Huynh Nhu * , Nguyen Thi Thu Tram and Tran Hoang Yen

* Corresponding authorHuynh Nhu

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Abstract

Derivatives of 1,4-dihydropyridines are well known as calcium channel modulators for the treatment of cardiovascular disorders. Herein, three 1,4-dihydropyridines were synthesized through the condensation of an aldehyde, a β-ketoester, and ammonium acetate in ethanol with yields ranging from 23 to 59%. Their structures were confirmed by comparison HRMS, NMR spectral data with the literature. The acute oral toxicity study for the synthesized compounds revealed that all compounds were safe up to 2000 mg/kg and no deaths of animals were recorded. 
Keywords: 1, 4-dihydropyridines, acute toxicity, Hantzsch ester, β-ketoester

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References

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