“…Multi-component reactions (MCRs) play an important role in combinatorial chemistry [1]. This method has the capability for producing desired small molecule drugs with various degrees of structural diversity [2]. When three or more than three substances or reactants are reacted simultaneously to produce defined target molecules these reactions are said to be MCRs.…”
This study deals with a new and efficient metal-free regioselective synthesis of pyrimido-fused indazoles with nitrogen ring junction motifs. We have developed a metal-free domino type reaction between 3-aminoindazole, aryl aldehydes and aceotophenones in the presence of KOH/DMF that leads to pyrimido[1,2-b]indazole analogues. Response Surface Methodology (RSM) coupled with a Box-Behnken design (BBD) were utilized for exploring the effect of base used (A), temperature of reaction (B) and (C), reaction time. This approach can allow access to a variety of pyrimidoindazole fluorophores and related compounds. The compound N,N-dimethyl-4-(2-phenylpyrimido[1,2-b]indazol-4-yl)aniline (4e) displays the maximum fluorescence intensity at 518 nm and shows a fluorescence quantum yield of 0.068. The synthesized pyramido-fused indazoles have been evaluated for their free radical scavenging activity and compound 4f showed good antioxidant activity.
“…Multi-component reactions (MCRs) play an important role in combinatorial chemistry [1]. This method has the capability for producing desired small molecule drugs with various degrees of structural diversity [2]. When three or more than three substances or reactants are reacted simultaneously to produce defined target molecules these reactions are said to be MCRs.…”
This study deals with a new and efficient metal-free regioselective synthesis of pyrimido-fused indazoles with nitrogen ring junction motifs. We have developed a metal-free domino type reaction between 3-aminoindazole, aryl aldehydes and aceotophenones in the presence of KOH/DMF that leads to pyrimido[1,2-b]indazole analogues. Response Surface Methodology (RSM) coupled with a Box-Behnken design (BBD) were utilized for exploring the effect of base used (A), temperature of reaction (B) and (C), reaction time. This approach can allow access to a variety of pyrimidoindazole fluorophores and related compounds. The compound N,N-dimethyl-4-(2-phenylpyrimido[1,2-b]indazol-4-yl)aniline (4e) displays the maximum fluorescence intensity at 518 nm and shows a fluorescence quantum yield of 0.068. The synthesized pyramido-fused indazoles have been evaluated for their free radical scavenging activity and compound 4f showed good antioxidant activity.
“…The known compounds were characterized by comparing the obtained data with their authentic reports. 64 The spectral data of the new derivatives (6e and 6f) are presented in the Experimental section. Furthermore, to extend the efficacy of the novel nano Fe 3Àx Bi x O 4 /SiO 2 @L-ArgEt 3 + I À /Zn(II) the preparation of malonamides 7a-f through a pseudo six-component condensation was performed successfully under the optimal reaction conditions within 10-19 h in 65-98% yield Table 5 (method A).…”
Section: Characterization Of the Bionanocompositementioning
In this work, a new magnetized composite of bismuth (Fe3−xBixO4) was prepared and functionalized stepwise with silica, triethylargininium iodide ionic liquid, and Zn(ii) to prepare a multi-layered core–shell bio-nanostructure, [Fe3−xBixO4/SiO2@l-ArgEt3+I−/Zn(ii)].
“…Benzo[b] [1,4]diazepines are important nitrogen-containing heterocyclic compounds, which have extensive applications in synthetic chemistry [4][5][6] and medicinal chemistry [7][8][9][10]. The crystal structure of title compound is shown in the figure.…”
Section: Commentmentioning
confidence: 99%
“…The bond lengths and angles in the title molecule are in the normal ranges. In conclusion, an efficient and novel one-pot multi-component approach to the synthesis of benzo[b] [1,4]diazepines from simple and readily available starting materials under refluxing conditions without modifications has been developed. We hope that this approach may be of value to others seeking novel synthetic fragments for medicinal chemistry.…”
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