Literature DB >> 22345825

Construction of pyrazolo[3,4-b]pyridines and pyrazolo[4,3-c]pyridines by ring closure of 3-acylpyridine N-oxide tosylhydrazones.

William J Lominac1, Megan L D'Angelo, Mark D Smith, Darius A Ollison, James M Hanna.   

Abstract

3-Acylpyridine N-oxide tosylhydrazones give good overall yields of a mixture of pyrazolo[3,4-b]pyridines and pyrazolo[4,3-c]pyridines when treated with an electrophilic additive and an amine base. (Z)-Hydrazones cyclize readily, while (E)-hydrazones fail to react under the reported conditions. The reaction takes place at room temperature, and moderate regiocontrol over the cyclization can be achieved by varying the electrophile/solvent combination.

Entities:  

Year:  2012        PMID: 22345825      PMCID: PMC3278155          DOI: 10.1016/j.tetlet.2011.12.055

Source DB:  PubMed          Journal:  Tetrahedron Lett        ISSN: 0040-4039            Impact factor:   2.415


  16 in total

1.  5-aryl-pyrazolo[3,4-b]pyridines: potent inhibitors of glycogen synthase kinase-3 (GSK-3).

Authors:  Jason Witherington; Vincent Bordas; Stephen L Garland; Deirdre M B Hickey; Robert J Ife; John Liddle; Martin Saunders; David G Smith; Robert W Ward
Journal:  Bioorg Med Chem Lett       Date:  2003-05-05       Impact factor: 2.823

2.  One-step conversion of azine N-oxides to alpha-1,2,4-triazolo-, 1,2,3-triazolo, imidazolo-, and pyrazoloheteroarenes.

Authors:  John M Keith
Journal:  J Org Chem       Date:  2010-04-16       Impact factor: 4.354

3.  Synthesis and 3D QSAR of new pyrazolo[3,4-b]pyridines: potent and selective inhibitors of A1 adenosine receptors.

Authors:  Fabrizio Manetti; Silvia Schenone; Francesco Bondavalli; Chiara Brullo; Olga Bruno; Angelo Ranise; Luisa Mosti; Giulia Menozzi; Paola Fossa; Maria Letizia Trincavelli; Claudia Martini; Adriano Martinelli; Cristina Tintori; Maurizio Botta
Journal:  J Med Chem       Date:  2005-11-17       Impact factor: 7.446

4.  Regioselective synthesis of 1-alkyl- or 1-aryl-1H-indazoles via copper-catalyzed cyclizations of 2-haloarylcarbonylic compounds.

Authors:  Dolores Viña; Esther del Olmo; José L López-Pérez; Arturo San Feliciano
Journal:  Org Lett       Date:  2007-02-01       Impact factor: 6.005

5.  General and mild preparation of 2-aminopyridines.

Authors:  Allyn T Londregan; Sandra Jennings; Liuqing Wei
Journal:  Org Lett       Date:  2010-10-19       Impact factor: 6.005

6.  Synthesis, antimicrobial activity and conformational analysis of novel substituted pyridines: BF(3)-promoted reaction of hydrazine with 2-alkoxy pyridines.

Authors:  Fatma E Goda; Alaa A-M Abdel-Aziz; Omer A Attef
Journal:  Bioorg Med Chem       Date:  2004-04-15       Impact factor: 3.641

7.  6-heteroaryl-pyrazolo[3,4-b]pyridines: potent and selective inhibitors of glycogen synthase kinase-3 (GSK-3).

Authors:  Jason Witherington; Vincent Bordas; Alessandra Gaiba; Antoinette Naylor; Anthony D Rawlings; Brian P Slingsby; David G Smith; Andrew K Takle; Robert W Ward
Journal:  Bioorg Med Chem Lett       Date:  2003-09-15       Impact factor: 2.823

8.  One step conversion of heteroaromatic-N-oxides to imidazolo-heteroarenes.

Authors:  John M Keith
Journal:  J Org Chem       Date:  2007-12-08       Impact factor: 4.354

9.  Design, synthesis, and biological evaluation of AT1 angiotensin II receptor antagonists based on the pyrazolo[3,4-b]pyridine and related heteroaromatic bicyclic systems.

Authors:  Andrea Cappelli; Chiara Nannicini; Andrea Gallelli; Germano Giuliani; Salvatore Valenti; Gal la Pericot Mohr; Maurizio Anzini; Laura Mennuni; Flora Ferrari; Gianfranco Caselli; Antonio Giordani; Walter Peris; Francesco Makovec; Gianluca Giorgi; Salvatore Vomero
Journal:  J Med Chem       Date:  2008-03-05       Impact factor: 7.446

10.  A general and efficient 2-amination of pyridines and quinolines.

Authors:  Jingjun Yin; Bangping Xiang; Mark A Huffman; Conrad E Raab; Ian W Davies
Journal:  J Org Chem       Date:  2007-05-15       Impact factor: 4.354

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  1 in total

1.  Synthesis of trifluoromethyl-substituted pyrazolo[4,3-c]pyridines - sequential versus multicomponent reaction approach.

Authors:  Barbara Palka; Angela Di Capua; Maurizio Anzini; Gyté Vilkauskaité; Algirdas Sačkus; Wolfgang Holzer
Journal:  Beilstein J Org Chem       Date:  2014-07-31       Impact factor: 2.883

  1 in total

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