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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1403142생성일: 2026년 10월 26일

Ethanol → 1-{4-[({4-[2-(difluoromethyl)-1H-benzimidazol-1-yl]-6-(morpholin-4-yl)pyrimidin-2-yl}amino)methyl]piperidin-1-yl}-3-fluoropropan-2-ol

https://huagongshe.com/reaction/1403142

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물1,2-Epoxy-3-fluoropropaneHCID 10418—
반응물DiisopropylethylamineHCID 81531—
반응물4-[2-(difluoromethyl)-1H-benzimidazol-1-yl]-6-morpholin-4-yl-N-(piperidin-4-ylmethyl)pyrimidin-2-amineHCID 86686777—
용매WaterHCID 962—
생성물1-{4-[({4-[2-(difluoromethyl)-1H-benzimidazol-1-yl]-6-(morpholin-4-yl)pyrimidin-2-yl}amino)methyl]piperidin-1-yl}-3-fluoropropan-2-olHCID 86686776—

반응 조건

온도120 °C

반응 단계

To a mixture of 4-[2-(difluoromethyl)-1H-benzimidazol-1-yl]-6-morpholin-4-yl-N-(piperidin-4-ylmethyl)pyrimidin-2-amine (100 mg) and ethanol (2 mL) were added 2-(fluoromethyl)oxirane (19 μL) and N,N-diisopropyl ethylamine (79 μL), and the mixture was stirred in a microwave reactor at 120° C. for 1 hour. To the reaction mixture was added water, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and then the residue was purified by amino silica gel column chromatography (ethyl acetate:hexane) to obtain 1-{4-[({4-[2-(difluoromethyl)-1H-benzimidazol-1-yl]-6-(morpholin-4-yl)pyrimidin-2-yl}amino)methyl]piperidin-1-yl}-3-fluoropropan-2-ol (81 mg) as a white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08912180B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-38e3e188e5524b7691b98d0105a36a12
출처 메모uspto-grants-2014_12