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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 270857생성일: 2026년 10월 26일

Dimethylformamide → 2-(3-Amino-4-bromo-5-phenyl-pyrazol-1-yl)-1-[4-(4-fluoro-phenyl)-piperazin-1-yl]-ethanone

https://huagongshe.com/reaction/270857

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물4-Bromo-3-phenyl-1H-pyrazol-5-amineHCID 594319—
반응물1-(Chloroacetyl)-4-(4-fluorophenyl)piperazineHCID 1848511—
용매Ethyl acetate hexaneHCID 21226206—
생성물2-(3-Amino-4-bromo-5-phenyl-pyrazol-1-yl)-1-[4-(4-fluoro-phenyl)-piperazin-1-yl]-ethanoneHCID 21071045—

반응 단계

Protocol T was followed using 4-Bromo-5-phenyl-1H-pyrazol-3-ylamine, K2CO3, 2-Chloro-1-[4-(4-fluoro-phenyl)-piperazin-1-yl]-ethanone and DMF. Column chromatography using a solvent mixture (hexane/ethyl acetate=3/7) afforded the title compound as yellow solid. 1H NMR (400 MHz, CDCl3): 7.74-7.78 (m, 2H), 7.24-7.36 (m, 3H), 6.86-6.92 (m, 2H), 6.74-6.78 (m, 2H), 4.9 (s, 2H), 4.22 (s, 2H), 3.64-3.74 (m, 4H), 2.86-3.04 (m, 4H). 13C NMR (400 MHz, CDCl3): 164, 146.2, 144.8, 128, 126.8, 118, 114.8, 60, 50.2, 50, 48.8, 46, 42, 20.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449576B1
출처 데이터셋uspto-grants-2008_11
ORD IDord-9022d53f02c74592a232491dfdcb1553
출처 메모uspto-grants-2008_11