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HRID 859701作成日:2026年10月27日

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

https://huagongshe.com/reaction/859701

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromopyruvateHCID 66144—
反応物3-Amino-1,2,4-triazineHCID 70715—
溶媒EthanolHCID 702—
生成物Imidazo[1,2-b][1,2,4]triazine-carboxylic acid ethyl esterHCID 695885131.8%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07151105B2
出典データセットuspto-grants-2006_12
ORD IDord-b58162468cf648cfb6a71d2c4072f883
出典メモuspto-grants-2006_12