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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2062399생성일: 2026년 10월 26일

Dimethylformamide → 4'-{[4-(Methoxymethyl)-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}-3'-fluorobiphenyl-2-carbonitrile

https://huagongshe.com/reaction/2062399

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참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Chloromethyl Methyl EtherHCID 7864—
반응물Potassium CarbonateHCID 11430—
반응물3'-Fluoro-4'-[(5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)methyl]biphenyl-2-carbonitrileHCID 136337139—
용매Ethyl AcetateHCID 8857—
생성물4'-{[4-(Methoxymethyl)-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}-3'-fluorobiphenyl-2-carbonitrileHCID 6700950569%

반응 단계

A mixture of 3′-fluoro-4′-[(5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)methyl]biphenyl-2-carbonitrile (0.5 g), chloro(methoxy)methane (0.12 mL), potassium carbonate (0.36 g) and N,N-dimethylformamide (10 mL) was stirred at room temperature for 1 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 (0.38 g, 69%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08283353B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-29c0ecdc406d4b13b1bb909e0f70181c
출처 메모uspto-grants-2012_10