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Article 2023 · 1 atıf

Synthesis of novel pyrazole-4-carboxylates by rearrangement reaction: Experimental and theoretical characterization

Korkusuz, Elif, Sert, Yusuf, Sahin, Ertan, Yildirim, Ismail, Koca, Irfan

Özet

In this study, alkyl pyrazole-4-carboxylate compounds (5a-d) were synthesized from the esterification reaction of pyrazole-5-carboxylic acid compound by rearrangement. Molecules 5a-d have been studied in detail both experimentally (x-ray, FT-IR and NMR) and theoretically. Optimization of the structure for all compounds, Highest Occupied Molecular Orbital (HOMO)-Lowest Unoccupied Molecular Orbital (LUMO) values and distributions and Molecular Electrostatic Potential (MEP) analyzes for only 5d (most stable energy and single crystal) were performed by DFT theory at B3LYP functional and 6-311++G(d,p) basis set. Possible crystallization of the structure (5d) from experimental crystal was carried out by Hirshfeld surface analysis. In the next step, the interactions between the 5a, 5b, 5c and 5d molecules, the proposed molecule from the similarity and the target were made by molecular docking calculations. Then, drug-likeness and ADME properties were investigated.

Anahtar Kelimeler
Pyrazole Rearrangement reaction DFT Hirshfeld surface analysis Molecular docking HIRSHFELD SURFACE-ANALYSIS HOMO-LUMO GAP MOLECULAR DOCKING SUPRAMOLECULAR SYNTHONS PYRAZOLE DERIVATIVES CRYSTAL-STRUCTURES DRUG DISCOVERY FT-IR CRYSTALEXPLORER PERFORMANCE
WoS Kategorileri
Chemistry, Multidisciplinary Physics, Condensed Matter
Sürdürülebilir Kalkınma Amaçları
Künye
Dergi
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS
Yıl
2023
Cilt
181
ISSN
0022-3697
eISSN
1879-2553
DOI
10.1016/j.jpcs.2023.111536
WoS UID
WOS:001034473200001
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