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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 270856생성일: 2026년 10월 26일

Dimethylformamide → 2-{2-[4-(4-Fluoro-phenyl)-piperazin-1-yl]-2-oxo-ethyl}-5-thiophen-2-yl-2H-pyrazole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/270856

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물1-(Chloroacetyl)-4-(4-fluorophenyl)piperazineHCID 1848511—
반응물HCID 178468642HCID 178468642—
용매Ethyl acetate hexaneHCID 21226206—
생성물2-{2-[4-(4-Fluoro-phenyl)-piperazin-1-yl]-2-oxo-ethyl}-5-thiophen-2-yl-2H-pyrazole-3-carboxylic acid ethyl esterHCID 58778027—

반응 단계

Protocol T was followed using 5-Thiophen-2-yl-2H-pyrazole-3-carboxylic acid ethyl ester, K2CO3, 2-Chloro-1-[4-(4-fluoro-phenyl)-piperazin-1-yl]-ethanone and DMF. Column chromatography using a solvent mixture (hexane/ethyl acetate=1.5/1) afforded the title compound. 1H NMR (400 MHz, CDCl3): 7.32-7.36 (m, 1H), 7.22-7.26 (m, 1H), 7.08 (s, 1H), 7.02-7.08 (dd, 1H), 6.96-7.2 (m, 2H), 6.86-6.92 (m, 2H), 4.3-4.4 (q, 2H), 3.52-3.58 (m, 4H), 3.05-3.25 (m, 4H), 1.3-1.42 (m, 3H). 13C NMR (400 MHz, CDCl3): 164, 130, 126.8, 126.4, 120, 118.2, 115.4, 62.3, 54, 50.5, 42, 44.5, 14.6.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449576B1
출처 데이터셋uspto-grants-2008_11
ORD IDord-37a3768cf95548788e225162bc3a5641
출처 메모uspto-grants-2008_11