Literature DB >> 15638476

Multicomponent reactions with dihydroazines: efficient synthesis of a diverse set of pyrido-fused tetrahydroquinolines.

Inés Carranco1, José Luis Díaz, Oscar Jiménez, Marc Vendrell, Fernando Albericio, Miriam Royo, Rodolfo Lavilla.   

Abstract

A multicomponent assembly of pyrido-fused tetrahydroquinolines is accomplished in a one-pot process from the interaction of dihydroazines, aldehydes, and anilines. A rational screening of the different components and parameters of this reaction, such as the range of reactive starting materials, catalysts and reaction conditions (solvent range; thermal, high pressure- and microwave-promoted processes) is carried out. Optimized conditions allow an efficient preparation of pyrido-fused tetrahydroquinolines with good yields, bypassing the biomimetic NADH-like reductive pathway which is typical in the interaction of dihydropyridines with carbonyl compounds and amines. Furthermore, solid-supported versions of the process have been developed, which should facilitate the preparation of libraries.

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Year:  2005        PMID: 15638476     DOI: 10.1021/cc049877a

Source DB:  PubMed          Journal:  J Comb Chem        ISSN: 1520-4766


  2 in total

1.  An interrupted Ugi reaction enables the preparation of substituted indoxyls and aminoindoles.

Authors:  John S Schneekloth; Jimin Kim; Erik J Sorensen
Journal:  Tetrahedron       Date:  2009-04-18       Impact factor: 2.457

2.  Solid-phase synthesis and chemical properties of 2-(2-amino/hydroxyethyl)-1-aryl-3,4-dihydropyrazino[1, 2-b]indazol-2-iums.

Authors:  Jan Kocí; Viktor Krchnák
Journal:  J Comb Chem       Date:  2010 Jan-Feb
  2 in total

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