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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 353159Erstellt: 24. Oktober 2026

Piperidine → 6,7-Difluoroquinazolin-4(3H)-one

https://huagongshe.com/de/reaction/353159

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperidineHCID 8082—
Edukt1,3,5-TriazineHCID 9262—
Edukt2-Amino-4,5-difluorobenzoic acidHCID 735965—
LösungsmittelEthanolHCID 702—
Produkt6,7-Difluoroquinazolin-4(3H)-oneHCID 13547130886%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06750218B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-26367b7bf5f44bffb86b8d2214bf5dda
Quellennotizuspto-grants-2004_06