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HRID 130397作成日:2026年10月24日

Cesium carbonate → cis-3,5-Dimethyl-1-[2-(methyloxy)-5-nitrophenyl]piperazine

https://huagongshe.com/ja/reaction/130397

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物2-Bromo-4-nitroanisoleHCID 78870—
反応物Binap, (A+-)-HCID 634876—
反応物rel-(2R,6S)-2,6-dimethylpiperazineHCID 6950261—
触媒palladium(II) acetateHCID 167845—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物cis-3,5-Dimethyl-1-[2-(methyloxy)-5-nitrophenyl]piperazineHCID 59007077—

反応手順

Cesium carbonate (9.77 g, 30 mmol), palladium (II) acetate (448 mg, 2 mmol) and rac-2,2′-bis(diphenylphosphino)-1,1′-binapthyl (1.87 g, 3 mmol) were stirred under an inert atmosphere in tetrahydrofuran (40 ml) for 30 minutes. 2-Bromo-4-nitroanisole (4.64 g, 20 mmol) and cis-2,6-dimethylpiperazine (6.85 g, 60 mmol) in tetrahydrofuran (20 ml) was added and the mixture heated at reflux for 24 hours. After cooling to room temperature the reaction mixture was diluted with ethyl acetate and extracted with 2N hydrochloric acid (×3). The aqueous extract was stirred with ethyl acetate and activated charcoal, filtered through celite. The aqueous component of the filtrate was separated and the pH of the solution was adjusted to pH 7 with 50% potassium hydroxide solution and the solution evaporated in vacuo to a small volume. The residue was basified to pH 10 with 50% potassium hydroxide solution and extracted with dichloromethane (×3). The combined organic extracts were washed with saturated brine, dried over anhydrous sodium sulfate and concentrated in vacuo to afford the title product (D1). MS (ES+) m/e 266 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07381728B2
出典データセットuspto-grants-2008_06
ORD IDord-6d92d0e683b643f7adf8a5f3a68a5fca
出典メモuspto-grants-2008_06