化工社化工社 化学情報印刷レポート · 研究参考用
Triethylamine → 5-Hydroxy-2-(2-tetrahydropyranyl)pyridazin-3(2H)-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 4-Chloro-5-hydroxy-2-(2-tetrahydropyranyl)pyridazin-3(2H)-one | HCID 54704159 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 5-Hydroxy-2-(2-tetrahydropyranyl)pyridazin-3(2H)-one | HCID 57950355 | — |
反応手順
To 14.3 g (62.0 mmol) 4-chloro-5-hydroxy-2-(tetrahydro-pyran-2-yl)-2H-pyridazin-3-one in 200 mL MeOH and 8.71 mL (62.0 mmol) triethylamine is added 5.00 g 10% Pd/C. The reaction mixture is stirred under a hydrogen atmosphere of 1700 hPa at RT for 16 h. The catalyst is removed by filtration and the solvent is evaporated. 200 mL water is added to the residue, the precipitate is collected, washed with water and dried (fraction A, 7.80 g). The aqueous phase is concentrated and the residue is directly added to a reverse HPLC for purification (Waters xbridge; water (0.15% NH4OH)/acetonitril 95:5 to 10:90) to afford fraction B (4.2 g) which is combined with fraction A.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08067590B2 |
| 出典データセット | uspto-grants-2011_11 |
| ORD ID | ord-6d317ded065340298f23bdd2a90c75f2 |
| 出典メモ | uspto-grants-2011_11 |