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HRID 555570作成日:2026年10月26日

p-Toluenesulfonic acid → 2-(4-benzyloxy-3,5-dimethyl-phenyl)-5,7-dimethoxy-3H-quinazolin-4-one

https://huagongshe.com/reaction/555570

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物4-(Benzyloxy)-3,5-dimethylbenzaldehydeHCID 563557—
反応物2-Amino-4,6-dimethoxybenzamideHCID 20349016—
反応物Sodium BisulfiteHCID 23665763—
溶媒WaterHCID 962—
溶媒DimethylacetamideHCID 31374—
生成物2-(4-benzyloxy-3,5-dimethyl-phenyl)-5,7-dimethoxy-3H-quinazolin-4-oneHCID 13603799579%

反応条件

温度150 °C

反応手順

A mixture of 2-amino-4,6-dimethoxy-benzamide (0.71 g, 3.71 mmol), 3,5-dimethyl-4-benzyloxy benzaldehyde (0.94 g, 3.90 mmol), sodium hydrogensulfite (0.68 g, 3.90 mmol) and p-toluenesulfonic acid (70 mg, 0.37 mmol) in N,N-dimethylacetamide (25 mL) was stirred at 150° C. for 16 h. The reaction mixture was cooled to room temperature and diluted with water (200 mL). The resulting solid was collected by filtration and washed with hexanes to afford 2-(4-benzyloxy-3,5-dimethyl-phenyl)-5,7-dimethoxy-3H-quinazolin-4-one as a white solid (1.2 g, 79%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08053440B2
出典データセットuspto-grants-2011_11
ORD IDord-95bff62bdef84e28bb4981c7a1aba58c
出典メモuspto-grants-2011_11