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2-(2-Azabicyclo[2.2.2]oct-2-yl)-6-nitroquinoline → 2-(2-Azabicyclo[2.2.2]oct-2-yl)quinolin-6-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-(2-Azabicyclo[2.2.2]oct-2-yl)-6-nitroquinoline | HCID 22018884 | — |
| 触媒 | Palladium hydroxide | HCID 9942167 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 2-(2-Azabicyclo[2.2.2]oct-2-yl)quinolin-6-amine | HCID 22018930 | — |
反応手順
The product of Step A and palladium hydroxide on carbon (1.3 g, 20% by wt) was suspended in methanol (100 mL) and ethyl acetate (100 mL). The resulting mixture was degassed then stirred under hydrogen atmosphere (balloon) for 6 h. The reaction mixture was filtered through filter aid and the solvent removed under vacuum. The resulting oil was dissolved in ethyl acetate and the solvent removed under vacuum. The resulting oil was suspended in ether and triturated until crystallization occurred. The solids were filtered and washed with ice-cold ether then dried under vacuum to afford the product as a brown solid, MS: m/z 254 (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-941df1acbb1249ef9c18b030f6937c2a |
| 出典メモ | uspto-grants-2006_08 |