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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25618생성일: 2026년 10월 24일

Imidazole → HCID 178463970, 화합물

https://huagongshe.com/ko/reaction/25618

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물Sodium BicarbonateHCID 516892—
반응물HCID 178464455HCID 178464455—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
생성물HCID 178463970HCID 17846397010.2%

반응 조건

온도50 °C

반응 단계

400 mg (8.4 mmol) trans-N-(4-{5-[Ethyl-(2-hydroxy-ethyl)-amino]-pentyl}-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide were suspended in toluene and evaporated (3×), redissolved in lml DMF and treated with 102.4 mg (1.5 mmol, 1.8 eq) imidazole. At 0° C., 176 mg (11.7 mmol, 1.4 eq) TBDMSCl in 2 ml DMF were added, and the reaction mixture was stirred at 50° C. for 1 h. The solution was added to an aqueous solution of NaHCO3 and extracted with ether. The organic layer was washed with water and brine, and dried over Na2SO4. 509 mg crude trans-N-[4-(5-{[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-ethyl-amino}-pentyl)-cyclohexyl]-N-methyl-4-trifluoromethyl-benzenesulfonamide were isolated as light yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858651B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-cc39c75da0944473b4915be6d02ba9a7
출처 메모uspto-grants-2005_02