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HRID 721091作成日:2026年10月26日
p,alpha-DIMETHYLBENZYL ALCOHOL → 1-(4-Methylphenyl)ethyl N-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2,5-dimethylphenyl}carbamate
https://huagongshe.com/reaction/721091
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | p,alpha-DIMETHYLBENZYL ALCOHOL | HCID 10817 | — |
| 反応物 | Triphosgene | HCID 94429 | — |
| 反応物 | 4-((6,7-Dimethoxyquinolin-4-yl)oxy)-2,5-dimethylaniline | HCID 21890421 | — |
| 反応物 | Toluene triethylamine | HCID 22504574 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 1-(4-Methylphenyl)ethyl N-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2,5-dimethylphenyl}carbamate | HCID 21890036 | 73.3% |
反応手順
4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,5-dimethylaniline (80 mg) was added to toluene/triethylamine=10/1 (8 ml), and the mixture was heated under reflux to prepare a solution. A solution of triphosgene (111 mg) in methylene chloride was then added to the solution, and the mixture was heated under reflux for 15 min. Subsequently, 4-methyl-α-methylbenzyl alcohol (50 mg) was added thereto, and the mixture was further stirred with heating under reflux for 2 hr. After the completion of the reaction, the reaction solution was allowed to cool to room temperature before distilled water was added thereto. The mixture was subjected to separatory extraction with chloroform, followed by washing with a 1 N aqueous hydrochloric acid solution and saturated brine. The washed solution was dried over sodium sulfate and was concentrated. The residue was purified on a column using chloroform/methanol to give the title compound (88mg, yield 68%).
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-f4d8cc99eb694ad49393c5bc975c7366 |
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| 出典メモ | uspto-grants-2006_11 |
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