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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 721795생성일: 2026년 10월 25일

3,5-Dimethylbenzoic acid → N-{3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N'-(3,5-dimethylbenzoyl)thiourea

https://huagongshe.com/reaction/721795

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참여 물질

역할이름HCID투입량
반응물3,5-Dimethylbenzoic acidHCID 10356—
반응물Thionyl ChlorideHCID 24386—
반응물3,5-Dimethylbenzoyl ChlorideHCID 81088—
반응물3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]anilineHCID 11739027—
반응물3,5-Dimethyl-1-benzenecarbonyl isothiocyanateHCID 16775643—
용매EthanolHCID 702—
용매TolueneHCID 1140—
생성물N-{3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N'-(3,5-dimethylbenzoyl)thioureaHCID 2189115597%

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온도100 °C

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Toluene (20 ml) and thionyl chloride (1 ml) were added to commercially available 3,5-dimethylbenzoic acid (80 mg), and the mixture was heated at 100° C. for one hr. The solvent was removed by distillation, and 3,5-dimethyl-1-benzenecarbonyl isothiocyanate was prepared using the resultant 3,5-dimethyl-1-benzenecarbonyl chloride as a starting compound according to the description of the literature. 3,5-Dimethyl-1-benzenecarbonyl 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 (77 mg, yield 97%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135466B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-96974e3ddf1c426c93785169cc167f33
출처 메모uspto-grants-2006_11