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HRID 431435생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/431435

반응식

참여 물질

역할이름HCID투입량
반응물PiperazineHCID 4837—
반응물2-Acetyl-6-methoxynaphthaleneHCID 77506—
반응물LithiumHCID 3028194—
생성물1-[6-(Piperazin-1-yl)naphthalen-2-yl]ethan-1-oneHCID 15398671—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06660530B2
출처 데이터셋uspto-grants-2003_12
ORD IDord-deaa9b0a4aae4aa296572d54c6a593c7
출처 메모uspto-grants-2003_12