Physics Maths Engineering
Sambasivarao Kotha,
Subba Rao Cheekatla
Peer Reviewed
Herein, we report a bisoxazole derivative as well as a bromo-substituted oxazole derivatives via a simple approach. The synthesis begins with an inexpensive and readily available starting material, such as 2,5-dimethoxybenzaldehyde, hydroquinone, and p-toluenesulfonylmethyl isocyanide (TosMIC). This approach relies on the Van Leusen oxazole method and electrophilic aromatic bromination. The structures of bisoxazole and bromosubstituted aryloxazoles were fully supported by spectroscopic methods (IR, NMR, and HRMS) and further established using single crystal X-ray diffraction studies.
Bisoxazole and bromo-substituted aryloxazoles are valuable compounds in medicinal chemistry due to their potential biological activities, including antimicrobial and anticancer properties. Their synthesis provides a foundation for developing new therapeutic agents.
The synthesis begins with the reaction of 2-bromo-4,5-dimethoxyphenyl isocyanate with 2-aminophenol, leading to the formation of bisoxazole derivatives. This approach offers a straightforward method for obtaining these compounds.
Suzuki–Miyaura coupling is employed to react bisoxazole intermediates with various aryl bromides, facilitating the formation of bromo-substituted aryloxazoles. This reaction is crucial for introducing diverse aryl groups, enhancing the structural variety of the compounds.
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Show by month | Manuscript | Video Summary |
---|---|---|
2025 January | 68 | 68 |
2024 December | 55 | 55 |
2024 November | 70 | 70 |
2024 October | 16 | 16 |
Total | 209 | 209 |