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HRID 336721作成日:2026年10月25日

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

https://huagongshe.com/reaction/336721

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Sodium BicarbonateHCID 516892—
反応物4-[(Morpholin-4-yl)methyl]benzaldehydeHCID 2795498—
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5,7-dimethoxy-2-(4-(morpholinomethyl)phenyl)quinazolin-4(3H)-oneHCID 136038005—

反応条件

温度150 °C

反応手順

To a solution of 2-amino-4,6-dimethoxy-benzamide (150 mg, 0.76 mmol) and 4-morpholin-4-ylmethyl benzaldehyde (156 mg, 0.76 mmol) in N,N-dimethyl acetamide (10 mL), NaHSO3 (150 mg, 0.84 mmol) and p-TSA (174 mg, 0.91 mmol) were added and the reaction mixture was heated at 150° C. for 5 h. The reaction mixture was cooled to room temperature, water was added and the mixture was neutralized with NaHCO3. The solvent was removed under reduced pressure to give the crude product, which was purified by column chromatography to give 5,7-dimethoxy-2-(4-(morpholinomethyl)phenyl)quinazolin-4(3H)-one, which was converted to the hydrochloride salt (165 mg, 51%). Selected data: MS (ES) m/z: 382.07; MP 206-208° C. (at decomposition).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889698B2
出典データセットuspto-grants-2014_11
ORD IDord-6e0a664d942f43c194a3ce9759ed41eb
出典メモuspto-grants-2014_11