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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-...

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Detalles Bibliográficos
Autores principales: Sepehrmansourie, Hassan, Kalhor, Sima, Zarei, Mahmoud, Zolfigol, Mohammad Ali, Hosseinifard, Mojtaba
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
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
Descripción
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.