関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3-(4-Bromophenyl)pyridine | HCID 1515241 | — |
| 反応物 | 3-Ethenyl-3-hydroxy-1-azabicyclo[2.2.2]octane | HCID 22620778 | — |
| 触媒 | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| 触媒 | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-[2-(4-[3-Pyridyl]phenyl)ethenyl]-3-hydroxyquinuclidine | HCID 54079241 | 29.7% |
反応手順
A mixture of 3-ethenyl-3-hydroxyquinuclidine (673 mg), 3-(4-bromophenyl)pyridine (1.08 g), bis-(triphenylphosphine)-palladium (II) chloride (140 mg), copper (I) iodide (70 mg), and dimethylformamide (10 ml) was stirred at 130° C. under an atmosphere of argon for 4 hours. The mixture was evaporated and the residue was paritioned between aqueous 2M sodium hydroxide solution (10 ml) and dichloromethane (10 ml). The organic layer was separated, washed with dichloromethane (2×10 ml), dried (MgSO4) and evaporated. The residue was crystallised from acetonitrile to give 3-[2-(4-[3-pyridyl]phenyl)ethenyl]-3-hydroxyquinuclidine (400 mg) as a solid, m.p. 195°-198° C.; microanalysis, found: C, 76.4; H, 7.2; N, 8.6%; C20H22N2O.0.5H2O requires: C, 76.2; H, 7.3; N, 8.9%; NMR (DMSO-d6 +CD3COOD): 1.7-2.15(4H, m), 2.35(1H, m), 3.15-3.4(5H, m), 3.5(1H, d), 6.7(1H, d), 6.9(1H, d), 7.5-7.8(7H, m), 8.15(1H, d); m/Z 307 (M+H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05714496 |
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| 出典データセット | uspto-grants-1998_02 |
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| ORD ID | ord-7e48db0894324707a0c7c9d3c3b3308f |
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| 出典メモ | uspto-grants-1998_02 |
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