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HRID 591863作成日:2026年10月26日

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

https://huagongshe.com/reaction/591863

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-DimethoxybenzaldehydeHCID 81747—
反応物2-Amino-5-nitrobenzamideHCID 97665—
反応物Sodium BicarbonateHCID 516892—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物Sodium BisulfiteHCID 23665763—
溶媒DimethylacetamideHCID 31374—
生成物6-amino-2-(3,5-dimethoxy-phenyl)-3H-quinazolin-4-oneHCID 136348062—

反応条件

温度150 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09238640B2
出典データセットuspto-grants-2016_01
ORD IDord-e939b15943194a47b7530321302338fb
出典メモuspto-grants-2016_01