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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 353159생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물1,3,5-TriazineHCID 9262—
반응물2-Amino-4,5-difluorobenzoic acidHCID 735965—
용매EthanolHCID 702—
생성물6,7-Difluoroquinazolin-4(3H)-oneHCID 13547130886%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06750218B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-26367b7bf5f44bffb86b8d2214bf5dda
출처 메모uspto-grants-2004_06