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Piperidine → 6,7-Difluoroquinazolin-4(3H)-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Piperidine | HCID 8082 | — |
| 反応物 | 1,3,5-Triazine | HCID 9262 | — |
| 反応物 | 2-Amino-4,5-difluorobenzoic acid | HCID 735965 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 6,7-Difluoroquinazolin-4(3H)-one | HCID 135471308 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06750218B2 |
| 出典データセット | uspto-grants-2004_06 |
| ORD ID | ord-26367b7bf5f44bffb86b8d2214bf5dda |
| 出典メモ | uspto-grants-2004_06 |