Abstract
Background: Thiosemicarbazones containing mono- or disaccharide moieties reveal several various remarkable biological activities; therefore these compounds have been focused in organic syntheses. Sydnone ring is the potential basic pharmacodynamic nucleus, which has been reported to possess a wide variety of biological activities such as antitumor, anticancer, anti-inflammatory, antiviral, and scavenging activities. The connection of monosaccharide moiety to sydnone ring could initiate the new activities.
Methods: The synthetic reaction of different substituted 3-phenyl-4-formylsydnone N-(tetra-O-acetyl-β- D-galactopyranosyl)thiosemicarbazones was carried out under microwave-assisted heating conditions. The structures of obtained thiosemicarbazones were confirmed by IR, NMR and mass spectra. All obtained thiosemicarbazones were screened for DPPH radical scavenging ability.
Results: Some different substituted 3-formyl-4-phenylsydnones were prepared by Vilsmeier-Haackʹs formylation reaction. These substituted 4-formylsydnones were converted into corresponding thiosemicarbazones by condensation with N-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)thiosemicarbazide. Some of these thiosemicarbazones showed remarkable DPPH radical scavenging ability.
Conclusion: The efficient synthesis of 3-phenyl-4-formylsydnone N-(tetra-O-acetyl-β-D-galactopyranosyl) thiosemicarbazones under microwave-assisted refluxing conditions has been reported. Reaction yields were 40-80%. Obtained results showed that the compounds 4f and 4g have high antioxidant activity.
Keywords: D-Galactose, DPPH radical, 4-Formylsydnone, thiosemicarbazide, microwave-assisted.
Graphical Abstract
Letters in Organic Chemistry
Title:Reaction of Some Substituted 3-Aryl-4-formylsydnones with Tetra-Oacetyl- β-D-galactopyranosyl)thiosemicarbazide
Volume: 13 Issue: 8
Author(s): Nguyen Dinh Thanh, Hoang Thanh Duc, Nguyen Hoang Minh Hue and Hoang Thi Kim Van
Affiliation:
Keywords: D-Galactose, DPPH radical, 4-Formylsydnone, thiosemicarbazide, microwave-assisted.
Abstract: Background: Thiosemicarbazones containing mono- or disaccharide moieties reveal several various remarkable biological activities; therefore these compounds have been focused in organic syntheses. Sydnone ring is the potential basic pharmacodynamic nucleus, which has been reported to possess a wide variety of biological activities such as antitumor, anticancer, anti-inflammatory, antiviral, and scavenging activities. The connection of monosaccharide moiety to sydnone ring could initiate the new activities.
Methods: The synthetic reaction of different substituted 3-phenyl-4-formylsydnone N-(tetra-O-acetyl-β- D-galactopyranosyl)thiosemicarbazones was carried out under microwave-assisted heating conditions. The structures of obtained thiosemicarbazones were confirmed by IR, NMR and mass spectra. All obtained thiosemicarbazones were screened for DPPH radical scavenging ability.
Results: Some different substituted 3-formyl-4-phenylsydnones were prepared by Vilsmeier-Haackʹs formylation reaction. These substituted 4-formylsydnones were converted into corresponding thiosemicarbazones by condensation with N-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)thiosemicarbazide. Some of these thiosemicarbazones showed remarkable DPPH radical scavenging ability.
Conclusion: The efficient synthesis of 3-phenyl-4-formylsydnone N-(tetra-O-acetyl-β-D-galactopyranosyl) thiosemicarbazones under microwave-assisted refluxing conditions has been reported. Reaction yields were 40-80%. Obtained results showed that the compounds 4f and 4g have high antioxidant activity.
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Cite this article as:
Thanh Dinh Nguyen, Duc Thanh Hoang, Hue Hoang Minh Nguyen and Van Thi Kim Hoang, Reaction of Some Substituted 3-Aryl-4-formylsydnones with Tetra-Oacetyl- β-D-galactopyranosyl)thiosemicarbazide, Letters in Organic Chemistry 2016; 13 (8) . https://dx.doi.org/10.2174/1570178613666160824104037
DOI https://dx.doi.org/10.2174/1570178613666160824104037 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |

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