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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1412248생성일: 2026년 10월 25일

Dimethylformamide → 4'-{[7-Butyl-4-(4-methoxycyclohexyl)-5-oxo-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrile

https://huagongshe.com/reaction/1412248

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참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물4'-{[7-Butyl-4-(4-hydroxycyclohexyl)-5-oxo-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrileHCID 67009672—
용매Ethyl AcetateHCID 8857—
생성물4'-{[7-Butyl-4-(4-methoxycyclohexyl)-5-oxo-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrileHCID 6700955642%

반응 단계

To a mixture of 4′-{[7-butyl-4-(4-hydroxycyclohexyl)-5-oxo-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrile (0.37 g), methyl iodide (0.053 mL) and N,N-dimethylformamide (10 mL) was added sodium hydride (0.034 g), and the mixture was stirred at room temperature for 16 hr. The reaction mixture was diluted with ethyl acetate, washed with 5% aqueous potassium hydrogensulfate solution and then with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.16 g, 42%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08921379B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-7cba39abc02a494c810d3569512ba7f5
출처 메모uspto-grants-2014_12