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HRID 270858생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/270858

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물4-Bromo-3-phenyl-1H-pyrazol-5-amineHCID 594319—
반응물1-(Chloroacetyl)-4-(4-chlorophenyl)piperazineHCID 4053957—
용매Ethyl acetate hexaneHCID 21226206—
생성물2-(3-Amino-4-bromo-5-phenyl-pyrazol-1-yl)-1-[4-(4-chloro-phenyl)-piperazin-1-yl]-ethanoneHCID 21071044—

반응 단계

Protocol T was followed using 4-Bromo-5-phenyl-1H-pyrazol-3-ylamine, K2CO3, 2-Chloro-1-[4-(4-chloro-phenyl)-piperazin-1-yl]-ethanone and DMF. Column chromatography using a solvent mixture (hexane/ethyl acetate=1/4) afforded the title compound as white solid. 1H NMR (400 MHz, CDCl3); 7.7-7.8 (m, 2H), 7.24-7.3 (m, 3H), 6.8-6.92 (m, 2H), 6.74-6.78 (m, 2H), 4.9 (s, 2H), 4.2 (s, 2H), 3.6-3.7 (m, 4H), 2.86-3.04 (m, 4H). 13C NMR (400 MHz, CDCl3): 164, 146, 145, 128, 127, 118, 114.8, 60.2, 50.4, 50, 48.8, 46, 42, 22.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449576B1
출처 데이터셋uspto-grants-2008_11
ORD IDord-3b52df543c5541868cc6bfc0ee2fafeb
출처 메모uspto-grants-2008_11