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HRID 721779作成日:2026年10月25日

2,4-Dimethylbenzoic acid → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N'-(2,4-dimethylbenzoyl)thiourea

https://huagongshe.com/reaction/721779

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-Dimethylbenzoic acidHCID 11897—
反応物Thionyl ChlorideHCID 24386—
反応物2,4-Dimethylbenzoyl chlorideHCID 140867—
反応物4-[(6,7-Dimethoxyquinolin-4-yl)oxy]anilineHCID 11594543—
反応物2,4-Dimethyl-1-benzenecarbonyl isothiocyanateHCID 16778121—
溶媒EthanolHCID 702—
溶媒TolueneHCID 1140—
生成物N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N'-(2,4-dimethylbenzoyl)thioureaHCID 2189087493%

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 2,4-dimethylbenzoic acid (80 mg), and the mixture was heated at 100° C. for one hr. The solvent was removed by distillation, and 2,4-dimethyl-1-benzenecarbonyl isothiocyanate was prepared using the resultant 2,4-dimethyl-1-benzenecarbonyl chloride as a starting compound according to the description of the literature. 4-[(6,7-Dimethoxy-4-quinolyl)oxy]aniline (50 mg) was dissolved in toluene (5 ml) and ethanol (1 ml) to prepare a solution. A solution of 2,4-dimethyl-1-benzenecarbonyl isothiocyanate in ethanol (1 ml) was 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 (77 mg, yield 93%).

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-e6d68adf7f7b4272ae2936c463fba777
出典メモuspto-grants-2006_11