化工社化工社 化学情報印刷レポート · 研究参考用
Ethyl bromopyruvate → Imidazo[1,2-b][1,2,4]triazine-carboxylic acid ethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl bromopyruvate | HCID 66144 | — |
| 反応物 | 3-Amino-1,2,4-triazine | HCID 70715 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Imidazo[1,2-b][1,2,4]triazine-carboxylic acid ethyl ester | HCID 69588513 | 1.8% |
反応手順
A solution of 3-amino-1,2,4-triazine (5.0 g, 52 mmol) and ethyl bromopyruvate (11 mL, 88 mmol) in ethanol (50 mL) was heated to reflux for 20 minutes. The reaction was cooled to room temperature, and then partitioned between 200 mL of EtOAc and 200 mL of water. The layers were separated, and the organic layer was dried over MgSO4. The solids were removed by filtration, and then the solvent was removed by rotary evaporation. The residue was purified by chromatography (90 g SiO2, 50 to 70% EtOAc in hexanes) to give the desired product (181 mg, 1.8%). MS (ESI): 192.4 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07151105B2 |
| 出典データセット | uspto-grants-2006_12 |
| ORD ID | ord-b58162468cf648cfb6a71d2c4072f883 |
| 出典メモ | uspto-grants-2006_12 |