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HRID 1008340作成日:2026年10月26日

Chloroform → 4-{[7-(Benzyloxy)-6-methoxy-4-quinazolinyl]oxy}-2-chloroaniline

https://huagongshe.com/reaction/1008340

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroformHCID 6212—
反応物Sodium HydroxideHCID 14798—
反応物7-(Benzyloxy)-4-chloro-6-methoxyquinazolineHCID 10661998—
反応物4-Amino-3-chlorophenol hydrochlorideHCID 12598190—
触媒Tetrabutylammonium ChlorideHCID 70681—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
生成物4-{[7-(Benzyloxy)-6-methoxy-4-quinazolinyl]oxy}-2-chloroanilineHCID 2266723290%

反応手順

7-(Benzyloxy)-4-chloro-6-methoxyquinazoline (30.0 g) and tetrabutylammonium chloride (13.9 g) were dissolved in acetone (400 ml), and the solution was stirred at room temperature. A solution of 4-amino-3-chlorophenol hydrochloride (36.0 g) in a 20% aqueous sodium hydroxide solution (64 ml) was added thereto. The mixture was then heated under reflux for 3 hr. The reaction solution was cooled to room temperature, and chloroform and water were added to the cooled reaction solution, followed by extraction with chloroform. The extract was washed with a saturated aqueous sodium hydrogencarbonate solution and saturated brine and was then dried over anhydrous sodium sulfate. Next, sodium sulfate was removed, and the solvent was then removed by distillation. The residue was washed with methanol, and the washed solid was subjected to evaporation to dryness in vacuo through a vacuum pump to give 36.6 g (yield 90%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06797823B1
出典データセットuspto-grants-2004_09
ORD IDord-2f79078892f0406ba85cbcd90b3c5a14
出典メモuspto-grants-2004_09