New Tricyclic Aryl Quinazoline Derivatives by Suzuki‐Miyaura Cross‐Coupling
A number of new deoxyvasicinone (2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one) and mackinazolinone (6,7,8,9-tetrahydro-11H-pyrido[2,1-b]quinazolin-11-one) derivatives with aryl substituents at C7/C8 and at C5 are reported. These compounds are rare representatives of their kind and were prepared in high yields by Suzuki-Miyaura cross-coupling reactions between 7-bromo-2,3-dihydro[2,1-b]quinazoline-9-(1H)-one, 5,7-dibromo-2,3-dihydro[2,1-b]quinazoline-9-(1H)-one or 8-bromomackinazolinone and respective arylboronic acids with palladium acetate as the catalyst. The products were characterized spectroscopically and, in addition, by X-ray crystal structure analyses in six cases.
Authors
- R. Ya. Okmanov (ORCID: https://orcid.org/0000-0003-2154-0746)
- Burkhon Elmuradov (ORCID: https://orcid.org/0000-0002-9372-8249)
- Bakhromjon B. Juraev (ORCID: https://orcid.org/0000-0002-5382-8894)
- Gerald Dräger (ORCID: https://orcid.org/0000-0003-1988-0469)
- Holger Butenschön (ORCID: https://orcid.org/0000-0002-7689-1992)
Institutions
- Leibniz University Hannover (DE)
- Yunusov Institute of the Chemistry of Plant Substances (UZ)
Publication Details
- Journal
- ChemistryOpen
- Published
- 2024-09-27
- DOI
- https://doi.org/10.1002/open.202400197
- Citations
- 2
- Primary Topic
- Quinazolinone synthesis and applications
- Type
- article
- Field-Weighted Citation Impact
- 0.50
Funders
- Alexander von Humboldt-Stiftung
- Deutscher Akademischer Austauschdienst