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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2170801Erstellt: 25. Oktober 2026

4-Chlorobenzamidine → 2-(4-Chloro-phenyl)-5-methyl-3H-pyrimidin-4-one

https://huagongshe.com/reaction/2170801

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-ChlorobenzamidineHCID 203437—
EduktSodiumHCID 5360545—
EduktEthyl 2-FormylpropionateHCID 10898741—
LösungsmittelEthanolHCID 702—
Produkt2-(4-Chloro-phenyl)-5-methyl-3H-pyrimidin-4-oneHCID 5990661152%

Reaktionsschritte

Sodium metal (276 mg, 12 mmol) was added portion wise to ethanol (15 ml) under a nitrogen atmosphere and the mixture allowed to stir at room temperature for 30 minutes until the reaction became homogeneous. 4-Chloro-benzamidine (hydroiodide salt) (1.41 g, 5 mmol) was then added in one portion and the reaction stirred at room temperature for a further 60 minutes. 2-Methyl-3-oxo-propionic acid ethyl ester (716 mg, 5.5 mmol) was finally added drop wise. The reaction was left to stir at room temperature overnight before quenching the reaction slowly with 2M Hydrochloric acid until reaction pH measured pH 1. The resulting precipitate was filtered and air dried, to give 2-(4-Chloro-phenyl)-5-methyl-3H-pyrimidin-4-one as a white solid (570 mg, 2.58 mmol, 52% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09051300B2
Quelldatensatzuspto-grants-2015_06
ORD IDord-03928676cd9942beab34293893f99084
Quellennotizuspto-grants-2015_06