Title:Chemistry of 2-Aminoquinolines: Synthesis, Reactivity, and Biological
Activities
Volume: 20
Issue: 5
Author(s): Moustafa A. Gouda*Ghada G. El-Bana*
Affiliation:
- Department of Chemistry, Faculty of Science and Arts, Taibah University, Ulla, Medina, Saudi Arabia
- Department of
Chemistry, Faculty of Science, Mansoura University, El-Gomhoria Street, Mansoura 35516, Egypt
- Department of
Chemistry, Faculty of Science, Mansoura University, El-Gomhoria Street, Mansoura 35516, Egypt
- Mansoura
University Student Hospital, Mansoura University, El-Gomhoria Street, Mansoura ET- 35516, Egypt
Keywords:
2-chloroquinoline-3-carbaldehyde, 2-aminoquinoline-3-carbaldehydes, Vilsmeier-Haack, synthesis, reactivity, reductive animation.
Abstract: This review described the preparation of 2-chloroquinoline-3-carbaldehyde derivatives
through Vilsmeier-Haack formylation of N-arylacetamides and their use as a key intermediate for the
preparation of 2-aminoquinoline-3-carbaldehydes. The synthesis of the 2-aminoquinolines can be done
through the following chemical reactions: Claisen-Schmidt condensation, 1, 3-dipolar cycloaddition,
one-pot multicomponent reactions (MCRs), and reductive amination.