tetano
Editor, Senior Moderator
ACS Comb Sci. 2017 Jun 5. doi: 10.1021/acscombsci.7b00016. [Epub ahead of print]
[h=1]"On-water" facile synthesis of novel pyrazolo[3,4-b]pyridinones possessing anti-influenza virus activity.[/h] Zeng LY, Liu T, Yang J, Yang Y, Cai C, Liu SW.
[h=3]Abstract[/h] A facile and versatile "on-water" protocol for the synthesis of pyrazolo[3,4-b]pyridinones was developed by the unprecedented construction of two rings and five new bonds in one-pot. It was proved that water was an important promoter of the reaction and PEG2000 was found to improve the reaction in terms of yield. 32 Derivatives were newly synthesized and most of them were prepared in an hour. The scope and limitation indicated that electron withdrawing groups substituted on synthons, substituted benzoyl acetonitriles or aryl aldehydes, were helpful to construct the pyrazolo[3,4-b]pyridinones. The reaction media PEG2000/H2O was successfully recycled and reused at least 5 times without any obvious decrease in yield. The anti-influenza activities of the derivatives were evaluated and the screening results highlighted two derivatives, which exhibited strong inhibitory activity against H5N1 pseudovirus. These positive bioassay results implied that the library of potential anti-influenza virus agents as candidates could be rapidly prepared in an eco-friendly manner, and provided a new insight into drug discovery for medicinal chemists.
PMID: 28581706 DOI: 10.1021/acscombsci.7b00016
[h=1]"On-water" facile synthesis of novel pyrazolo[3,4-b]pyridinones possessing anti-influenza virus activity.[/h] Zeng LY, Liu T, Yang J, Yang Y, Cai C, Liu SW.
[h=3]Abstract[/h] A facile and versatile "on-water" protocol for the synthesis of pyrazolo[3,4-b]pyridinones was developed by the unprecedented construction of two rings and five new bonds in one-pot. It was proved that water was an important promoter of the reaction and PEG2000 was found to improve the reaction in terms of yield. 32 Derivatives were newly synthesized and most of them were prepared in an hour. The scope and limitation indicated that electron withdrawing groups substituted on synthons, substituted benzoyl acetonitriles or aryl aldehydes, were helpful to construct the pyrazolo[3,4-b]pyridinones. The reaction media PEG2000/H2O was successfully recycled and reused at least 5 times without any obvious decrease in yield. The anti-influenza activities of the derivatives were evaluated and the screening results highlighted two derivatives, which exhibited strong inhibitory activity against H5N1 pseudovirus. These positive bioassay results implied that the library of potential anti-influenza virus agents as candidates could be rapidly prepared in an eco-friendly manner, and provided a new insight into drug discovery for medicinal chemists.
PMID: 28581706 DOI: 10.1021/acscombsci.7b00016