関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Imidazole | HCID 795 | — |
| 反応物 | Lithium hydride | HCID 62714 | — |
| 反応物 | 2-Bromopyridine 1-oxide hydrochloride | HCID 2724044 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-(1-Imidazolyl)pyridine N-oxide | HCID 69108575 | — |
反応手順
A 0.76 g portion of imidazole was added to 7 ml of N,N-dimethylformamide and mixed with 0.2 g of 90% lithium hydride under ice-cooling and then the mixture was stirred for 40 minutes. Next, 2.17 g of 2-bromopyridine N-oxide hydrochloride was gradually added thereto, the mixture was stirred at room temperature for about 1 hour and further heated at 80° C. for about 1 hour, and then the solvent was evaporated and the thus obtained mixture was subjected to a silica gel column chromatography and eluted with chloroform-methanol-28% aqueous ammonia (10:0.9:0.1, v/v/v) to obtain 1.21 g of the title compound as light yellow crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06673799B1 |
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| 出典データセット | uspto-grants-2004_01 |
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| ORD ID | ord-4364c2c3a9a24ba9aa51ccf6def7c34c |
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| 出典メモ | uspto-grants-2004_01 |
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