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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1412178생성일: 2026년 10월 26일

Pyridine → 3'-Fluoro-4'-[(5-oxo-4-phenyl-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)methyl]biphenyl-2-carbonitrile

https://huagongshe.com/reaction/1412178

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물TriethylamineHCID 8471—
반응물Phenylboronic AcidHCID 66827—
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—
촉매Cupric acetateHCID 8895—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물3'-Fluoro-4'-[(5-oxo-4-phenyl-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)methyl]biphenyl-2-carbonitrileHCID 67010029102%

반응 단계

To a suspension (20 mL) 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), phenylboronic acid (0.31 g), triethylamine (0.5 mL), pyridine (1 mL) and molecular sieves 4A (1 g) in dichloromethane was added copper(II) acetate (0.47 g), and the mixture was stirred for 16 hr. The reaction mixture was diluted with ethyl acetate, insoluble material was filtered off through celite, and the filtrate was concentrated. The residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.61 g, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08921379B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-400d11d21ecf48c2a281713a97a3a5ec
출처 메모uspto-grants-2014_12