Novel chromeno [2,3-b]-pyrimidine derivatives as potential anti-microbial agents

An efficient, microwave irradiated synthesis of novel chromeno[2,3-b]-pyrimidine derivatives was carried out. 2-Amino-3,4-dihydro-2H-chromene-3-carbonitrile was converted into imine using N,N-Dimethylacetaldehyde dimethylacetal to give the core intermediate, which was used for the preparation of chromenopyrimidine library, using acetic acid and different amine in microwave irradiation for 5 min. Structures of newly synthesized compounds were confirmed by spectral studies. Compound 6g was characterized by single crystal X-ray analysis. All the compounds were also screened for their anti-microbial activity. Few of the compounds are found to be potential antimicrobials.

Graphical abstractHeterocyclic privileged medicinal scaffolds involving chromeno[2,3-b]-pyrimidine frameworks are prepared by microwave irradiation.Figure optionsDownload full-size imageDownload as PowerPoint slide