60467-64-3Relevant articles and documents
An Exceedingly Mild, Green Synthesis of Substituted N-3-diaryl-1,8-naphthyridin-2-amine Derivatives and Their Antimicrobial Activity
Ravi, Dharavath,Rambabu, Sirgamalla,Ashok, Kommakula,Madhu, Palithapu,Sakram, Boda
, p. 957 - 963 (2018/02/26)
An exceedingly and highly efficient procedure has been described for the synthesis of substituted N-3-diaryl-1,8-naphthyridin-2-amines by the reaction of 2-chloro-3-aryl-1,8-naphthyridines with various anilines in the presence of N-methyl-2-pyrrolidone and K2CO3 under thermal green solvent-free conditions. The significant features of this green reaction include very good yields in purity, simple experimental, short reaction time, easy workability, and avoidance of toxic solvents. All synthesized compounds have been evaluated for their antibacterial activity.
An exceedingly mild and efficient synthesis of 1,2,4-Triazolo[4,3-α][1,8]naphthyridines using iodobenzene diacetate in the solid state
Mogilaiah,Babu, H. Ramesh,Reddy, N. Vasudeva
, p. 2377 - 2384 (2007/10/03)
An efficient and mild method for the synthesis of 1,2,4-triazolo[4,3-α][1,8]naphthyridines using iodobenzene diacetate (IBD) in the solid state at room temperature has been described. The reaction proceeds efficiently at room temperature in good yields and in a solid of high purity.
