Facile Catalyst-Free Synthesis of New Functionalized 1H-Pyrazolo[1,2-b]phthalazines View Full Text


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Article Info

DATE

2018-12

AUTHORS

M. Elmi-Mehr, A. Davoodnia, M. Pordel

ABSTRACT

Some new derivatives of 3-amino-1-aryl-N-butyl-5,10-dioxo-5,10-dihydro-1H-pyrazolo[1,2-b]- phthalazine-2-carboxamide are synthesized via in situ Knoevenagel condensation of aromatic aldehydes with N-butyl-2-cyanoacetamide, which leads to 3-aryl-N-butyl-2-cyanoacrylamides. This is followed by the reaction with phthalhydrazide upon refluxing in ethanol under catalyst-free conditions. The products are characterized on the basis of IR, 1H and 13C NMR spectral data. More... »

PAGES

2595-2600

References to SciGraph publications

  • 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
  • 2018-03. A convenient approach for the synthesis of various derivatives of pyrazolo[1,2-b]phthalazinediones in the presence of an efficient supported basic ionic liquid at ambient temperature and solvent-free media in JOURNAL OF THE IRANIAN CHEMICAL SOCIETY
  • 2002-11. Synthesis and Pharmacological Activity of 1-Hydroxy-, 1-Amino-, and 1-Hydrazino-Substituted 2,3-Dihydro-1H-pyrazolo[1,2-a]pyridazine-5,8-diones and 2,3-Dihydro-1H-pyrazolo[1,2-b]phthalazine-5,10-diones in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 2017-10. Preparation, characterization, and first catalytic application of a novel phosphotungstic acid-containing ionic liquid immobilized on CuFe2O4@SiO2 magnetic nanoparticles in the synthesis of 1H-pyrazolo[1,2-b]phthalazine-5,10-diones in RUSSIAN JOURNAL OF GENERAL CHEMISTRY
  • 2013-04. Nano-ZnO: an efficient and reusable catalyst for one-pot synthesis of 1H-pyrazolo[1,2-b]phthalazine-5,10-diones and pyrazolo[1,2-a][1,2,4]triazole-1,3-diones in JOURNAL OF THE IRANIAN CHEMICAL SOCIETY
  • 2016-03. Synthesis of 1H-pyrazolo[1,2-b]phthalazine-5,10-dione derivatives: assessment of their antimicrobial, antituberculosis and antioxidant activity in RESEARCH ON CHEMICAL INTERMEDIATES
  • 2012-10. Synthesis and evaluation of anti-proliferative activity of 1,4-disubstituted phthalazines in MEDICINAL CHEMISTRY RESEARCH
  • 2016-07. Ultrasound-assisted synthesis of pyrazolo[1,2-b]phthalazines and dihydrospiro[indoline-3,1'-pyrazolo[1,2-b]phthalazines] using TBAF as an efficient phase-transfer catalyst in RUSSIAN JOURNAL OF GENERAL CHEMISTRY
  • 2015-11. Synthesis, characterization, analgesic and anti-inflammation activity of new phthalazines and their Cu(II) and Zn(II) complexes in MEDICINAL CHEMISTRY RESEARCH
  • 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
  • 2017-12. Synthesis of New Functionalized 1,4-Dihydroquinolines and Pyrimido[4,5-b]quinolines in RUSSIAN JOURNAL OF GENERAL CHEMISTRY
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    http://scigraph.springernature.com/pub.10.1134/s1070363218120216

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    http://dx.doi.org/10.1134/s1070363218120216

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