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HRID 269877作成日:2026年10月27日

Phenethyl bromide → 2-[4-(3-Cyclohexylpropyl)piperazin-1-yl]-5-methoxybenzonitrile

https://huagongshe.com/reaction/269877

反応式

関与物質

役割名称HCID仕込み量
反応物Phenethyl bromideHCID 7666—
反応物1-(4-Methoxyphenyl)-piperazine, dihydrochlorideHCID 2723700—
反応物3-Cyclohexylpropyl methanesulfonateHCID 23111443—
反応物5-Methoxy-2-(piperazin-1-yl)benzonitrileHCID 23111446—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物2-[4-(3-Cyclohexylpropyl)piperazin-1-yl]-5-methoxybenzonitrileHCID 2311151346.6%

反応手順

Production Example 1 was repeated except that 1-(4-methoxyphenyl)piperazine dihydrochloride, (2-bromoethyl)benzene and tetrahydrofuran were replaced with 5-methoxy-2-(piperazin-1-yl)benzonitrile (599 mg), 3-cyclohexylpropyl methylsulfonate (608 mg) and N,N-dimethylformamide (6.8 mL), respectively, and the resulting crude product was purified on silica gel column chromatograpy (eluent, ethyl acetate: hexane=1:1) to provide 2-[4-(3-cyclohexylpropyl)piperazin-1-yl]-5-methoxybenzonitrile (439 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07449466B2
出典データセットuspto-grants-2008_11
ORD IDord-bf18d2e7c17e4b388881331306289aa6
出典メモuspto-grants-2008_11