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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170801Generated: October 25, 2026

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

https://huagongshe.com/reaction/2170801

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzamidineHCID 203437—
ReactantSodiumHCID 5360545—
ReactantEthyl 2-FormylpropionateHCID 10898741—
SolventEthanolHCID 702—
Product2-(4-Chloro-phenyl)-5-methyl-3H-pyrimidin-4-oneHCID 5990661152%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051300B2
Source datasetuspto-grants-2015_06
ORD IDord-03928676cd9942beab34293893f99084
Source noteuspto-grants-2015_06