化工社化工社 化学情報印刷レポート · 研究参考用
Piperidine → (E)-5-((2,6-Dimethoxystyrylsulfonyl)methyl)-2-methoxy-3-nitropyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Piperidine | HCID 8082 | — |
| 反応物 | 2,6-Dimethoxybenzaldehyde | HCID 96404 | — |
| 反応物 | 2-((6-Methoxy-5-nitropyridin-3-yl)methylsulfonyl)acetic acid | HCID 67994879 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | (E)-5-((2,6-Dimethoxystyrylsulfonyl)methyl)-2-methoxy-3-nitropyridine | HCID 86690905 | — |
反応手順
A solution of 2-((6-methoxy-5-nitropyridin-3-yl)methylsulfonyl)acetic acid (0.29 g, 1 mmol) in dry pyridine (20 mL) was treated with piperidine (2 mL), followed by 2,6-dimethoxybenzaldehyde (0.17 g, 1 mmol). The mixture was refluxed for 6 h, and evaporated to dryness. The residue was purified by column chromatography using a mixture of EtOAc/PE (1:2, v/v) to yield the titled compound. HR-MS (ESI+) m/z 394.8362; C17H18N2O7S requires 394.0835.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08829003B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-2a9ca364a46c485f84a000b022bec748 |
| 出典メモ | uspto-grants-2014_09 |