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Research Journal of Pharmacy and Technology
Year : 2021, Volume : 14, Issue : 7
First page : ( 3921) Last page : ( 3926)
Print ISSN : 0974-3618. Online ISSN : 0974-360X.
Article DOI : 10.52711/0974-360X.2021.00681

Iodine -a versatile reagent for vinylogous mannich reaction for the synthesis of 8-amino y-butenolides and Insilico evaluation

Nagamani C.1,*, Sherisha D.1, Sumalatha K.1, Sowjanya M.2

1Department of Pharmaceutical Chemistry, Bhaskar Pharmacy College, Telangana, India

2Department of Chemistry, Vijaya Teja Degree College, Addanki, Andhra Pradesh, India

*Corresponding Author E-mail: manisunil212@gmail.com

Online published on 25 August, 2021.

Abstract

A set of 5-amino y-butenolides (1–5) were synthesised by a novel method using molecular iodine as a catalyst by mannich reaction. The purity and progress of the reaction was assessed by thin layer chromatography and the compounds characterisation was done by IR, proton NMR and mass spectroscopic techniques. Molecular modeling studies for the compounds such as docking was performed for the synthesized butenolides to understand the drug receptor interactions and analyze structural changes when bound to the active site of the receptor. the results showed that the compounds 2 and 3 showed significant interaction with target enzymes.

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Keywords

5-amino y-butenolides, Molecular iodine, Molecular modeling, MOL GRO virual docker.

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