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HRID 32165作成日:2026年10月25日

2-Chloroethyl methyl sulfide → 1-(2-Methylsulfanylethyl)-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine

https://huagongshe.com/reaction/32165

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloroethyl methyl sulfideHCID 10965—
反応物Potassium CarbonateHCID 11430—
反応物1-[2-(3,3,5,5-Tetramethylcyclohexyl)phenyl]piperazineHCID 11992284—
溶媒AcetonitrileHCID 6342—
生成物1-(2-Methylsulfanylethyl)-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazineHCID 2314278570.5%

反応条件

温度80 °C

反応手順

A mixture of the 1-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine (100 mg, 0.333 mmol) produced in Example (8b), 2-chloroethyl methyl sulfide (38.7 mg, 0.349 mmol), potassium carbonate (78.2 mg, 0.566 mmol) and acetonitrile (2 mL) was stirred for 8 hours and 30 minutes at an external temperature of 80° C. The reaction mixture was concentrated and the resultant residue was purified by NH silica gel column chromatography (ethyl acetate/heptane) to give 88 mg of 1-(2-methylsulfanylethyl)-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine as a colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425554B2
出典データセットuspto-grants-2008_09
ORD IDord-bd9582084aa347fba5c296a15048dd4a
出典メモuspto-grants-2008_09