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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32728생성일: 2026년 10월 23일

Imidazole → 1-{3-Fluoro-4-[4-(5-imidazol-1-yl-2-morpholin-4-yl-benzoyl)-piperazin-1-yl]-phenyl}-ethanone

https://huagongshe.com/ko/reaction/32728

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물1,10-PhenanthrolineHCID 1318—
반응물Cesium carbonateHCID 10796—
반응물1-(4-(4-(5-Bromo-2-morpholinobenzoyl)piperazin-1-yl)-3-fluorophenyl)ethanoneHCID 44580513—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매1,4-DioxaneHCID 31275—
생성물1-{3-Fluoro-4-[4-(5-imidazol-1-yl-2-morpholin-4-yl-benzoyl)-piperazin-1-yl]-phenyl}-ethanoneHCID 5979369641.9%

반응 조건

온도120 °C

반응 단계

In a tube were added successively 1-{4-[4-(5-Bromo-2-morpholin-4-yl-benzoyl)-piperazin-1-yl]-3-fluoro-phenyl}-ethanone (example BJ, 0.05 g, 0.1 mmol), imidazole (8.4 mg, 0.12 mmol), cesium carbonate (70 mg, 0.21 mmol), CuI (4 mg, 0.02 mmol), 1,10-phenanthroline (7.3 mg, 0.04 mmol) and dioxane (0.2 ml). The mixture was heated under argon at 120° C. for 12 hours. The reaction mixture was cooled to room temperature and quenched with water/ethyl acetate. The aqueous layer was extracted twice with ethylacetate. The organic layers were combined, dried over Na2SO4, filtered and the solvent was removed in vacuo. The crude oil was chromatographed over silicagel: eluent: CH2Cl2/methanol: 0-5% to provide the title compound as a brown solid (20 mg, 40%), MS (m/e): 478.4 (M+H, 100%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427612B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-a4c32b96617f474fb32d70c7f6e317c6
출처 메모uspto-grants-2008_09