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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2742생성일: 2026년 10월 24일

Triethylamine → 3-[2-(6-Butoxy-3-pyridyl)ethynyl]quinuclidin-3-ol

https://huagongshe.com/ko/reaction/2742

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Ethynyl-1-azabicyclo[2.2.2]octan-3-olHCID 3613517—
반응물5-Bromo-2-butoxypyridineHCID 18936268—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매DimethylformamideHCID 6228—
생성물3-[2-(6-Butoxy-3-pyridyl)ethynyl]quinuclidin-3-olHCID 994827825.2%

반응 조건

온도90 °C

반응 단계

A stirred mixture of 3-ethynyl-3-hydroxyquinuclidine (600 mg), 5-bromo-2-n-butoxypyridine (920 mg), bis-(triphenylphosphine)-palladium (II) chloride (140 mg), copper (I) iodide (70 mg) and dry triethylamine (10 ml) in dry dimethylformamide (20 ml) was heated at 90° C. under an atmosphere of argon for 6 hours. The reaction mixture was cooled and the dimethylformamide and triethylamine were removed by evaporation. The residue was treated with 2M aqueous sodium hydroxide solution (20 ml) and the resulting mixture extracted with dichloromethane (3×20 ml). The organic extracts were combined, dried (MgSO4) and evaporated to give a brown residue which was crystallised from acetonitrile to yield 3-[2-(6-butoxy-3-pyridyl)ethynyl]quinuclidin-3-ol (300 mg) as a solid, m.p. 149°-151° C.; microanalysis, found: C, 71.3; H, 7.9; N, 8.9%; C18H24N2O2 0.1H 2O requires: C, 71.47; H, 8.08; N, 9.26%; NMR (DHSOd6): 0.9-1.0(3H, t), 1.2-1.35(1H, m), 1.35-1.5(2H, m), 1.5-1.65(1H, m), 1.65-1.75(2H, m), 1.75-2.0(3H, m), 2.6-2.75(4H, t), 2.8-2.85(1H, d), 3.02-3.17(1H, d), 4.2-4.3(2H, t), 5.55(1H, s), 6.75-6.83(1H, d), 7.65-7.72(1H, d) and 8.2(1H, s); m/Z 301 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731323
출처 데이터셋uspto-grants-1998_03
ORD IDord-c6c10cd15dfc4d01b84ec18ab3764f16
출처 메모uspto-grants-1998_03