化工社化工社 化学情報印刷レポート · 研究参考用
Piperazine → 4-(Piperazin-1-yl)thieno[3,2-c]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Piperazine | HCID 4837 | — |
| 反応物 | 4-Chlorothieno[3,2-c]pyridine | HCID 12827312 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 4-(Piperazin-1-yl)thieno[3,2-c]pyridine | HCID 10966027 | 56.1% |
反応手順
A mixture of 4-chlorothieno[3,2-c]pyridine (22.7 g, 0.13 mole) and piperazine (57.7 g, 0.67 mole) were heated in a bomb with a minimum amount of ethanol (50 mL) at 120° for 24 hours. The reaction was cooled, partitioned between dichloromethane and water, and the organic layer was isolated, dried (MgSO4), filtered, and concentrated in vacuo to an oil. Flash chromatography (methylene chloride-10% methanol-1% ammonium hydroxide) of this material gave 16 g (54%) of a golden oil. Treatment of an ethanol solution of the oil with ethanolic HCl followed by recrystallization from ethanol gave the hydrochloride salt as off-white crystals, m.p. 275°-283°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04677104 |
| 出典データセット | uspto-grants-1987_06 |
| ORD ID | ord-835e7b028b934112bcad12d39be926bf |
| 出典メモ | uspto-grants-1987_06 |