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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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1,1-DibutoxycyclohexaneHCID 243718—
반응물(5-(3,5-Dichlorophenylthio)-1-ethyl-4-isopropyl-1H-imidazol-2-yl)methanolHCID 473933—
반응물Pyridinium.p-toluenesulfonateHCID 22033616—
용매DichloromethaneHCID 6344—
생성물2-(1-Butoxycyclopentyloxy)methyl-5-(3,5-dichlorophenylthio)-4-isopropyl-1-ethyl-1H-imidazoleHCID 5371922034%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06054591
출처 데이터셋uspto-grants-2000_04
ORD IDord-5b3f7ad41dbf4aa48d176520476b5aad
출처 메모uspto-grants-2000_04