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HRID 68158作成日:2026年10月25日

Sodium Iodide → methyl 3-{2-[5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]ethylsulfanyl}propionate

https://huagongshe.com/reaction/68158

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物DimethylformamideHCID 6228—
反応物Methyl 3-mercaptopropionateHCID 18050—
反応物1-(2-Chloroethyl)-5-fluoro-3-(4-methoxyphenyl)-8-propoxy-1H-quinolin-4-oneHCID 58492557—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物methyl 3-{2-[5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]ethylsulfanyl}propionateHCID 5849249675.2%

反応条件

温度80 °C

反応手順

1-(2-Chloroethyl)-5-fluoro-3-(4-methoxyphenyl)-8-propoxy-1H-quinolin-4-one (3.5 g, 8.98 mmol), methyl 3-mercaptopropionate (1.19 g, 9.88 mmol), and sodium iodide (1.48 g, 9.88 mmol) were added to DMF (30 ml) and stirred at 80° C. for 5 hours. Water and ethyl acetate were added to the reaction mixture, followed by separation. The thus-obtained organic layer was washed with water, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified using silica gel column chromatography (dichloromethane). The purified product was concentrated to dryness under reduced pressure, giving a pale yellow powder of methyl 3-{2-[5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]ethylsulfanyl}propionate (3.2 g, yield: 75%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE045108E1
出典データセットuspto-grants-2014_09
ORD IDord-ae0d3f04578741a88bffe5a0a1aebf30
出典メモuspto-grants-2014_09