SYNTHESIS, CHARACTERIZATION, AND ANTICANCER EVALUATION OF NOVEL HETEROCYCLIC DERIVATIVES BEARING PYRAZOLE, PYRIMIDINE, AND ISOXAZOLE RING FROM 4,7-DICHLOROQUINOLINE

In this study, a series of novel heterocyclic compounds were synthesized by incorporating pyrazole, pyrimidine, and isoxazole rings onto the 4,7-dichloroquinoline scaffold.The synthesis was carried out using various reactions, including nucleophilic substitution and cyclization, to obtain the desired heterocyclic compounds.Fouriertransform infrared spectroscopy and elemental analysis were employed to characterize synthesized compounds, enabling accurate structural determination and assessment of purity.The elemental analysis data indicated that the compounds were of high purity, with consistent stoichiometric ratios of carbon, hydrogen, nitrogen, and chlorine, which was essential for the confirmation of their molecular structure.The physical properties, such as melting points, solubility, and stability, were also recorded and found to be in line with the expected behavior of these novel heterocycles.The synthesized compounds

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Publication Details

Published
2025-09-25
DOI
https://doi.org/10.34218/ijcrd_04_02_002
Primary Topic
Synthesis and biological activity
Type
article
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article

SYNTHESIS, CHARACTERIZATION, AND ANTICANCER EVALUATION OF NOVEL HETEROCYCLIC DERIVATIVES BEARING PYRAZOLE, PYRIMIDINE, AND ISOXAZOLE RING FROM 4,7-DICHLOROQUINOLINE

Hiren Doshi, Sarita Chourasia, Harshil Vasoya, Keyur Lad
Synthesis and biological activity
article

SYNTHESIS, CHARACTERIZATION, AND ANTICANCER EVALUATION OF NOVEL HETEROCYCLIC DERIVATIVES BEARING PYRAZOLE, PYRIMIDINE, AND ISOXAZOLE RING FROM 4,7-DICHLOROQUINOLINE

Hiren Doshi, Sarita Chourasia, Harshil Vasoya, Keyur Lad
article en

Abstract

In this study, a series of novel heterocyclic compounds were synthesized by incorporating pyrazole, pyrimidine, and isoxazole rings onto the 4,7-dichloroquinoline scaffold.The synthesis was carried out using various reactions, including nucleophilic substitution and cyclization, to obtain the desired heterocyclic compounds.Fouriertransform infrared spectroscopy and elemental analysis were employed to characterize synthesized compounds, enabling accurate structural determination and assessment of purity.The elemental analysis data indicated that the compounds were of high purity, with consistent stoichiometric ratios of carbon, hydrogen, nitrogen, and chlorine, which was essential for the confirmation of their molecular structure.The physical properties, such as melting points, solubility, and stability, were also recorded and found to be in line with the expected behavior of these novel heterocycles.The synthesized compounds

Vol. 4(2)
Openalex Percentile: Top 80%
Synthesis and biological activity
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