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HRID 721902作成日:2026年10月25日
3,5-Dimethylbenzoic acid → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-phenyl}-N'-(3,5-dimethylbenzoyl)thiourea
https://huagongshe.com/reaction/721902
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3,5-Dimethylbenzoic acid | HCID 10356 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | 3,5-Dimethylbenzoyl Chloride | HCID 81088 | — |
| 反応物 | 4-[(6,7-Dimethoxyquinolin-4-yl)oxy]aniline | HCID 11594543 | — |
| 反応物 | 3,5-Dimethyl-1-benzenecarbonyl isothiocyanate | HCID 16775643 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-phenyl}-N'-(3,5-dimethylbenzoyl)thiourea | HCID 21890018 | 47% |
反応手順
Toluene (20 ml) and thionyl chloride (1 ml) was 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. 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 3,5-dimethyl-1-benzenecarbonyl isothiocyanate in ethanol (1 ml) was then 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 (39 mg, yield 47%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07135466B2 |
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| 出典データセット | uspto-grants-2006_11 |
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| ORD ID | ord-39d7d2021a6c4803a3a713f129fc5114 |
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| 出典メモ | uspto-grants-2006_11 |
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