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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734650Generated: October 25, 2026

1-Fluoro-3-isocyanato-5-(trifluoromethyl)benzene → 2-acetylamino-4-{4-[3-(3-fluoro-5-trifluoromethylphenyl)ureido]phenyl}-1H-pyrrole-3-carboxamide

https://huagongshe.com/reaction/734650

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Fluoro-3-isocyanato-5-(trifluoromethyl)benzeneHCID 3445672—
Reactant2-acetylamino-4-(4-aminophenyl)-1H-pyrrole-3-carboxamideHCID 69061860—
SolventTetrahydrofuranHCID 8028—
Product2-acetylamino-4-{4-[3-(3-fluoro-5-trifluoromethylphenyl)ureido]phenyl}-1H-pyrrole-3-carboxamideHCID 5784555141.8%

Reaction Steps

0.061 cm3 (0.426 mmol) of 3-fluoro-5-trifluoromethylphenyl isocyanate is added at room temperature to a suspension of 100 mg (0.387 mmol) of 2-acetylamino-4-(4-aminophenyl)-1H-pyrrole-3-carboxamide in 5 cm3 of anhydrous tetrahydrofuran. The reaction medium is stirred at room temperature for 24 hours, cooled in a water-ice bath and then filtered on sintered glass. The solid collected is washed with a small amount of dichloromethane and cyclohexane and then dried under vacuum. 75 mg of 2-acetylamino-4-{4-[3-(3-fluoro-5-trifluoromethylphenyl)ureido]phenyl}-1H-pyrrole-3-carboxamide are obtained in the form of a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592365B2
Source datasetuspto-grants-2009_09
ORD IDord-4cd57cb910dd432b8625224f499fdc1c
Source noteuspto-grants-2009_09