Unknown

Dataset Information

0

Iodine-Catalyzed Multicomponent Synthesis of Highly Fluorescent Pyrimidine-Linked Imidazopyridines.


ABSTRACT: Herein, we report a metal-free one-pot three-component reaction of aryl methyl ketones, 2-aminopyridines, and barbituric acids for the synthesis of pyrimidine-linked imidazopyridines using a catalytic amount of molecular iodine in DMSO medium. This process involves a one-pot C-H oxidation, followed by the formation of one C-C and two C-N bonds. A wide variety of aryl methyl ketones and 2-aminopyridines were found to be suitable for this methodology. The UV and fluorescence properties of the synthesized products were studied in water and DMSO media. Most of the synthesized products exhibited very good to excellent fluorescence quantum yield. Among all the products, compounds 4p and 4q showed the maximum fluorescence quantum yield (0.36) in water medium under basic conditions and compound 4c showed the maximum fluorescence quantum yield (0.75) in DMSO medium.

SUBMITTER: Acharya SS 

PROVIDER: S-EPMC9178772 | biostudies-literature | 2022 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications

Iodine-Catalyzed Multicomponent Synthesis of Highly Fluorescent Pyrimidine-Linked Imidazopyridines.

Acharya Swadhin Swaraj SS   Bhaumick Prabhas P   Kumar Rohit R   Choudhury Lokman H LH  

ACS omega 20220525 22


Herein, we report a metal-free one-pot three-component reaction of aryl methyl ketones, 2-aminopyridines, and barbituric acids for the synthesis of pyrimidine-linked imidazopyridines using a catalytic amount of molecular iodine in DMSO medium. This process involves a one-pot C-H oxidation, followed by the formation of one C-C and two C-N bonds. A wide variety of aryl methyl ketones and 2-aminopyridines were found to be suitable for this methodology. The UV and fluorescence properties of the synt  ...[more]

Similar Datasets

| S-EPMC6244180 | biostudies-literature
| S-EPMC6719937 | biostudies-literature
| S-EPMC10766964 | biostudies-literature
| S-EPMC2517582 | biostudies-literature
| S-EPMC7525493 | biostudies-literature
| S-EPMC3517165 | biostudies-literature
| S-EPMC9273986 | biostudies-literature
| S-EPMC7372561 | biostudies-literature
| S-EPMC5263222 | biostudies-literature
| S-EPMC9055358 | biostudies-literature