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Sodium Bicarbonate → 2-(2-Azabicyclo[2.2.2]oct-2-yl)-6-nitroquinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 2-Chloro-6-nitroquinoline | HCID 10921723 | — |
| 反応物 | 2-Azabicyclo[2.2.2]octane p-toluenesulfonic acid salt | HCID 11403348 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-(2-Azabicyclo[2.2.2]oct-2-yl)-6-nitroquinoline | HCID 22018884 | — |
反応手順
A mixture of 2-chloro-6-nitroquinoline (5.0 g, 24 mmol, Example 1, Step B), 2-azabicyclo[2.2.2]octane p-toluenesulfonic acid salt (10.2 g, 36 mmol) and sodium bicarbonate (5.1 g, 60 mmol) were mixed in absolute ethanol (100 mL) and then heated at reflux for 24 h. The reaction mixture was cooled to r.t., and the solvent removed under vacuum. The solids were taken up in EtOAc (750 mL). The mixture was transferred to a separatory funnel washed with water (3×100 mL) then brine (100 mL). The organic layer was dried over sodium sulfate, filtered and the solvent removed under vacuum to afford the product as a yellow solid, MS: m/z 284 (MH+) which was used without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07084156B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-a3165b7ee2534a77974b2be0553c8d96 |
| 出典メモ | uspto-grants-2006_08 |