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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45859Generated: October 25, 2026

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/reaction/45859

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)phenyl isocyanateHCID 73768—
ReactantSodiumHCID 5360545—
Reactant4-[3-(3-aminophenyl)-1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-N-tert-butyl-pyridin-2-amineHCID 67184018—
SolventDimethylformamideHCID 6228—
Product1-(3-{4-[2-(tert-butylamino)pyridin-4-yl]-1-(4-methoxybenzyl)-1H-pyrazol-3-yl}phenyl)-3-[4-(trifluoromethyl)phenyl]ureaHCID 6718478560%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541575B2
Source datasetuspto-grants-2013_09
ORD IDord-1e25fcda39bd496e89515e1abb5c512d
Source noteuspto-grants-2013_09