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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1810963생성일: 2026년 10월 27일

1-(2-Nitrophenyl)piperazine → 2-(3,5-Dimethyl-pyrazol-1-yl)-1-[4-(2-nitro-phenyl)-piperazin-1-yl]-ethanone

https://huagongshe.com/reaction/1810963

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-Nitrophenyl)piperazineHCID 100949—
반응물(3,5-Dimethyl-1H-pyrazol-1-yl)acetic acidHCID 572875—
반응물Bis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-(3,5-Dimethyl-pyrazol-1-yl)-1-[4-(2-nitro-phenyl)-piperazin-1-yl]-ethanoneHCID 2700799164%

반응 단계

To (3,5-dimethyl-pyrazol-1-yl)-acetic acid (0.140 g, 0.908 mmol) in DMF is added carbonyl diimidazole (0.140 g, 0.863 mmol) in one portion. The mixture is stirred for 1 h. To this is added 1-(2-nitro-phenyl)-piperazine (0.197 g, 0.950 mmol). The mixture is stirred for 14 h and then diluted with 100 mL EtOAc. The reaction is quenched with 20 mL of saturated NH4Cl, washed with 2×20 mL of H2O and 1×20 mL of brine. The organic phase is dried (MgSO4), filtered and concentrated to give 2-(3,5-dimethyl-pyrazol-1-yl)-1-[4-(2-nitro-phenyl)-piperazin-1-yl]-ethanone in 64% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08362249B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-d5cbc1d651ec4ba2922786484632b56e
출처 메모uspto-grants-2013_01