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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45859생성일: 2026년 10월 23일

4-(Trifluoromethyl)phenyl isocyanate → 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/45859

반응식

참여 물질

역할이름HCID투입량
반응물4-(Trifluoromethyl)phenyl isocyanateHCID 73768—
반응물SodiumHCID 5360545—
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 6718478560%

반응 단계

350 mg (0.82 mmol) of 4-[3-(3-aminophenyl)-1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-N-tert-butyl-pyridin-2-amine were dissolved in 30 ml of dry dimethylformamide and 110 μl (0.82 mmol) of p-trifluoromethyl-phenyl isocyanate were added to the resulting solution. The mixture was stirred overnight at room temperature, then poured into an aqueous solution of sodium hydrogenocarbonate and extracted with dichloromethane. The organic phase was dried over sodium sulphate and evaporated in vacuo. The residue was chromatographed on a silica gel column (dichloromethane-acetone 9/1), affording 302 mg (60%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541575B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-1e25fcda39bd496e89515e1abb5c512d
출처 메모uspto-grants-2013_09