돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 749147생성일: 2026년 10월 24일

3-Bromo-5-phenylpyridine → Ethyl 6-hydroxy-6-(5-phenyl-3-pyridinyl)-3-azabicyclo[3.2.1]octane-3-carboxylate

https://huagongshe.com/ko/reaction/749147

반응식

참여 물질

역할이름HCID투입량
반응물3-Bromo-5-phenylpyridineHCID 2762904—
반응물Ethyl 6-oxo-3-azabicyclo(3.2.1)octane-3-carboxylateHCID 53302214—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 6-hydroxy-6-(5-phenyl-3-pyridinyl)-3-azabicyclo[3.2.1]octane-3-carboxylateHCID 5748635614.2%

반응 단계

To a solution of 3-bromo-5-phenylpyridine (0.23 g, 1.0 mmol) in THF (5 mL) at ambient temperature was added 2.0 M isopropylmagnesium chloride in THF (0.5 mL). The reaction was stirred for an hour under nitrogen. Then a solution of ethyl 6-oxo-3-azabicyclo[3.2.1]octane-3-carboxylate (0.21 g, 1.0 mmol) in THF (2 mL) was added. The mixture was stirred at ambient temperature overnight, concentrated and quenched with water (1 mL). The mixture was extracted with chloroform (2×10 mL), and the combined extracts were dried over magnesium sulfate, filtered, and concentrated by rotary evaporation. The compound was purified by silica gel column chromatography (1:1 ethyl acetate/hexane) to yield 50 mg of product (13%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07402592B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-89737a3b41aa4b4ca0bdba7e3185248c
출처 메모uspto-grants-2008_07