関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Quinoline-2-carbonitrile | HCID 74031 | — |
| 反応物 | Trimethylsilyl cyanide | HCID 82115 | — |
| 反応物 | HCID 178526244 | HCID 178526244 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 5-Hydroxyquinoline-2-carbonitrile | HCID 135743697 | — |
反応手順
Typical procedure to prepare 2-cyanoquinoline from N-oxide: Preparation of 2-cyano-5-hydroxyl-2-quinoline: Trimethylsilyl cyanide (12.4 ml) was added into a solution of 5-hydroxyl-quinoline N-oxide (5 g) with triethylamine (13 ml) in MeCN. After the reaction was stirred at room temperature for 12 hours, solvents were removed under vaccum to provide a residue which was then partitioned between saturated NaHCO3 solution (100 ml) and EtOAc (100 ml). The aqueous solution was then extracted with EtOAc (2×100 ml). And the combined organic layer was dried over anhydrous MgSO4, filtered and concentrated to afford a crude product which purified by silica gel column chromatography to provide 5.3 g of 2-cyano-5-hydroxylquinoline. MS m/z: (M+H)+ calcd for C10H7N2O 171.06, found 171.03. HPLC retention time: 1.22 minutes (column I).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07037913B2 |
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| 出典データセット | uspto-grants-2006_05 |
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| ORD ID | ord-c22a015259ca436997e01b9574af9cee |
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| 出典メモ | uspto-grants-2006_05 |
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