HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Piperidine → 6,7-Difluoroquinazolin-4(3H)-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Piperidine | HCID 8082 | — |
| Edukt | 1,3,5-Triazine | HCID 9262 | — |
| Edukt | 2-Amino-4,5-difluorobenzoic acid | HCID 735965 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 6,7-Difluoroquinazolin-4(3H)-one | HCID 135471308 | 86% |
Reaktionsschritte
To a solution of 4.81 g (27.8 mmol) of commercially available 2-amino-4,5-difluorobenzoic acid in 20 ml of ethanol were added 1.92 ml (19.4 mmol) of piperidine and 2.25 g (27.8 mmol) of 1,3,5-triazine, followed by heating under reflux in an atmosphere of argon for 6.5 hours. After the reaction mixture was allowed to cool to room temperature, the solvent was evaporated. To the residue was added water, and the resulting mixture was neutralized with 4 N hydrochloric acid. The precipitated crystals were collected by filtration, washed with water, and dried to give 4.37 g (86%) of 6,7-difluoro-4(3H)-quinazolone.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06750218B2 |
| Quelldatensatz | uspto-grants-2004_06 |
| ORD ID | ord-26367b7bf5f44bffb86b8d2214bf5dda |
| Quellennotiz | uspto-grants-2004_06 |