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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37862생성일: 2026년 10월 25일

Cesium carbonate → 1-(4,6-Dimethyl-pyridin-2-yl)-4-(2-methyl-4-nitro-phenyl)-piperazine

https://huagongshe.com/reaction/37862

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물Benzene, 1-chloro-2-methyl-4-nitro-HCID 83315—
반응물1-(4,6-Dimethylpyridin-2-YL)piperazineHCID 23368063—
촉매palladium(II) acetateHCID 167845—
용매TolueneHCID 1140—
생성물1-(4,6-Dimethyl-pyridin-2-yl)-4-(2-methyl-4-nitro-phenyl)-piperazineHCID 6685152427.1%

반응 단계

Caesium carbonate (10.19 g, 31.38 mmol), 1-chloro-2-methyl-4-nitro-benzene (0.98 g, 5.75 mmol) and 1-(4,6-dimethyl-pyridin-2-yl)-piperazine (1.0 g, 5.23 mmol) were taken in toluene (35 mL) and degassed with argon for 15 min. A slurry of 2-dicyclophosphino-2′-(N,N-dimethylamino)-biphenyl (0.2 g, 0.52 mmol) and palladium acetate (0.116 g, 0.52 mmol) in toluene (5 mL) was added, the mixture degassed for another 10 min and then heated at reflux for 16 h. The mixture was cooled to room temperature and filtered, washing with ethyl acetate. The filtrate was washed with 2N hydrochloric acid, water, and brine, dried over anhydrous sodium sulfate, filtered and concentrated under vacuum to obtain the crude compound. Purification by column chromatography over silica gel (100-200 mesh) using 0-12% ethyl acetate in petroleum ether as eluent gave 1-(4,6-dimethyl-pyridin-2-yl)-4-(2-methyl-4-nitro-phenyl)-piperazine (0.463 g, 27%) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524705B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-1dcc0993a9df45538c543723262d88fe
출처 메모uspto-grants-2013_09