<?xml version="1.0" encoding="UTF-8"?><Articles><Article><id>319</id><JournalTitle>SYNTHESIS CHARACTERIZATION AND PHARMACOLOGICAL EVALUATION OF SOME PYRAZOLIDINEDIONE SUBSTITUTED THIOCROMENE DERIVATIVES AS ANTI-INFLAMMATORY AGENTS</JournalTitle><Abstract>All the newly synthesized compounds were characterized by their physical properties and spectral data. The purity of newly
synthesized compounds was confirmed by TLC. Spectral analysis (IR, 1H, 13C NMR and Mass spectrometry) of the
compounds adequately supported the structures of the synthesized compounds. The appearance of a band between 1764-1623
cm-1 (C=O) in the IR spectra; a singlet peak at ? value 4.3-5.0 for two protons of CH2 of the pyrazolidinedione ring in the 1H
NMR spectra and a peak at ? 41.7-46.9 for carbon of CH2 of the pyrazolidinedione ring supports the formation of
pyrazolidinedione substituted thiochromene derivatives (20-35). Molecular ion peaks of the synthesized pyrazolidinedione
substituted thiochromene derivatives were obtained on the mass spectra, corresponds with their structures. These spectral data
satisfactorily supports the formation of the title compounds.
The formation of thiochromene and pyrazolidinedione moieties is supported by the reaction mechanism</Abstract><Email>ketki492@gmail.com</Email><articletype>Research</articletype><volume>14</volume><issue>2</issue><year>2024</year><keyword> Pyrazolidinedione Ring, Anti-Inflammatory, Synthesis, TLC, NMR.</keyword><AUTHORS>Lucky Tiwari1, Ketkee Mandawar1*, Vibha Devi, Nishi Prakash Jain1</AUTHORS><afflication>RKDF College of Pharmacy, Bhopal</afflication></Article></Articles>