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HRID 28821作成日:2026年10月23日

Tributylvinyltin → Tert-butyl 4-[2-(1-hydroxycyclohexyl)-2-(3-vinylphenyl)ethyl]piperazine-1-carboxylate

https://huagongshe.com/ja/reaction/28821

反応式

関与物質

役割名称HCID仕込み量
反応物TributylvinyltinHCID 81998—
反応物Tert-butyl 4-[2-(3-bromophenyl)-2-(1-hydroxycyclohexyl)ethyl]piperazine-1-carboxylateHCID 68852390—
触媒HCID 178418397HCID 178418397—
溶媒TolueneHCID 1140—
生成物Tert-butyl 4-[2-(1-hydroxycyclohexyl)-2-(3-vinylphenyl)ethyl]piperazine-1-carboxylateHCID 6885568690%

反応手順

A mixture of tert-butyl 4-[2-(3-bromophenyl)-2-(1-hydroxycyclohexyl)ethyl]piperazine-1-carboxylate (see Example 135, step 2) (141 mg, 0.300 mmol), tributyl(vinyl)tin (114 mg, 0.360 mmol, 1.2 equivalent), and tetrakis(triphenylphosphine)palladium (17 mg, 0.015 mmol, 5 mol %) in toluene (3 mL) was heated at reflux under nitrogen until all starting material was consumed and precipitation of black palladium occurred (1-2 h). Filtration through Celite® and purification via flash column chromatography (silica, gradient from 0% ethyl acetate/hexane to 10% ethyl acetate/hexane) yielded 111 mg (90%) tert-butyl 4-[2-(1-hydroxycyclohexyl)-2-(3-vinylphenyl)ethyl]piperazine-1-carboxylate as a viscous colorless oil. MS (ES) m/z 415.4 ([M+H]+); HRMS: calcd for C25H38N2O3, 414.2882; found (ESI), 415.2966.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419980B2
出典データセットuspto-grants-2008_09
ORD IDord-c1a5468414bb40a68540044f156d5906
出典メモuspto-grants-2008_09