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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25166Erstellt: 24. Oktober 2026

Acetic Acid → Ethyl imidazo(1,2-c)pyrimidine-7-carboxylate

https://huagongshe.com/de/reaction/25166

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt1H-imidazole-2-carbaldehydeHCID 24955—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
EduktEthyl isocyanoacetateHCID 533707—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktEthyl imidazo(1,2-c)pyrimidine-7-carboxylateHCID 22566015—

Reaktionsschritte

To a suspension of imidazole-2-carboxaldehyde (2.3 g, 23.4 mmol) in 50 mL dioxane is added to ethyl isocyanoacetate (2.9 g, 25.8 mmol) and DBU (3.9 g, 25.8 mmol). After stirring at RT for 5 days, the reaction is neutralized with 10% AcOH. The solvent is removed in vacuo. The residue is taken up in EtOAc/H2O, the aqueous layer is extracted with CHCl3, dried (MgSO4), filtered and concentrated. The residue is purified by chromatography (Biotage 40M, eluting with 5% MeOH/EtOAc). Ethyl imidazo[1,2-c]pyrimidine-7-carboxylate is obtained (1.4 g, 32%) as an off-white solid. 1H NMR (400 MHz, CDCl3) δ9.14, 8.43, 7.88, 7.81, 4.54-4.48, 1.49-1.44.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858613B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-75566e8a19114934948489b12d480eb1
Quellennotizuspto-grants-2005_02