HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Potassium Hydroxide → 6-Bromo-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Propiophenone, 3'-(trifluoromethyl) | HCID 137064 | — |
| Edukt | 5-bromo-6-methoxy-1H-indole-2,3-dione | HCID 14595061 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 6-Bromo-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid | HCID 67383828 | 44,2% |
Reaktionsschritte
A solution of 5-bromo-6-(methyloxy)-1H-indole-2,3-dione (75 g, 293 mmol), KOH (98.5 g, 1760 mmol) in EtOH (500 mL) and H2O (150 mL) was stirred followed by the addition of 1-[3-(trifluoromethyl)phenyl]-1-propanone (59 g, 293 mmol) in one portion. After refluxing for 16 h, the mixture was evaporated to remove EtOH and pH adjusted to 3 with 2N HCl. Following filtration to yield the crude product, the material was refluxed in EtOH (1 L) for 1 h, filtered and dried to yield 6-bromo-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid (57 g, 44% yield) as an off white solid. MS (m/z) 440 (M+H+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08658636B2 |
| Quelldatensatz | uspto-grants-2014_02 |
| ORD ID | ord-0efd84bacb604f3486499c2a8def17b4 |
| Quellennotiz | uspto-grants-2014_02 |