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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 519620생성일: 2026년 10월 24일

Toluene → HCID 178438717, 화합물

https://huagongshe.com/ko/reaction/519620

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물3-Ethoxy-2-methyl-3-oxopropane-1-diazoniumHCID 86644035—
반응물HCID 178438707HCID 178438707—
촉매HCID 178476747HCID 178476747—
생성물HCID 178438717HCID 17843871750%

반응 단계

To a mixture of 3′-fluoro-4′-{[4-(trans-4-hydroxycyclohexyl)-2-methyl-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrile (0.46 g), rhodium(I) acetate (0.004 g) and toluene (10 mL) was added dropwise 3-ethoxy-2-methyl-3-oxopropane-1-diazonium (0.69 mL) at 80° C., and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was concentrated, and the obtained residue was purified by silica gel column chromatography. The obtained residue was dissolved in tetrahydrofuran (10 mL), and methylmagnesium bromide (1.0 M tetrahydrofuran solution, 2.5 mL) was added at room temperature. The reaction mixture was stirred for 1 hr, 1 N hydrochloric acid was added, and the mixture was extracted with ethyl acetate. The obtained ethyl acetate layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.27 g, 50%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115136B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-031f0813daa34434ac08a47965aae66e
출처 메모uspto-grants-2015_08