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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927193Generated: November 2, 2026

Water → 4-(4-Bromophenyl)-1-(3-(difluoromethyl)phenyl)-3,4,6,7-tetrahydro-1H-cyclopenta[d]-pyrimidine-2,5-dione

https://huagongshe.com/reaction/927193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Bromo-4-(chloro(isocyanato)methyl)benzeneHCID 11687418—
Reactant3-(3-(Difluoromethyl)phenylamino)cyclopent-2-enoneHCID 90310964—
SolventDichloromethaneHCID 6344—
Product4-(4-Bromophenyl)-1-(3-(difluoromethyl)phenyl)-3,4,6,7-tetrahydro-1H-cyclopenta[d]-pyrimidine-2,5-dioneHCID 90311061—

Reaction Steps

A solution of 1-bromo-4-(chloro(isocyanato)methyl)benzene (240 mg, 0.974 mmol) in dichloromethane (2 mL) is added dropwise to a solution of 3-(3-(difluoromethyl)phenyl-amino)cyclopent-2-enone (intermediate 5, 217 mg, 0.974 mmol) in dichloromethane (2 mL) and the reaction mixture is heated at reflux for 2 h. Water is added, and the phases are extracted twice with dichloromethane. The combined organic layers are concentrated and the residue is purified by flash chromatography on silica (gradient cyclohexane/ethyl acetate 4:1 to ethyl acetate). Yield: 159 mg; ESI mass spectrum: [(79Br)-M+H]+=433, [(81Br)-M+H]+=435; Retention time HPLC: 0.56 min (X012_S01).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290459B1
Source datasetuspto-grants-2016_03
ORD IDord-f87c092bff3b4f0e9819029150100ea2
Source noteuspto-grants-2016_03