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A convenient catalytic method for preparation of new tetrahydropyrido[2,3-d]pyrimidines via a cooperative vinylogous anomeric based oxidation
In this study, a novel functionalized metal–organic frameworks MIL-125(Ti)-N(CH(2)PO(3)H(2))(2) was designed and synthesized via post-modification methodology. Then, MIL-125(Ti)-N(CH(2)PO(3)H(2))(2) as a mesoporous catalyst was applied for the synthesis of a wide range of novel tetrahydropyrido[2,3-...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9709663/ https://www.ncbi.nlm.nih.gov/pubmed/36545580 http://dx.doi.org/10.1039/d2ra05655k |
Sumario: | In this study, a novel functionalized metal–organic frameworks MIL-125(Ti)-N(CH(2)PO(3)H(2))(2) was designed and synthesized via post-modification methodology. Then, MIL-125(Ti)-N(CH(2)PO(3)H(2))(2) as a mesoporous catalyst was applied for the synthesis of a wide range of novel tetrahydropyrido[2,3-d]pyrimidines as bioactive candidate compounds by one-pot condensation reaction of 3-(1-methyl-1H-pyrrol-2-yl)-3-oxopropanenitrile, 6-amino-1,3-dimethylpyrimidine-2,4(1H,3H)-dione and aromatic aldehydes at 100 °C under solvent-free condition. Interestingly, the preparation of tetrahydropyrido[2,3-d]pyrimidine was achieved via vinylogous anomeric based oxidation mechanism with a high yield and short reaction time. |
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