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

[No Value] Carranco, JL Diaz, O Jimenez, M Vendrell, F Albericio, M Royo, R Lavilla*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish
Pages (from-to)33-41
Number of pages9
JournalJournal of combinatorial chemistry
Volume7
Issue number1
DOIs
Publication statusPublished - 2005

Keywords

  • DIELS-ALDER REACTION
  • SOLID-PHASE SYNTHESIS
  • ONE-POT SYNTHESIS
  • ALPHA-AMINO-ACID
  • N-ARYL IMINES
  • LEWIS-ACID
  • QUINOLINE DERIVATIVES
  • MEDICINAL CHEMISTRY
  • ORIENTED SYNTHESIS
  • DRUG DISCOVERY

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