HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 521667Erstellt: 25. Oktober 2026
2-Amino-4-(trifluoromethyl)benzamide → 2-(4-chloro-2-ethylsulfanylphenyl)-7-trifluoromethyl-3H-quinazolin-4-one
https://huagongshe.com/reaction/521667
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Amino-4-(trifluoromethyl)benzamide | HCID 69739 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Sodium Bisulfite | HCID 23665763 | — |
| Edukt | 4-Chloro-2-ethylsulfanylbenzaldehyde | HCID 114863540 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 2-(4-chloro-2-ethylsulfanylphenyl)-7-trifluoromethyl-3H-quinazolin-4-one | HCID 136968750 | 80,7% |
Reaktionsschritte
A mixture of 1.0 g of 2-amino-4-trifluromethylbenzamide, 944 mg of 4-chloro-2-ethylsulfanylbenzaldehyde, 765 mg of sodium bisulfite and 4 ml of DMA was stirred at 150° C. for 15 hours. A saturated aqueous sodium bicarbonate solution and water were added to the cooled reaction mixture, and the precipitated solid was filtered. The resulting solid was washed with water and n-hexane and then dried to obtain 1.46 g of 2-(4-chloro-2-ethylsulfanylphenyl)-7-trifluoromethyl-3H-quinazolin-4-one.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09328121B1 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-8f4b80ef8cfc4a818ce6750c2e33ca20 |
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| Quellennotiz | uspto-grants-2016_05 |
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