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HRID 721841作成日:2026年10月26日

Thionyl Chloride → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N'-(3-ethoxypropanoyl)thiourea

https://huagongshe.com/reaction/721841

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物3-Ethoxypropionic acidHCID 61351—
反応物4-[(6,7-Dimethoxyquinolin-4-yl)oxy]anilineHCID 11594543—
反応物3-Ethoxypropanoyl chlorideHCID 12425341—
反応物3-Ethoxypropanoyl isothiocyanateHCID 21890477—
溶媒EthanolHCID 702—
溶媒TolueneHCID 1140—
生成物N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N'-(3-ethoxypropanoyl)thioureaHCID 2189073772%

反応条件

温度100 °C

反応手順

Toluene (20 ml) and thionyl chloride (1 ml) were added to commercially available 3-ethoxypropanoic acid (80 mg), and the mixture was heated at 100° C. for one hr. The solvent was removed by distillation, and 3-ethoxypropanoyl isothiocyanate was prepared using the resultant 3-ethoxypropanoyl chloride as a starting compound according to the description of the literature. 3-Ethoxypropanoyl isothiocyanate was dissolved in ethanol (1 ml) to prepare a solution. 4-[(6,7-Dimethoxy-4-quinolyl)oxy]aniline (50 mg), toluene (5 ml), and ethanol (1 ml) were added to the solution, and the mixture was stirred at room temperature for 2 hr. The reaction solution was concentrated, and the residue was purified by chromatography on silica gel using chloroform/acetone for development to give the title compound (55 mg, yield 72%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07135466B2
出典データセットuspto-grants-2006_11
ORD IDord-2c1efa9ef32b4a85bba513680ef3c64b
出典メモuspto-grants-2006_11