Significance of Microwave Irradiation in Synthesis of Thiazolidin-4-one Bearing Pyrimidine Analogues: Their in vitro Antimicrobial, Antituberculosis and Antimalarial Studies
{"title":"Significance of Microwave Irradiation in Synthesis of Thiazolidin-4-one Bearing Pyrimidine Analogues: Their in vitro Antimicrobial, Antituberculosis and Antimalarial Studies","authors":"N. Patel, Hetal I. Soni, R. Parmar","doi":"10.2174/2213335607999200918155613","DOIUrl":null,"url":null,"abstract":"\n\nTo synthesise biologically active thiazolidin-4-one by microwave irradiation\nmethod and evaluate against different species of bacteria, fungi and Plasmodium falciparum.\n\n\n\nMicrowave irradiation method is serviceable for rapid and sustainable synthesis. In\nthis present study, Thiazolidin-4-one bearing pyrimidine derivatives have been synthesized by microwave\nirradiation method.\n\n\n\nThiazolidin-4-one is a valuable motif because of its broad-spectrum biological evaluation.\nIt is famous for many types of biological profiles, mainly antimicrobial, anti-tuberculosis, anti-\nconvulsant, antihypertensive, hypoglycemic agent and antimalarial. This biological response\nleads our attention towards the change of Thiazolidin-4-one skeleton to enhance potential. Present\nstudy aims to carry out a rapid synthesis of Thiazolidin-4-one derivative of pyrimidine by microwave-\nassisted heating.\n\n\n\n4-(4-substituted phenyl)-6-(substituted aryl) pyrimidin-2-amine was the key intermediate\nrequired for the synthesis of 3-(4-(Substituted phenyl)-6-(substituted aryl) pyrimidin-2-yl)-2-(4-hydroxy\nphenyl) thiozolidin-4-one (5A-J), which was prepared by using microwave irradiation. The\nstructures of all newly synthesized motifs were characterized by spectral analysis (IR, 1H NMR, 13C\nNMR spectroscopy) and screened for antibacterial activity against Escherichia coli, Pseudomonas\naeruginosa, Staphylococcus aureus and Streptococcus pyogenes; antifungal activity against Candida\nalbicans, Aspergillus niger, Aspergillus Clavatus; anti-tuberculosis activity against M. tuberculosis\nH37RV and antimalarial activity against Plasmodium falciparum.\n\n\n\nHigher yield with less time-consuming method is the main advantage of Thiazolidin-\n4-one bearing pyrimidine motifs synthesis. The excellent biological response of compounds 5B,\n5C, 5D, 5G, 5H, 5I, and 5J was observed.\n\n\n\nAs compared to conventional method, less time is required for the preparation of Thiazolidin-\n4-one analogues by using advantageous microwave irradiation method. Thiazolidin-4-one\nderivatives showed improved biological activity.\n","PeriodicalId":43539,"journal":{"name":"Current Microwave Chemistry","volume":null,"pages":null},"PeriodicalIF":0.9000,"publicationDate":"2020-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Microwave Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/2213335607999200918155613","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 1
Abstract
To synthesise biologically active thiazolidin-4-one by microwave irradiation
method and evaluate against different species of bacteria, fungi and Plasmodium falciparum.
Microwave irradiation method is serviceable for rapid and sustainable synthesis. In
this present study, Thiazolidin-4-one bearing pyrimidine derivatives have been synthesized by microwave
irradiation method.
Thiazolidin-4-one is a valuable motif because of its broad-spectrum biological evaluation.
It is famous for many types of biological profiles, mainly antimicrobial, anti-tuberculosis, anti-
convulsant, antihypertensive, hypoglycemic agent and antimalarial. This biological response
leads our attention towards the change of Thiazolidin-4-one skeleton to enhance potential. Present
study aims to carry out a rapid synthesis of Thiazolidin-4-one derivative of pyrimidine by microwave-
assisted heating.
4-(4-substituted phenyl)-6-(substituted aryl) pyrimidin-2-amine was the key intermediate
required for the synthesis of 3-(4-(Substituted phenyl)-6-(substituted aryl) pyrimidin-2-yl)-2-(4-hydroxy
phenyl) thiozolidin-4-one (5A-J), which was prepared by using microwave irradiation. The
structures of all newly synthesized motifs were characterized by spectral analysis (IR, 1H NMR, 13C
NMR spectroscopy) and screened for antibacterial activity against Escherichia coli, Pseudomonas
aeruginosa, Staphylococcus aureus and Streptococcus pyogenes; antifungal activity against Candida
albicans, Aspergillus niger, Aspergillus Clavatus; anti-tuberculosis activity against M. tuberculosis
H37RV and antimalarial activity against Plasmodium falciparum.
Higher yield with less time-consuming method is the main advantage of Thiazolidin-
4-one bearing pyrimidine motifs synthesis. The excellent biological response of compounds 5B,
5C, 5D, 5G, 5H, 5I, and 5J was observed.
As compared to conventional method, less time is required for the preparation of Thiazolidin-
4-one analogues by using advantageous microwave irradiation method. Thiazolidin-4-one
derivatives showed improved biological activity.