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HRID 2742作成日:2026年10月25日

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

https://huagongshe.com/reaction/2742

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-Ethynyl-1-azabicyclo[2.2.2]octan-3-olHCID 3613517—
反応物5-Bromo-2-butoxypyridineHCID 18936268—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
溶媒DimethylformamideHCID 6228—
生成物3-[2-(6-Butoxy-3-pyridyl)ethynyl]quinuclidin-3-olHCID 994827825.2%

反応条件

温度90 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731323
出典データセットuspto-grants-1998_03
ORD IDord-c6c10cd15dfc4d01b84ec18ab3764f16
出典メモuspto-grants-1998_03