of lithium rod, cut in small pieces under argon atmosphere, and the mixture was stirred under argon for 24 hours, during which time all lithium has dissolved. Vacuum-dried 1-(6-methoxy-2-naphthyl)-1-ethanone (prepared as described in Arsenijevic et al., Org. Synth. Coll. 1988 6:34-36, the disclosure of which is incorporated herein by reference) (3.5 g, 17.5 mmol) was added, and stirring was continued for additional 65 hours. After quenching with 300 mL of water, extraction with dichloromethane (3×300 mL), drying with anhydrous magnesium sulfate, and evaporation, a mixture of white and yellow solids was obtained. Extraction with 300 mL of hot methanol gave raw product, 1-(6-piperazino-2-naphthyl)-1-ethanone, which was purified by column chromatography (70-230 mesh silica, 25×120 mm, 5% methanol in dichloromethane). The yield was 1.54 g (35%). After recrystallization from ethyl acetate, the sample melted at 170.5-172° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06660530B2
出典データセットuspto-grants-2003_12
ORD IDord-deaa9b0a4aae4aa296572d54c6a593c7
出典メモuspto-grants-2003_12