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HRID 1837363作成日:2026年10月27日

2-Methoxyethanol → 4-[(2,4-Dichloro-5-methoxyphenyl)amino]-6-methoxy-7-(2-methoxyethoxy)quinoline-3-carbonitrile

https://huagongshe.com/reaction/1837363

反応式

関与物質

役割名称HCID仕込み量
反応物2-MethoxyethanolHCID 8019—
反応物SodiumHCID 5360545—
反応物4-[(2,4-Dichloro-5-methoxyphenyl)amino]-7-fluoro-6-methoxy-3-quinolinecarbonitrileHCID 11486153—
生成物4-[(2,4-Dichloro-5-methoxyphenyl)amino]-6-methoxy-7-(2-methoxyethoxy)quinoline-3-carbonitrileHCID 5330110—

反応条件

温度125 °C

反応手順

A mixture of sodium (118 mg, 5.11 mmol) and 2-methoxyethanol (5 mL) is heated at 120-130° C. for 3 hours. 4-[(2,4-Dichloro-5-methoxyphenyl)amino]-7-fluoro-6-methoxy-3-quinolinecarbonitrile (500 mg, 1.28 mmol) is added and the reaction mixture is heated at 120-125° C. for 1 hour. The temperature of the reaction mixture is increased to 140-150° C. and this temperature is maintained for 2.5 hours. The reaction mixture is cooled to room temperature and diluted with ice cold aqueous sodium bicarbonate. The solid is collected by filtration washing with water and hexane. Purification by flash column chromatography, eluting with 2% methanol in dichloromethane provides 550 mg of 4-[(2,4-dichloro-5-methoxyphenyl)amino]-6-methoxy-7-[2-methoxyethoxy]-3-quinolinecarbonitrile, mp 210-212° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06780996B2
出典データセットuspto-grants-2004_08
ORD IDord-af770a3ee36f4aa78aca38859b1212ac
出典メモuspto-grants-2004_08