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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(4-chloro-2-ethylsulfanylphenyl)-7-trifluoromethyl-3H-quinazolin-4-one | HCID 136968750 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Chloro-2-(4-chloro-2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline | HCID 118035576 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260436B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-864f45592ede4c7eb31ad656954b67a0 |
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| Source note | uspto-grants-2016_02 |
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