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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2088096생성일: 2026년 10월 25일

Triethylamine → (1R*,2R*,5S*,6R*)-8-Benzyl-2-[3,5-bis(trifluoromethyl)benzoyloxy]-1-phenyl-6-phenylsulphonyl-8-azabicyclo[3.2.1]octane

https://huagongshe.com/reaction/2088096

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3,5-Bis(trifluoromethyl)benzoyl chlorideHCID 101856—
반응물Sodium BicarbonateHCID 516892—
반응물(1R*,2R*,5S*,6R*)-8-Benzyl-1-phenyl-6-phenylsulphonyl-8-azabicyclo[3.2.1]octan-2-olHCID 69890353—
용매DichloromethaneHCID 6344—
생성물(1R*,2R*,5S*,6R*)-8-Benzyl-2-[3,5-bis(trifluoromethyl)benzoyloxy]-1-phenyl-6-phenylsulphonyl-8-azabicyclo[3.2.1]octaneHCID 8658664369.3%

반응 단계

A solution of (1R*,2R*,5S*,6R*)-8-benzyl-1-phenyl-6-phenylsulphonyl-8-azabicyclo[3.2.1]octan-2-ol (Description 4; 0.98 g, 2.25 mmol), triethylamine (0.6 ml), N,N-dimethylaminopyridine (100 mg) and 3,5-bis(trifluoromethyl)benzoyl chloride (0.6 ml, 3.33 mmol) in dry dichloromethane (10 ml) was stirred at room temperature for 6 days. The reaction mixture treated with saturated aqueous NaHCO3 and extracted with dichloromethane. The combined organic extracts were dried (Na2SO4) and concentrated. The residue was purified by chromatography on silica gel (iso-hexane:ethyl acetate 5-30%) to give the title compound (1.05 g, 69%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06727249B2
출처 데이터셋uspto-grants-2004_04
ORD IDord-5fd95c5c464b49d0a243b45da076a18a
출처 메모uspto-grants-2004_04