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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517269Generated: October 27, 2026

Triethyl Phosphate → 4-(2,5-Dioxo-1-(3-(trifluoromethyl)phenyl)-1,2,3,4,5,6,7,8-octahydroquinazolin-4-yl)-3-(ethylsulfonyl)benzonitrile

https://huagongshe.com/reaction/517269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl PhosphateHCID 6535—
Reactant1,3-CyclohexanedioneHCID 10434—
ReactantPhosphorus oxide (P4O10)HCID 14812—
Reactant(3-Trifluoromethylphenyl)ureaHCID 25712—
Reactant3-(Ethylsulfonyl)-4-formylbenzonitrileHCID 58133833—
Solventtert-Butyl methyl etherHCID 15413—
Product4-(2,5-Dioxo-1-(3-(trifluoromethyl)phenyl)-1,2,3,4,5,6,7,8-octahydroquinazolin-4-yl)-3-(ethylsulfonyl)benzonitrileHCID 86732394—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of triethyl phosphate (4.6 mL, 26.9 mmol) and phosphorous pentoxide (2.54 g, 17.9 mmol) is heated at 50° C. over night and dilutet with tert-butyl methyl ether (45 mL). Cyclohexane-1,3-dione (3.77 g, 33.6 mmol), 3-(ethylsulfonyl)-4-formylbenzonitrile (5.00 g, 22.4 mmol) and 1-(3-(trifluoromethyl)phenyl)urea (4.57 g, 22.4 mmol) are added, and the mixture is heated at reflux for 4 h. The mixture is cooled at room temperature and concentrated under reduced pressure. The residue is purified by reversed phase HPLC (Agilent ZORBAX™ SB-C18, gradient of acetonitrile in water, 0.15% formic acid). Yield: 930 mg; ESI mass spectrum [M+H]+=504; Retention time HPLC: 1.02 min (Z017_S04).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115093B2
Source datasetuspto-grants-2015_08
ORD IDord-b748e31193424503b6b1460c49870459
Source noteuspto-grants-2015_08