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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 591863생성일: 2026년 10월 25일

3,5-Dimethoxybenzaldehyde → 6-amino-2-(3,5-dimethoxy-phenyl)-3H-quinazolin-4-one

https://huagongshe.com/reaction/591863

반응식

참여 물질

역할이름HCID투입량
반응물3,5-DimethoxybenzaldehydeHCID 81747—
반응물2-Amino-5-nitrobenzamideHCID 97665—
반응물Sodium BicarbonateHCID 516892—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물Sodium BisulfiteHCID 23665763—
용매DimethylacetamideHCID 31374—
생성물6-amino-2-(3,5-dimethoxy-phenyl)-3H-quinazolin-4-oneHCID 136348062—

반응 조건

온도150 °C

반응 단계

A mixture of 2-amino-5-nitro-benzamide (1.81 g, 10.0 mmol), 3,5-dimethoxy-benzaldehyde (1.83 g, 11.0 mmol), sodium hydrogen sulfite (58.5 wt %, 3.94 g, 22.0 mmol), and p-toluenesulfonic acid monohydrate (0.38 g, 2.00 mmol) in N,N-dimethylacetamide (20 mL) was stirred at 150° C. for 17 hours under nitrogen and then cooled to room temperature. Saturated aqueous NaHCO3 (approximately 1 mL) was added. The mixture was stirred at room temperature for 2 hours, then concentrated to dryness. Water (80 mL) was added, stirred for 0.5 hours, and filtered. The solid was air dried. The crude compound was purified by column chromatography (silica gel 230-400 mesh; ethyl acetate as eluent) to give 6-amino-2-(3,5-dimethoxy-phenyl)-3H-quinazolin-4-one as a yellow solid. Yield: 1.50 g (50%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09238640B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-e939b15943194a47b7530321302338fb
출처 메모uspto-grants-2016_01