Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbamic acid, ethyl ester | HCID 5641 | — |
| Reactant | 2-(2,2,2-Trifluoroethylamino)-5-chlorobenzophenone | HCID 89821 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Fluquazone | HCID 219069 | 73.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04202895 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-2104eabaa0df4b47b01079133fcb8174 |
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| Source note | uspto-grants-1980_05 |
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