関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethylenediamine | HCID 3301 | — |
| 反応物 | 2-Methylpyridine-3-carbonitrile | HCID 4738308 | — |
| 反応物 | Sulfur | HCID 5362487 | — |
| 反応物 | Potassium permanganate silicon dioxide | HCID 23697328 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 3-(1H-imidazol-2-yl)-2-methylpyridine | HCID 59198842 | — |
反応手順
2-Methyl-3-pyridinecarbonitrile 1.05 g, ethylenediamine 5 mL and sulfur 71 mg were mixed, and stirred at 120° C. for 24 hours. Cooling it off to room temperature, toluene and water were added to effect phase separation. The aqueous layer was dried to solid under reduced pressure. Thus obtained crude product was mixed with potassium permanganate/silicon dioxide (carried at a ratio of 2.81 g:3.57 g) 6.38 g and acetonitrile 10 mL at room temperature, and stirred (inducing a rapid exothermic reaction). After the exotherm subsided and the reaction liquid was restored to room temperature, the liquid was diluted with 20 mL of ethanol and filtered through Celite. The solvent was distilled off and the residue was recrystallized from ethyl acetate/methanol (10:1) to provide 1.03 g of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08829000B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-c9acd577965d45f4ba22a52ca2776db2 |
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| 出典メモ | uspto-grants-2014_09 |
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