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Synthesis of ( Z )-3-Allyl-5-(4-nitrobenzylidene)-2-sulfanylidene-1,3-thiazolidin-4-one and Determination of Its Crystal Structure

Affiliation
Institut UTINAM UMR 6213 CNRS, Université de Franche-Comté, 16, Route de Gray, 25030 Besançon, France
Moreno, Bastien;
ORCID
0000-0001-6194-8899
Affiliation
Institut UTINAM UMR 6213 CNRS, Université de Franche-Comté, 16, Route de Gray, 25030 Besançon, France
Jourdain, Isabelle;
ORCID
0000-0002-5647-8084
Affiliation
Institut UTINAM UMR 6213 CNRS, Université de Franche-Comté, 16, Route de Gray, 25030 Besançon, France
Knorr, Michael;
ORCID
0000-0002-4706-5181
Affiliation
Laboratory of Heterocyclic Chemistry Natural Product and Reactivity (LR11ES39), Department of Chemistry, Faculty of Science of Monastir, University of Monastir, Monastir 5019, Tunisia;
Boudriga, Sarra;
ORCID
0000-0002-4787-2135
Affiliation
Anorganische Chemie, Technische Universität Dortmund, Otto-Hahn Straße 6, 44227 Dortmund, Germany;(C.S.);(T.S.)
Strohmann, Carsten;
Affiliation
Anorganische Chemie, Technische Universität Dortmund, Otto-Hahn Straße 6, 44227 Dortmund, Germany;(C.S.);(T.S.)
Schrimpf, Tobias

To extend the existing library of arylidenerhodanines which display a potential biological activity, 3- N -allylrhodanine 1 was condensed under Knoevenagel conditions with p -nitrobenzaldehyde in acetic acid to afford the π-conjugated heterocyclic compound 3-allyl-5-(4-nitrobenzylidene)-2-sulfanylidene-1,3-thiazolidin-4-one 2 . Compound 2 was characterized by IR and NMR spectroscopy, and its UV-vis spectrum was compared with that of compound 3-allyl-5-(4-methoxybenzylidene)-2-sulfanylidene-1,3-thiazolidin-4-one 3. The molecular structure is ascertained by a single-crystal X-ray diffraction study performed at 100 K.

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