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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395147Generated: October 30, 2026

Carbamic acid, ethyl ester → Fluquazone

https://huagongshe.com/reaction/1395147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbamic acid, ethyl esterHCID 5641—
Reactant2-(2,2,2-Trifluoroethylamino)-5-chlorobenzophenoneHCID 89821—
CatalystZincchlorideHCID 3007855—
SolventChloroformHCID 6212—
ProductFluquazoneHCID 21906973.1%

Reaction Conditions

Temperature190 °C

Reaction Steps

A mixture of 62.7 g of 2-(2,2,2-trifluoroethylamino)-5-chlorobenzophenone, 107 g of ethyl carbamate and 10 g of zinc chloride was heated at 190° C. (oil bath temperature) for 3 hours. After cooling, the reaction mixture was dissolved in chloroform and the insoluble material was filtered off. The chloroform solution was washed successively with dilute hydrochloric acid and water, and dried over anhydrous sodium sulfate. Then the solvent was removed under reduced pressure and the residual solid was washed 3 times with 100 ml of isopropyl ether and dried to give 49.5 g of 1-(2,2,2-trifluoroethyl)-4-phenyl-6-chloro-2(1H)-quinazolinone as a pale gray powder. Recrystallization from ethanol gave pale yellow needles, m.p. 186.5°-187.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04202895
Source datasetuspto-grants-1980_05
ORD IDord-2104eabaa0df4b47b01079133fcb8174
Source noteuspto-grants-1980_05