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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45839생성일: 2026년 10월 24일

Water → 1-(3-{4-[2-(tert-butylamino)pyridin-4-yl]-1-(4-methoxybenzyl)-1H-pyrazol-3-yl}phenyl)-3-[4-(trifluoromethyl)phenyl]urea

https://huagongshe.com/ko/reaction/45839

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4-(Trifluoromethyl)phenyl isocyanateHCID 73768—
반응물4-[3-(3-aminophenyl)-1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-N-tert-butyl-pyridin-2-amineHCID 67184018—
용매DimethylformamideHCID 6228—
생성물1-(3-{4-[2-(tert-butylamino)pyridin-4-yl]-1-(4-methoxybenzyl)-1H-pyrazol-3-yl}phenyl)-3-[4-(trifluoromethyl)phenyl]ureaHCID 6718478570%

반응 단계

40 mg (0,094 mmol) of 4-[3-(3-aminophenyl)-1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-N-tert-butylpyridin-2-amine were dissolved in 2 ml of dry dimethylformamide and 12 μL (0.094 mmol) of p-trifluoromethylphenylisocyanate were added. The solution was stirred at room temperature for 3 hours. The reaction mixture was then poured into water and the product extracted several times with ethylacetate. The organic layer was dried over Na2SO4 and evaporated to dryness. The crude was purified by chromatography on a silica gel column eluted with dichloromethane-acetone 9/1, affording 40 mg (70% yield) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541575B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-61f7e482f0854b58baf8909c96362d73
출처 메모uspto-grants-2013_09