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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1688451생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1688451

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물3-BromocyclohexeneHCID 137057—
반응물4'-[(2-Methyl-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)methyl]biphenyl-2-carbonitrileHCID 136041272—
용매Ethyl AcetateHCID 8857—
생성물4'-{[4-(Cyclohex-2-en-1-yl)-2-methyl-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrileHCID 6700922117%

반응 단계

A mixture of 4′-[(2-methyl-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)methyl]biphenyl-2-carbonitrile (5 g), sodium hydride (0.62 g) and N,N-dimethylformamide (50 mL) was stirred at room temperature for 10 min, 3-bromocyclohexene (1.8 mL) was added, and the mixture was stirred at the same 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 (1 g, 17%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08148383B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-8d1f6b7b2af74d2eb3bab46e168e1582
출처 메모uspto-grants-2012_04