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HRID 80641作成日:2026年10月23日
Azidomethyl 2,2-dimethylpropanoate → (4-((6-(1H-Tetrazol-1-yl)pyridin-3-yloxy)methyl)-1H-1,2,3-triazol-1-yl)methyl pivalate
https://huagongshe.com/ja/reaction/80641
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Azidomethyl 2,2-dimethylpropanoate | HCID 11521126 | — |
| 反応物 | Water butanol | HCID 22253497 | — |
| 反応物 | Sodium Ascorbate | HCID 23667548 | — |
| 反応物 | 5-(Prop-2-ynyloxy)-2-(1H-tetrazol-1-yl)pyridine | HCID 57708431 | — |
| 触媒 | Copper Sulfate | HCID 24462 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | (4-((6-(1H-Tetrazol-1-yl)pyridin-3-yloxy)methyl)-1H-1,2,3-triazol-1-yl)methyl pivalate | HCID 57708433 | — |
反応手順
To a solution of azidomethyl pivalate (4.26 g, 27.1 mmol) in 1:1 text -butanol water (90 mL total) was added 5-(prop-2-ynyloxy)-2-(1H-tetrazol-1-yl)pyridine (5.45 g, 27.1 mmol), sodium ascorbate (1.4 mL of a 1M solution in water) and copper sulfate (1.4 mL of a 1M solution in water). The solution was stirred at room temperature for 72 hours. Water was added and the suspension was extracted with ethyl acetate. The organic layer was separated, dried over sodium sulfate, filtered and concentrated in vacuo to afford the expected product which was used in the next step without further purification. 1H NMR (DMSO-d6): δ 10.07 (1H, s), 8.43-8.41 (2H, m), 8.00 (1H, d, J=8.8 Hz), 7.88 (1H, dd, J=3.2, 8.8 Hz), 6.32 (2H, s), 5.38 (2H, s), 1.08 (9H, s).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08846675B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-6cb9a023f229469fa1e8821c6da6f32f |
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| 出典メモ | uspto-grants-2014_09 |
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