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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 81476Erstellt: 24. Oktober 2026

3-Amino-2-pyrazinecarboxylic acid → 3-Amino-pyrazine-2-carboxylic acid methoxy-methylamide

https://huagongshe.com/de/reaction/81476

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Amino-2-pyrazinecarboxylic acidHCID 72656—
Edukt1-HydroxybenzotriazoleHCID 75771—
EduktMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
EduktDiisopropylethylamineHCID 81531—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-Amino-pyrazine-2-carboxylic acid methoxy-methylamideHCID 86634549—

Reaktionsschritte

To a solution of 3-aminopyrazine-2-carboxylic acid (1 g, 7.2 mmol) in DMF (15 ml) is added EDC hydrochloride (1.7 g, 8.6 mmol), HOBt (1.16 g, 8.6 mmol), diisopropylethylamine (3.08 ml, 18 mmol) and N-methoxy-N-methylamine hydrochloride (0.84 g, 8.6 mmol), and the resulting solution is stirred at room temperature for 15 hours. The reaction is concentrated in vacuo, and sat. aq. NaHCO3 (50 ml) is added to the residue. The product is extracted into EtOAc (3×60 ml), washed with sat. aq. NaCl (2×50 ml), dried (MgSO4) and concentrated in vacuo to afford a yellow residue. Purification by flash chromatography (SiO2, 0-5% MeOH in DCM) yields 3-amino-pyrazine-2-carboxylic acid methoxy-methylamide as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846687B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-64858c2c746d45169a84ce8da8f2785a
Quellennotizuspto-grants-2014_09