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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13329생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/13329

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물5-Bromopyrimidine-2-carbonitrileHCID 686546—
반응물5-(2-fluorophenoxy)-6-hydroxy-2-pyrazin-2-yl-1H-benzimidazoleHCID 135697984—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물5-(2-Fluoro-phenoxy)-2-pyrazin-2-yl-6-(6-cyano-pyridin-3-yloxy)-1H-benzimidazoleHCID 23145142—

반응 조건

온도90 °C

반응 단계

7.0 mg of 5-bromo-2-cyano-pyrimidine and 15 mg of cesium carbonate were added to an N-methylpyrrolidinone (0.5 ml) solution of 7.0 mg of 5-(2-fluorophenoxy)-6-hydroxy-2-pyrazin-2-yl-1H-benzimidazole obtained in the step 1, and the reaction liquid was stirred at 90° C. for 15 minutes. The reaction mixture 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 a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728025B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-16448ad5041148a9ab574d8ff2b42526
출처 메모uspto-grants-2010_06