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HRID 1919692생성일: 2026년 10월 26일

Potassium Carbonate → 1-(3-Chloro-4-nitrophenyl)-4-methylpiperazine

https://huagongshe.com/reaction/1919692

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1-MethylpiperazineHCID 53167—
반응물2-Chloro-4-fluoro-1-nitrobenzeneHCID 75017—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물1-(3-Chloro-4-nitrophenyl)-4-methylpiperazineHCID 23139607—

반응 단계

2-chloro-4-fluoronitrobenzene (1.0 eq, 1 g, 5.7 mmol), N-methyl piperazine (1.2 eq, 1.18 g, 6.84 mmol), potassium carbonate (2.0 eq, 1.6 g, 11.6 mmol) were stirred at 100° C. in DMF for 3 hours. The mixture was cooled down and diluted with water. The material was extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4 and the solvent evaporated in vacuo. After trituration in diethylether and filtration, 1-(3-chloro-4-nitrophenyl)-4-methylpiperazine was isolated as a solid (0.9 g, 62%). LCMS (ES): m/z 256 [M+1]+. This material was suspended in MeOH (20 ml) with Raney Nickel (0.2 g) and stirred under hydrogen atmosphere overnight. The catalyst was filtered off through celite. Evaporation of the solvents provided 2-chloro-4-(4-methylpiperazin-1-yl)aniline as a dark brown oil (0.68 g, 86%). LCMS (ES): m/z 226 [M+1]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08168651B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-147d905ba43d462ba6ab47f10fe2c133
출처 메모uspto-grants-2012_05