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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49613생성일: 2026년 10월 23일

4-Vinylpyridine → (R)-(-)-5'-(2-(4-Pyridyl)ethenyl)spiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[2,3-b]pyridine]

https://huagongshe.com/ko/reaction/49613

반응식

참여 물질

역할이름HCID투입량
반응물4-VinylpyridineHCID 7502—
반응물TriethylamineHCID 8471—
반응물Tri-o-tolylphosphineHCID 80271—
반응물(2R)-5'-bromo-3'H-spiro[4-azabicyclo[2.2.2]octane-2,2'-furo[2,3-b]pyridine]HCID 54506690—
촉매palladium(II) acetateHCID 167845—
용매AcetonitrileHCID 6342—
생성물(R)-(-)-5'-(2-(4-Pyridyl)ethenyl)spiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[2,3-b]pyridine]HCID 5375759072%

반응 조건

온도102.5 °C

반응 단계

(R)-(−)-5′-Bromospiro[1-azabicyclo[2.2.2]octane-3,2′(3′H)-furo[2,3-b]pyridine] (295 mg, 1 mmol), 4-vinylpyridine (0.135 mL, 1.25 mmol), palladium(II)acetate (7.2 mg, 0.032 mmol), tri-o-tolylphosphine (38.7 mg, 0.127 mmol), and triethylamine (0.5 mL, 3.6 mmol) in anhydrous acetonitrile (0.5 mL) were combined in a heavy-walled threaded glass tube containing a magnetic stir bar, purged with argon and sealed with a Teflon plug and FETFE O-ring. The mixture was stirred and heated at 100 to 105° C. for 48 hours, cooled to room temperature, dissolved in chloroform (25 mL), washed with saturated aqueous sodium carbonate (2 mL), dried (MgSO4), and evaporated under reduced pressure. Purification by flash chromatography through silica gel (eluting with ammoniated chloroform/methanol, 95:5), followed by recrystallization from acetone afforded the title compound (230 mg, 0.72 mmol, 72%): electrospray MS (m/z, relative intensity) 320 ([MH]+, 100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706878B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-34ce5c0d9f7c4dfd97e2ec1e88b787b9
출처 메모uspto-grants-2004_03