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HRID 353159作成日:2026年10月25日

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

https://huagongshe.com/reaction/353159

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物1,3,5-TriazineHCID 9262—
反応物2-Amino-4,5-difluorobenzoic acidHCID 735965—
溶媒EthanolHCID 702—
生成物6,7-Difluoroquinazolin-4(3H)-oneHCID 13547130886%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06750218B2
出典データセットuspto-grants-2004_06
ORD IDord-26367b7bf5f44bffb86b8d2214bf5dda
出典メモuspto-grants-2004_06