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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13417생성일: 2026년 10월 25일

2-Mercaptoethanol → 2-(5-((6-(1-Acetylpyrrolidin-2-yl)-2-pyridin-2-yl-1H-benzimidazol-5-yl)oxy)pyridin-2-ylsulfanyl)ethanol

https://huagongshe.com/reaction/13417

반응식

참여 물질

역할이름HCID투입량
반응물2-MercaptoethanolHCID 1567—
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물6-(1-Acetylpyrrolidin-2-yl)-5-((6-chloropyridin-3-yl)oxy)-2-pyridin-2-yl-1H-benzimidazoleHCID 23145102—
용매Sodium BicarbonateHCID 516892—
생성물2-(5-((6-(1-Acetylpyrrolidin-2-yl)-2-pyridin-2-yl-1H-benzimidazol-5-yl)oxy)pyridin-2-ylsulfanyl)ethanolHCID 23145115—

반응 조건

온도120 °C

반응 단계

20 mg of 2-mercaptoethanol and 10 mg of potassium carbonate were added in order to an N,N-dimethylformamide (1 ml) solution of 20 mg of 6-(1-acetylpyrrolidin-2-yl)-5-(6-chloropyridin-3-yl)oxy-2-pyridin-2-yl-1H-benzimidazole obtained in Example 504, and the reaction liquid was stirred at 120° C. for 5 hours. After cooled, the reaction liquid was diluted with aqueous saturated sodium bicarbonate, extracted with chloroform, and the organic layer was dried with anhydrous magnesium sulfate, and the solvent was evaporated away under reduced pressure. The resulting residue was purified through partitioning thin-layer chromatography (Kieselgel™ 60F254, Art 5744 (by Merck), chloroform/methanol=10/1) to obtain the entitled compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728025B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-789f003969094e3887548f5c03ce85d9
출처 메모uspto-grants-2010_06