関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Amitrole | HCID 1639 | — |
| 反応物 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 反応物 | cis-2,6-dimethyloxan-4-one | HCID 10441716 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | N-[(2R,6S)-2,6-dimethyltetrahydro-2H-pyran-4-yl]-1H-1,2,4-triazol-5-amine | HCID 67008740 | 49% |
反応手順
To a solution of 1H-1,2,4-triazol-5-amine (1.6 g) in acetic acid (30 mL) was added (2R,6S)-2,6-dimethyltetrahydro-4H-pyran-4-one (2.5 g) at room temperature, and the mixture was stirred for 30 min. After stirring, sodium triacetoxyborohydride (5.2 g) was added, and the mixture was stirred at room temperature for 20 hr. Acetic acid was evaporated and ethyl acetate and water were added to the residue. The mixture was neutralized with sodium hydrogen carbonate, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated. The residue was dissolved in a small amount of ethyl acetate, and the mixture was crystallized from diisopropyl ether. The resulting solid was collected by filtration, washed with diisopropyl ether, and dried by heating under reduced pressure to give the title compound as a pale-yellow solid (1.6 g, 49%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09115136B2 |
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| 出典データセット | uspto-grants-2015_08 |
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| ORD ID | ord-597caf5348ae442e8ad6c22644bf03d0 |
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| 出典メモ | uspto-grants-2015_08 |
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