化工社化工社 化学情報印刷レポート · 研究参考用
Acetaldehyde → 3-Diethylaminopyrazolo[1,5-a]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetaldehyde | HCID 177 | — |
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | Sodium cyanoborohydride | HCID 5003444 | — |
| 反応物 | Pyrazolo[1,5-a]pyridin-3-amine | HCID 12068469 | — |
| 生成物 | 3-Diethylaminopyrazolo[1,5-a]pyridine | HCID 69588332 | 58% |
反応手順
A solution of 3-aminopyrazolo[1,5-a]pyridine (0.74 g, 5.55 mmol) in acetonitrile (15.0 mL) was treated with acetaldehyde (6.2 mL, 4.89 g, 111 mmol) and NaCNBH3 (0.84 g, 13.3 mmol) and stirred at room temperature for 3 days. The reaction was concentrated in vacuo and the residue partitioned between ethyl acetate and saturated NaHCO3 solution. The layers were separated and the aqueous layer was extracted with ethyl acetate (2×). The organic layers were combined, washed with brine, dried over MgSO4 and concentrated in vacuo to dryness. The residue was subjected to column chromatography (15% ethyl acetate/hexane) to give 0.61 g (58%) of a yellow oil as the title compound: MS (EI) m/z 190 (M++H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07151109B2 |
| 出典データセット | uspto-grants-2006_12 |
| ORD ID | ord-3c34ae03cc5f4b118e79cf6d7ffce70d |
| 出典メモ | uspto-grants-2006_12 |