化工社化工社 化学情報印刷レポート · 研究参考用
[7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridin-2-yl]methanol → 7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridine-2-carboxaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | [7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridin-2-yl]methanol | HCID 68981956 | — |
| 触媒 | HCID 178418406 | HCID 178418406 | — |
| 溶媒 | Methyl, chloro- | HCID 5378701 | — |
| 生成物 | 7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridine-2-carboxaldehyde | HCID 57893503 | 60% |
反応手順
[7-(Dibenzylamino)-1H-pyrrolo[2,3-c]pyridin-2-yl]methanol (3.0 g, 8.74 mmol) was dissolved in methylene chlorine (175 mL). Manganese dioxide (8.0 g, 92 mmol) was added and the reaction mixture was stirred at room temperature for 20 h. The slurry was filtered through diatomaceous earth to remove the catalyst, and the filtrate was concentrated to a dark oil. Purification by Biotage chromatography (10-30% ethyl acetate in hexanes) provided 7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridine-2-carboxaldehyde (1.78 g, 60%) as a yellow oil: 1H NMR (300 MHz, CDCl3) δ4.89 (4H, s), 7.06-7.12 (2H, m), 7.27-7.38 (10H, m), 7.93 (1H, d, J=5.7 Hz), 8.74 (1H, br s), 9.77 (1H, s).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07608627B2 |
| 出典データセット | uspto-grants-2009_10 |
| ORD ID | ord-c1c4f3fb22ea4648afcab6b4086067e5 |
| 出典メモ | uspto-grants-2009_10 |