A novel approach toward the synthesis of some new tridentate Schiff bases from anil-like compounds
Author(s) -
Fatemeh Bagheri,
Abolfazl Olyaei
Publication year - 2016
Publication title -
journal of the serbian chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.227
H-Index - 45
eISSN - 1820-7421
pISSN - 0352-5139
DOI - 10.2298/jsc151202064b
Subject(s) - imidazopyridine , chemistry , schiff base , catalysis , formic acid , combinatorial chemistry , pyridine , ligand (biochemistry) , condensation , solvent , condensation reaction , organic chemistry , medicinal chemistry , polymer chemistry , biochemistry , physics , receptor , thermodynamics
A novel method was developed for synthesizing a series of new three dentate Schiff base ligands starting from hydroxynaphthalidene pyrimidinyl amines with o-phenylenediamines or o-aminophenol or 2-amino-3-hydroxy-pyri-dine in the presence of formic acid catalyst under solvent-free conditions. In these reactions [1+1] condensation product as half-unit ligand was obtained. Moreover, the reaction of hydroxynaphthalidene pyrimidinyl amines with 3,4-diamino-pyridine and 1,8-naphthalenediamine lead to the formation of C2-naphthylated imidazopyridine and dihydropyrimidine, respectively. The attractive features of this protocol are: use of inexpensive catalyst, operationally simple, short reaction times, easy handling, and good yields
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