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HRID 1005519作成日:2026年10月27日
Triethylamine → 2-(1-Butoxycyclopentyloxy)methyl-5-(3,5-dichlorophenylthio)-4-isopropyl-1-ethyl-1H-imidazole
https://huagongshe.com/reaction/1005519
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 1,1-Dibutoxycyclohexane | HCID 243718 | — |
| 反応物 | (5-(3,5-Dichlorophenylthio)-1-ethyl-4-isopropyl-1H-imidazol-2-yl)methanol | HCID 473933 | — |
| 反応物 | Pyridinium.p-toluenesulfonate | HCID 22033616 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-(1-Butoxycyclopentyloxy)methyl-5-(3,5-dichlorophenylthio)-4-isopropyl-1-ethyl-1H-imidazole | HCID 53719220 | 34% |
反応手順
To a solution of 2-hydroxymethyl-5-(3,5-dichlorophenylthio)-4-isopropyl-1-ethyl-1H-imidazole (19) (345 mg, 1 mmol) prepared in accordance with the method as described in WO 96/10019 (EXAMPLE 25) and p-toluenesulfonic acid pyridinium (264 mg, 1.05 mmol) in methylene chloride (5 ml) was added 1,1-dibutoxycyclohexane (2.14 g, 10.0 mmol), and stirred at room temperature for 20 hours. A drop of triethylamine was added to the reaction mixture , and the mixture was filtered to remove the precipitated insoluble matter. The filtrate was concentrated under reduced pressure. Hexane was added to the residue, and the mixture was filtered to remove the insoluble matter. The filtrate was purified by chromatography on an alumina column (eluate: toluene) to give the compound 20 (165 mg, 34%). Rf 0.41 (Al2O3 60, Type E, toluene).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06054591 |
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| 出典データセット | uspto-grants-2000_04 |
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| ORD ID | ord-5b3f7ad41dbf4aa48d176520476b5aad |
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| 出典メモ | uspto-grants-2000_04 |
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