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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775267Generated: November 1, 2026

Phosphorus oxychloride → 4-Chloro-2-(4-chloro-2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline

https://huagongshe.com/reaction/1775267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(4-chloro-2-ethylsulfanylphenyl)-7-trifluoromethyl-3H-quinazolin-4-oneHCID 136968750—
SolventTolueneHCID 1140—
Product4-Chloro-2-(4-chloro-2-ethylsulfanylphenyl)-7-trifluoromethylquinazolineHCID 118035576—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 1.46 g of 2-(4-chloro-2-ethylsulfanylphenyl)-7-trifluoromethyl-3H-quinazolin-4-one, 0.39 ml of phosphorus oxychloride, 538 mg of N,N-diisopropylethylamine and 20 ml of toluene was stirred at 90° C. for 1 hour. A saturated aqueous sodium bicarbonate solution was added to the cooled reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure to obtain 1.31 g of 4-chloro-2-(4-chloro-2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline (Compound of Present Invention 14).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260436B2
Source datasetuspto-grants-2016_02
ORD IDord-864f45592ede4c7eb31ad656954b67a0
Source noteuspto-grants-2016_02