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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927194Generated: November 2, 2026

3-[3-(Trifluoromethyl)anilino]cyclopent-2-en-1-one → 4-(4-bromo-2-(methylsulfonyl)phenyl)-1-(3-(trifluoromethyl)phenyl)-3,4,6,7-tetrahydro-1H-cyclopentapyrimidine-2,5-dione

https://huagongshe.com/reaction/927194

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[3-(Trifluoromethyl)anilino]cyclopent-2-en-1-oneHCID 90311057—
Reactant4-Bromo-1-(chloro(isocyanato)methyl)-2-(methylsulfonyl)benzeneHCID 90311088—
SolventDichloromethaneHCID 6344—
Product4-(4-bromo-2-(methylsulfonyl)phenyl)-1-(3-(trifluoromethyl)phenyl)-3,4,6,7-tetrahydro-1H-cyclopentapyrimidine-2,5-dioneHCID 90311004—

Reaction Steps

3-(3-(Trifluoromethyl)phenylamino)cyclopent-2-enone (234 mg, 0.97 mmol) is added to a solution of 4-bromo-1-(chloro(isocyanato)methyl)-2-(methylsulfonyl)benzene (Step 1, 945 mg, 2.91 mmol) in dichloromethane (10 mL). The mixture is heated at reflux over night and then concentrated under reduced pressure. The residue is purified by reversed phase HPLC (Agilent ZORBAX™ SB—C18, gradient of acetonitrile in water, 0.1% formic acid). Yield: 110 mg; ESI mass spectrum: ESI mass spectrum: [(79Br)-M+H]+=529, [(81Br)-M+H]+=531; Retention time HPLC: 1.21 min (Z017_S04).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290459B1
Source datasetuspto-grants-2016_03
ORD IDord-d1c1d80ae4bc45a7aa95938feeec1b47
Source noteuspto-grants-2016_03