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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130397생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2-Bromo-4-nitroanisoleHCID 78870—
반응물Binap, (A+-)-HCID 634876—
반응물rel-(2R,6S)-2,6-dimethylpiperazineHCID 6950261—
촉매palladium(II) acetateHCID 167845—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물cis-3,5-Dimethyl-1-[2-(methyloxy)-5-nitrophenyl]piperazineHCID 59007077—

반응 단계

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]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381728B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-6d92d0e683b643f7adf8a5f3a68a5fca
출처 메모uspto-grants-2008_06