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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241527Generated: October 30, 2026

Acetic Acid → 1-[(E)-[4-[3-(3,5-dichlorophenyl)-3-(trifluoromethyl)-2,4-dihydropyrrol-5-yl]-2-methylphenyl]methylideneamino]-3-(2,2,2-trifluoroethyl)urea

https://huagongshe.com/reaction/241527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
Reactant1-Amino-3-(2,2,2-trifluoroethyl)ureaHCID 43163995—
Reactant4-[3-(3,5-Dichlorophenyl)-3-(trifluoromethyl)-2,4-dihydropyrrol-5-yl]-2-methyl-benzaldehydeHCID 86691047—
SolventEthanolHCID 702—
Product1-[(E)-[4-[3-(3,5-dichlorophenyl)-3-(trifluoromethyl)-2,4-dihydropyrrol-5-yl]-2-methylphenyl]methylideneamino]-3-(2,2,2-trifluoroethyl)ureaHCID 5696123473%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 4-[3-(3,5-dichlorophenyl)-3-(trifluoromethyl)-2,4-dihydropyrrol-5-yl]-2-methyl-benzaldehyde (i.e. the product of Step 5, 200 mg), 1-amino-3-(2,2,2-trifluoroethyl)urea (145 mg) and acetic acid (0.1 mL) in EtOH (5 mL) was heated at 70° C. for 4 h. Water was added, the reaction cooled to room temperature and the solid was collected by filtration. Recrystallization from diisopropylether yielded the title compound (198 mg, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653000B2
Source datasetuspto-grants-2014_02
ORD IDord-b72aeca1527e4bd9b29b6660eab933cd
Source noteuspto-grants-2014_02