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HRID 617123作成日:2026年10月27日

Acetic Acid → 3-[4-(2-chloro-ethoxy)-phenyl]-7-methoxy-2-(4methoxy-phenyl)-2,3-dihydro-1H-quinazolin-4-one

https://huagongshe.com/reaction/617123

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物4-MethoxybenzaldehydeHCID 31244—
反応物2-Amino-N-[4-(2-chloro-ethoxy)-phenyl]-4-methoxy-benzamideHCID 21851086—
溶媒EthanolHCID 702—
生成物3-[4-(2-chloro-ethoxy)-phenyl]-7-methoxy-2-(4methoxy-phenyl)-2,3-dihydro-1H-quinazolin-4-oneHCID 21851080—

反応手順

To a solution of 14.9 g (0.0465 mol) of 2-amino-N-[4-(2-chloro-ethoxy)-phenyl]-4-methoxy-benzamide in 300 mL of ethanol was added 5.6 mL (0.0465 mol) of p-anisaldehyde and 30 mL of acetic acid. The reaction mixture was stirred and heated under a mild reflux overnight. After cooling to room temperature, the solvent was evaporated in a rotary evaporator. After the addition of diethyl ether and petroleum ether, the oily residue was chilled on ice. The precipitate that formed was collected by vacuum filtration. An analytical sample (mp 157-158° C. was obtained by recrystallization from ethanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05948775
出典データセットuspto-grants-1999_09
ORD IDord-9c27583fb6b6467e805c4b8479c0dfba
出典メモuspto-grants-1999_09