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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1509516생성일: 2026년 10월 26일

2-Chloroethyl vinyl ether → tert-butyl(3S,5R)-3-[({1-[2-(ethenyloxy)ethyl]-1H-benzimidazol-2-yl}carbonyl)(2-methylpropyl)amino]-5-(morpholin-4-ylcarbonyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1509516

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참여 물질

역할이름HCID투입량
반응물2-Chloroethyl vinyl etherHCID 8074—
반응물Cesium carbonateHCID 10796—
반응물tert-Butyl (3S,5R)-3-{(1H-benzimidazol-2-ylcarbonyl)(2-methylpropyl)amino)-5-(morpholin-4-ylcarbonyl)piperidine-1-carboxylateHCID 58355717—
촉매Potassium IodideHCID 4875—
용매WaterHCID 962—
용매DimethylacetamideHCID 31374—
생성물tert-butyl(3S,5R)-3-[({1-[2-(ethenyloxy)ethyl]-1H-benzimidazol-2-yl}carbonyl)(2-methylpropyl)amino]-5-(morpholin-4-ylcarbonyl)piperidine-1-carboxylateHCID 5835522892.3%

반응 조건

온도60 °C

반응 단계

To a solution of tert-butyl (3S,5R)-3-{(1H-benzimidazol-2-ylcarbonyl)(2-methylpropyl)amino}-5-(morpholin-4-ylcarbonyl)piperidine-1-carboxylate (308 mg), (2-chloroethoxy)ethene (192 mg) and potassium iodide (5 mg) in N,N-dimethylacetamide (5 ml) was added cesium carbonate (586 mg), and the mixture was stirred at 60° C. for 15 hr. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, and a fraction eluted with ethyl acetate-hexane (6:4) was concentrated under reduced pressure to give the object product (323 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09221836B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-1ebcf4d71fc24df1aa6267823a0da6e6
출처 메모uspto-grants-2015_12