Abstract
Aims: This study aimed to employ sustainable green methods in the synthesis of bisfused cycles incorporating pyrido[2,3-d]pyrimidine moiety using a green catalyst nano ZnO catalyst by one-pot, multicomponent reaction among 2,2'-(propane-1,3-diylbis(sulfanediyl)) bis(6-aminopyrimidin-4(3H)-one) 3, 1H-indene-1,3(2H)-dione 4, and aromatic aldehydes 5.
Method: The reactions proceeded with both conventional and microwave (MW) irradiation methods.
Result: The microwave-assisted method carried out the reaction in 10 min and had high yields (89-95%).
Conclusion: A molecular docking simulation study was conducted using human serum albumin (PDB: ID (2XVQ)). The study revealed that compounds strongly fit into the active sites of the target protein.
[http://dx.doi.org/10.2174/9789814998277121010013]
[http://dx.doi.org/10.2174/2213335604666170830122722]
[http://dx.doi.org/10.2174/97898149982771210101]
[http://dx.doi.org/10.1016/j.jtusci.2017.05.005]
[http://dx.doi.org/10.1155/2014/406869]
[http://dx.doi.org/10.1016/j.ejmech.2021.113218] [PMID: 33540357]
[http://dx.doi.org/10.3390/molecules24224161] [PMID: 31744155]
[http://dx.doi.org/10.3923/ijbc.2015.148.177]
[http://dx.doi.org/10.1016/j.ejmech.2014.06.027] [PMID: 24956552]
[http://dx.doi.org/10.1016/j.bmcl.2008.09.057] [PMID: 18842404]
[http://dx.doi.org/10.1016/j.molstruc.2013.09.046]
[http://dx.doi.org/10.1016/j.bmcl.2009.05.044] [PMID: 19481936]
[http://dx.doi.org/10.1016/j.steroids.2012.09.001] [PMID: 22999991]
[http://dx.doi.org/10.1002/jhet.2699]
[http://dx.doi.org/10.1186/s13045-015-0194-5] [PMID: 26264704]
[http://dx.doi.org/10.1002/jcp.25427] [PMID: 27186656]
[http://dx.doi.org/10.1007/s12272-012-1107-6] [PMID: 23212632]
[http://dx.doi.org/10.1021/jm401073p] [PMID: 24417566]
[http://dx.doi.org/10.4155/fmc-2019-0050] [PMID: 31544523]
[http://dx.doi.org/10.1021/jm049355+] [PMID: 15801830]
[http://dx.doi.org/10.1007/978-1-60761-178-3_15]
[http://dx.doi.org/10.1016/j.bmc.2009.10.039] [PMID: 19889545]
[http://dx.doi.org/10.1016/j.ejmech.2021.113273] [PMID: 33601310]
[http://dx.doi.org/10.1080/14756366.2018.1437729] [PMID: 29482389]
[http://dx.doi.org/10.1016/j.bmcl.2012.01.019] [PMID: 22326168]
[http://dx.doi.org/10.1002/jhet.3945]
[PMID: 24362994]
[http://dx.doi.org/10.1016/j.jscs.2014.06.007]
[http://dx.doi.org/10.1039/c3ra23254a]
[http://dx.doi.org/10.1016/j.jscs.2011.10.023]
[http://dx.doi.org/10.1016/j.tet.2012.04.051]
[http://dx.doi.org/10.1016/j.tet.2011.06.051]
[http://dx.doi.org/10.1016/j.cclet.2012.01.001]
[http://dx.doi.org/10.1016/j.cclet.2014.04.025]
[http://dx.doi.org/10.1515/achi-2016-0002]
[http://dx.doi.org/10.1515/cse-2016-0002]
[http://dx.doi.org/10.2174/1570179420666230330081211]
[http://dx.doi.org/10.1177/1747519820988806]
[http://dx.doi.org/10.1002/cjoc.200990192]
[http://dx.doi.org/10.1081/SCC-120030318]
[http://dx.doi.org/10.1016/j.tetlet.2003.09.063]
[http://dx.doi.org/10.1021/ar700238s] [PMID: 18419142]
[http://dx.doi.org/10.1186/s13065-016-0165-0] [PMID: 27127538]
[http://dx.doi.org/10.21608/ejchem.2016.1449]
[http://dx.doi.org/10.1023/A:1011014629551] [PMID: 11451040]
[http://dx.doi.org/10.1016/S0167-4838(99)00098-9] [PMID: 10407153]
[http://dx.doi.org/10.1371/journal.pone.0180404] [PMID: 28662200]
[http://dx.doi.org/10.1016/j.bbrep.2018.05.002] [PMID: 29872747]
[http://dx.doi.org/10.1016/j.jsb.2010.10.004] [PMID: 20940056]
[http://dx.doi.org/10.3390/molecules21081054] [PMID: 27537865]
[http://dx.doi.org/10.23893/1307-2080.APS.05821]
[http://dx.doi.org/10.1039/c3ra45795h]