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 language | English |
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Pages (from-to) | 33-41 |
Number of pages | 9 |
Journal | Journal of combinatorial chemistry |
Volume | 7 |
Issue number | 1 |
DOIs | |
Publication status | Published - 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