Efficient Synthesis of New Pyrimido[5′,4′:5,6]pyrano[2,3-d]pyrimidine-2,4,6(1H,3H)-triones via the Tandem Intramolecular Pinner–Dimroth Rearrangement, and Their Antibacterial Activity View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2018-12

AUTHORS

M. Asadian, A. Davoodnia, S. A. Beyramabadi

ABSTRACT

Synthesis of new 8-alkyl-5-aryl-1,3-dimethyl-5,7-dihydro-2H-pyrimido[5′,4′:5,6]pyrano[2,3-d]- pyrimidine-2,4,6(1H,3H)-triones by the high yield reaction of 7-amino-5-aryl-1,3-dimethyl-2,4-dioxo-1,3,4,5- tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carbonitriles with aliphatic carboxylic acids in the presence of POCl3 is presented. It is probable that synthesis of these new products proceeds via the tandem intramolecular Pinner–Dimroth rearrangement. The products are characterized by FT-IR, 1H, and 13C NMR spectra and evaluated for their antibacterial activity against gram +ve bacteria (Staphylococcus aureus and Staphylococcus epidermidis) and gram–ve bacteria (Escherichia coli and Pseudomonas aeruginosa) using the disc diffusion method. More... »

PAGES

2658-2663

References to SciGraph publications

  • 2013-05. 7-Deazaadenines: synthesis of some new pyrrolo[2,3-d]pyrimidin-4-amines in MONATSHEFTE FÜR CHEMIE - CHEMICAL MONTHLY
  • 2017-10. Synthesis of some new heterocycles containing quinazoline moiety in RUSSIAN JOURNAL OF GENERAL CHEMISTRY
  • 2008-08. Synthesis of pyrido[3′,2′:4,5]thieno[2,3-e][1,2,4]triazolo[4,3-a]pyrimidin-5(4H)-one derivatives in MONATSHEFTE FÜR CHEMIE - CHEMICAL MONTHLY
  • 2018-01. Synthesis of functionalized triazolo[1,5-a]pyrimidine derivatives in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2016-11. Synthesis, biological screening and molecular docking studies of novel 4,6-pyrimidine derivatives as EGFR-TK inhibitors in MEDICINAL CHEMISTRY RESEARCH
  • 2017-10. Design, synthesis, and evaluation of novel hydrazide hydrochlorides of 6-aminopyrazolo[1,5-a]pyrimidine-3-carboxamides as potent Aurora kinase inhibitors in MONATSHEFTE FÜR CHEMIE - CHEMICAL MONTHLY
  • 2017-12. Synthesis of New Functionalized 1,4-Dihydroquinolines and Pyrimido[4,5-b]quinolines in RUSSIAN JOURNAL OF GENERAL CHEMISTRY
  • 2015-09. Synthesis, characterization, and antibacterial evaluation of new alkyl 2-amino-4-aryl-4H-chromene-3-carboxylates in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2007-04. Azines and azoles: CXXVII. Glycosylation of 5,7-dihydro-4H-pyrano-[2,3-d:6,5-d′]dipyrimidine-4,6(3H)-dione and its 5-phenyl-substituted analog in RUSSIAN JOURNAL OF GENERAL CHEMISTRY
  • 2017-04. Efficient one-pot synthesis of some new pyrimido[5′,4′:5,6]pyrido[2,3-d]pyrimidines catalyzed by magnetically recyclable Fe3O4 nanoparticles in RUSSIAN JOURNAL OF GENERAL CHEMISTRY
  • 2017-04. Synthesis and antibacterial activity of novel pyrano[2,3-d]pyrimidine-4-one–3-phenylisoxazole hybrids in RUSSIAN JOURNAL OF GENERAL CHEMISTRY
  • Identifiers

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    http://scigraph.springernature.com/pub.10.1134/s1070363218120290

    DOI

    http://dx.doi.org/10.1134/s1070363218120290

    DIMENSIONS

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