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HRID 721852作成日:2026年10月26日

2-Methylhexanoic Acid → N-{3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N'-(2-methylhexanoyl)thiourea

https://huagongshe.com/reaction/721852

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methylhexanoic AcidHCID 20653—
反応物Thionyl ChlorideHCID 24386—
反応物2-methylhexanoyl ChlorideHCID 3458543—
反応物3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]anilineHCID 11739027—
反応物2-Methylhexanoyl isothiocyanateHCID 21890727—
溶媒EthanolHCID 702—
溶媒TolueneHCID 1140—
生成物N-{3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N'-(2-methylhexanoyl)thioureaHCID 2189027858%

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-methylhexanoic acid (80 mg), and the mixture was heated at 100° C. for one hr. The solvent was removed by distillation, and 2-methylhexanoyl isothiocyanate was prepared using the resultant 2-methylhexanoyl chloride as a starting compound according to the description of the literature. 2-Methylhexanoyl isothiocyanate was dissolved in ethanol (1 ml) to prepare a solution. 3-Chloro-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 (44 mg, yield 58%).

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-0fb699b800a14b92bce820149a6026a2
出典メモuspto-grants-2006_11