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HRID 25861作成日:2026年10月26日

o-Bromocumene → 1-(3-Benzyl-phenyl)-2-(S)-isopropyl-4-(2-isopropyl-phenyl)-piperazine

https://huagongshe.com/reaction/25861

反応式

関与物質

役割名称HCID仕込み量
反応物o-BromocumeneHCID 23475—
反応物Dimethoxyethane ethanolHCID 20074477—
反応物4-(3'-Benzylphenyl)-3-(S)-isopropyl-piperazineHCID 20760004—
反応物Sodium t-butoxideHCID 23676156—
触媒2'-(diphenylphosphanyl)-N,N-dimethyl-[1,1'-biphenyl]-2-amineHCID 2734939—
溶媒TolueneHCID 1140—
溶媒Diethyl EtherHCID 3283—
生成物1-(3-Benzyl-phenyl)-2-(S)-isopropyl-4-(2-isopropyl-phenyl)-piperazineHCID 6912955562.2%

反応条件

温度80 °C

反応手順

110.7 mg (0.38 mmol) 4-(3′-Benzylphenyl)-3-(S)-isopropyl-piperazine (88a), 123.5 mg (0.62 mmol, 1.65 eq.) 1-Bromo-2-isopropyl-benzene 11.7 mg (12.7 μmol, 0.034 eq.) Pd2(dba)3, 7.4 mg (19.3 μmol, 0.05 eq.) 2-Diphenylphosphino-2′-dimethylamino-biphenyl and 87.3 mg (0.91 mmol, 2.42 eq.) NaOt-Bu were dissolved in 5 ml dry toluene. The resulting mixture was heated under N2 at 80° C. for 15.5 h. After cooling to room temperature the mixture was diluted with ether and washed with brine. The comb. org. fractions were dried over Na2SO4 and evaporated. Column chromatography (hexanes/EtOAc (9+1)) yielded 96.5 mg (0.23 mmol, 62.20%) 1-(3-Benzyl-phenyl)-2-(S)-isopropyl-4-(2-isopropyl-phenyl)-piperazine (89) as a clear oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858600B2
出典データセットuspto-grants-2005_02
ORD IDord-1b122892a0f943948cd06552bfdb562e
出典メモuspto-grants-2005_02