Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diketene | HCID 12661 | — |
| Edukt | 4-Chloro-M-phenylenediamine | HCID 21209 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 4-Methyl-6-chloro-7-aminoquinolone | HCID 11195145 | 92% |
Reaktionsschritte
28.6 g of 4-chloro-1,3-phenylendiamine are suspended at 22° C. in 400 ml of toluene. 17.6 g of diketene in 100 ml of toluene are added to the grey suspension in the course of 30 minutes at 25±2° C., the suspension briefly passing into solution before the mono-diketenisation product is precipitated in the form of a beige solid. Stirring is then carried out for 6 h at 22° C. Then 5 g of pyridinium para-toluenesulfonate (PPTS) are added and the mixture is boiled under reflux for 16 h. The yellow suspension is cooled to 30° C., with stirring, and then at 30° C. 30 ml of 1 N NaOH are added. A further 100 ml of water are then added. The crude product is filtered at 22° C., washed neutral with H2O and dried overnight at 60° C. in vacuo. 38.5 g (yield: 92%, isomeric ratio of 4-methyl-6-chloro-7-aminoquinolone to 4-methyl-5-amino-6-chloroquinolone>95:5) of a beige solid having a melting point of 350° C. are obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07144993B2 |
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| Quelldatensatz | uspto-grants-2006_12 |
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| ORD ID | ord-5272b2e9b7384f5c9b0cedefa6e3f25a |
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| Quellennotiz | uspto-grants-2006_12 |
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