Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1005519생성일: 2026년 10월 26일
Triethylamine → 2-(1-Butoxycyclopentyloxy)methyl-5-(3,5-dichlorophenylthio)-4-isopropyl-1-ethyl-1H-imidazole
https://huagongshe.com/reaction/1005519
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1,1-Dibutoxycyclohexane | HCID 243718 | — |
| 반응물 | (5-(3,5-Dichlorophenylthio)-1-ethyl-4-isopropyl-1H-imidazol-2-yl)methanol | HCID 473933 | — |
| 반응물 | Pyridinium.p-toluenesulfonate | HCID 22033616 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-(1-Butoxycyclopentyloxy)methyl-5-(3,5-dichlorophenylthio)-4-isopropyl-1-ethyl-1H-imidazole | HCID 53719220 | 34% |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06054591 |
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| 출처 데이터셋 | uspto-grants-2000_04 |
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| ORD ID | ord-5b3f7ad41dbf4aa48d176520476b5aad |
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| 출처 메모 | uspto-grants-2000_04 |
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