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HRID 591725作成日:2026年10月27日

p-Toluenesulfonic acid → 2-(4-(2-hydroxyethoxy)-3,5-dimethylphenyl)-7-methoxyquinazolin-4(3H)-one

https://huagongshe.com/reaction/591725

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2-Amino-4-methoxybenzamideHCID 14023002—
反応物Sodium BisulfiteHCID 23665763—
反応物4-(2-Hydroxyethoxy)-3,5-dimethylbenzaldehydeHCID 28932578—
溶媒DimethylacetamideHCID 31374—
生成物2-(4-(2-hydroxyethoxy)-3,5-dimethylphenyl)-7-methoxyquinazolin-4(3H)-oneHCID 136274047—

反応条件

温度115 °C

反応手順

To a solution of 2-amino-4-methoxy-benzamide (1.00 g, 6.01 mmol) and 4-(2-hydroxy-ethoxy)-3,5-dimethyl-benzaldehyde (1.28 g, 6.59 mmol) in N,N-dimethylacetamide (15 mL) were added NaHSO3 (58.5 wt %, 0.68 g, 6.50 mmol) and p-TSA (0.23 g, 1.20 mmol) and the reaction mixture was stirred at 115° C. for 16 hours, and cooled to room temperature. Solvent was removed under reduced pressure. The residue was diluted with water (50 mL), stirred for 30 minutes, and then filtered. The solid was suspended in dichloromethane (30 mL), stirred for 1 hour, filtered, and dried under vacuum, to give 2-[4-(2-hydroxy-ethoxy)-3,5-dimethyl-phenyl]-7-methoxy-3H-quinazolin-4-one as an off-white solid. Yield: 1.20 g (58%).

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-31ac56b2880f4ce68bb5272b6a9121f7
出典メモuspto-grants-2016_01