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HRID 228037생성일: 2026년 10월 25일

Citric Acid → 4-tert-butoxycarbonylamino-N-(4-chlorophenyl)-N-methylbicyclo[2.2.2]octane-1-carboxamide

https://huagongshe.com/reaction/228037

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물TrichloroacetonitrileHCID 11011—
반응물TriphenylphosphineHCID 11776—
반응물4-Chloro-N-methylbenzenamineHCID 70272—
반응물4-{[(Tert-butoxy)carbonyl]amino}bicyclo[2.2.2]octane-1-carboxylic acidHCID 23150738—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물4-tert-butoxycarbonylamino-N-(4-chlorophenyl)-N-methylbicyclo[2.2.2]octane-1-carboxamideHCID 23150517—

반응 단계

4-tert-Butoxycarbonylaminobicyclo[2.2.2]octane-1-carboxylic acid (101 mg) was dissolved in dichloromethane (2 mL). To this solution, trichloroacetonitrile (74.0 μL) and triphenylphosphine (196 mg) in dichloromethane (1.5 mL) were sequentially added and the mixture was stirred at room temperature for 2 hours. This was followed by addition of triethylamine (0.18 mL) and 4-chloro-N-methylaniline (98.6 μL) and stirring at room temperature for additional 5.5 hours. The reaction mixture was then poured into aqueous citric acid (5 mL) and was extracted with ethyl acetate (3×10 mL). The ethyl acetate extracts were combined, washed with saturated aqueous sodium bicarbonate solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by a silica gel column (eluant:hexane:ethyl acetate=2:1) to give 4-tert-butoxycarbonylamino-N-(4-chlorophenyl)-N-methylbicyclo[2.2.2]octane-1-carboxamide (91.4 mg) as a white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560569B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-3233b079ee80401286c5780430e054a0
출처 메모uspto-grants-2009_07