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HRID 1434584作成日:2026年10月25日

4-Bromo-1,2-dichlorobenzene → 1-(3,4-Dichloro-phenyl)-4-[4-(3-Piperidin-1-yl-propoxy)-phenyl]piperazine

https://huagongshe.com/reaction/1434584

反応式

関与物質

役割名称HCID仕込み量
反応物4-Bromo-1,2-dichlorobenzeneHCID 29013—
反応物Binap, (A+-)-HCID 634876—
反応物1-[4-(3-Piperidin-1-ylpropoxy)phenyl]piperazineHCID 9924013—
反応物Sodium t-butoxideHCID 23676156—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物1-(3,4-Dichloro-phenyl)-4-[4-(3-Piperidin-1-yl-propoxy)-phenyl]piperazineHCID 57935744—

反応手順

Tris(dibenzylidineacetone) di palladium (0) (5 mol %; 23 mg) was added to a mixture of 1-[4-(3-piperidin-1-yl-propoxy)-phenyl]-piperazine (D11) (150 mg; 0.49 mmol), 3,4-dichloro bromo benzene (160 mg; 1.2 eq), sodium tert-butoxide (71 mg; 1.1 eq) and racemic 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (7.5 mol %; 24 mg) in dry toluene (3 ml). The resulting mixture was heated at reflux under argon for 18 hours. The reaction was allowed to cool to room temperature and diluted with ethyl acetate (10 ml). The resulting solids were removed by filtration and the filtrate evaporated in vacuo. The residue was purified by column chromatography on silica eluting with 3% methanol in dichloromethane to afford the title compound as a buff solid (45 mg)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07615550B2
出典データセットuspto-grants-2009_11
ORD IDord-d0f9f1e5b5ed42eabc20fea828ac68be
出典メモuspto-grants-2009_11