戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 971371作成日:2026年10月24日

Tri-o-tolylphosphine → 4-(3'-Benzylphenyl)-3-(S)-iso-propyl-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ja/reaction/971371

反応式

関与物質

役割名称HCID仕込み量
反応物Tri-o-tolylphosphineHCID 80271—
反応物1-Benzyl-3-bromobenzeneHCID 597532—
反応物Sodium t-butoxideHCID 23676156—
反応物(S)-1-Boc-3-isopropylpiperazineHCID 24820348—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
溶媒Dichloromethane methanolHCID 21226129—
生成物4-(3'-Benzylphenyl)-3-(S)-iso-propyl-piperazine-1-carboxylic acid tert-butyl esterHCID 6912986922.71%

反応条件

温度100 °C

反応手順

17.9 mg (19.55 μmol, 0.044 eq.) Pd2(dba)3 and 5.9 mg (19.38 μmol, 0.044 eq.) P(o-tolyl)3 were dissolved in 6 ml dry toluene. Then 58.9 mg (610 μmol, 1.39 eq.) NaOt-Bu was added, followed by a solution of 101 mg (442 μmol) 3-(S)-Isopropyl-piperazine-1-carboxylic acid tert-butyl ester (85) and 110 mg (445 μmol, 1.01 eq.) 1-Benzyl-3-bromo-benzene (87). The resulting mixture was heated at 100° C. for 19 h. After filtrating the reaction mixture through celite the solvent was evaporated. Column chromatography (hexanes/EtOAc (3+1)) yielded 39.6 mg (100 μmol, 22.71%) 4-(3′-Benzylphenyl)-3-(S)-iso-propyl-piperazine-1-carboxylic acid tert-butyl ester (88).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07312246B2
出典データセットuspto-grants-2007_12
ORD IDord-b3aa74f75dd149ac9eceba8865b55e14
出典メモuspto-grants-2007_12