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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1911747생성일: 2026년 10월 27일

Water → (3,5-Bis-trifluoromethyl-benzyl)-[2-(4-cyclohexylmethyl-piperazin-1-yl)-quinolin-3-ylmethyl]-carbamic acid ethyl ester

https://huagongshe.com/reaction/1911747

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Ethyl chloroformateHCID 10928—
반응물Potassium CarbonateHCID 11430—
반응물(3,5-Bis-trifluoromethyl-benzyl)-[2-(4-cyclohexylmethyl-piperazin-1-yl)-quinolin-3-ylmethyl]-amineHCID 57486818—
용매TetrahydrofuranHCID 8028—
생성물(3,5-Bis-trifluoromethyl-benzyl)-[2-(4-cyclohexylmethyl-piperazin-1-yl)-quinolin-3-ylmethyl]-carbamic acid ethyl esterHCID 5748679181%

반응 단계

Anhydrous potassium carbonate (0.17 g, 1.23 mmol) was added to a solution of (3,5-bis-trifluoromethyl-benzyl)-[2-(4-cyclohexylmethyl-piperazin-1-yl)-quinolin-3-ylmethyl]-amine (0.23 g, 0.4 mmol) in anhydrous THF (5 mL). After stirring 0.5 h, ethyl chloroformate (0.06 mL, 0.6 mmol) was added slowly under a nitrogen atmosphere. After stirring at RT for overnight, water (25 mL) was added, and the mixture was extracted with ethyl acetate (3×25 mL). The combined organic phases were washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo to give a colorless liquid. Purification by silica gel chromatography and eluting with 10-30% ethyl acetate/hexane afforded the desired final product as a viscous liquid (0.206 g, yield: 81%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08604055B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-77d3a94a851d4b9ca8ef47a8b2754b43
출처 메모uspto-grants-2013_12