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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 859701Erstellt: 26. Oktober 2026

Ethyl bromopyruvate → Imidazo[1,2-b][1,2,4]triazine-carboxylic acid ethyl ester

https://huagongshe.com/reaction/859701

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl bromopyruvateHCID 66144—
Edukt3-Amino-1,2,4-triazineHCID 70715—
LösungsmittelEthanolHCID 702—
ProduktImidazo[1,2-b][1,2,4]triazine-carboxylic acid ethyl esterHCID 695885131,8%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07151105B2
Quelldatensatzuspto-grants-2006_12
ORD IDord-b58162468cf648cfb6a71d2c4072f883
Quellennotizuspto-grants-2006_12