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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13331생성일: 2026년 10월 23일

Cesium carbonate → 5-(2-Fluoro-phenoxy)-2-pyrazin-2-yl-6-(6-trifluoromethyl-pyridin-3-yloxy)-1H-benzimidazole

https://huagongshe.com/ko/reaction/13331

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물5-Bromo-2-(trifluoromethyl)pyridineHCID 2761197—
반응물5-(2-fluorophenoxy)-6-hydroxy-2-pyrazin-2-yl-1H-benzimidazoleHCID 135697984—
촉매Copper oxideHCID 14829—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물5-(2-Fluoro-phenoxy)-2-pyrazin-2-yl-6-(6-trifluoromethyl-pyridin-3-yloxy)-1H-benzimidazoleHCID 23145778—

반응 조건

온도130 °C

반응 단계

16 mg of 5-bromo-2-trifluoromethyl-pyridine, 50 mg of cesium carbonate and 10 mg of copper(II) oxide were added to an N-methylpyrrolidinone (1 ml) solution of 21 mg of 5-(2-fluorophenoxy)-6-hydroxy-2-pyrazin-2-yl-1H-benzimidazole obtained in Example 251 (step 1), and the reaction liquid was stirred at 130° C. for 5 hours. The deposit was separated through filtration, and the solution was purified through reversed-phase middle-pressure liquid chromatography [ODS-AS-360-CC (by YMC), mobile phase: water-acetonitrile-0.1% trifluoroacetic acid]. The resulting fraction was diluted with ethyl acetate, washed with aqueous saturated sodium bicarbonate, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure to obtain the entitled compound as a brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728025B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-a8cabb912c264e1fb37b38fd8adc589b
출처 메모uspto-grants-2010_06