HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethyl bromopyruvate → Imidazo[1,2-b][1,2,4]triazine-carboxylic acid ethyl ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethyl bromopyruvate | HCID 66144 | — |
| Edukt | 3-Amino-1,2,4-triazine | HCID 70715 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Imidazo[1,2-b][1,2,4]triazine-carboxylic acid ethyl ester | HCID 69588513 | 1,8% |
Reaktionsschritte
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)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07151105B2 |
| Quelldatensatz | uspto-grants-2006_12 |
| ORD ID | ord-b58162468cf648cfb6a71d2c4072f883 |
| Quellennotiz | uspto-grants-2006_12 |