Abstract3-(5-(2-oxido)-(4-substitudedphenoxy)-benzo[
d][1,3,2]dioxaphosphol-5-yl)-1
H-tetrazol-1-yl)thiophene-2-carboxamides(9a-g) were synthesized by condensing 3-(5-(3,4-dihydroxyphenyl)-1
H-tetrazol-1-yl)thiophene-2-carboxamide
(7) with 4-substituted phenyl phosphoro dichloridates (8a-g).
The synthon (7) was synthesized by hydrolysis of 3-(5-(3,4-dimethoxyphenyl)-1
H-tetrazol-1-yl)thiophene-2-carboxamide (6).
The intermediate (6) was synthesized by condensing 3-((3,4-dimethoxy benzylidine)amino)thiophene-2-carboxamide (5) with
sodium azide in Tetrahydrofuron.
The synthon (5) was synthesized by reaction between 3-aminothiophene-2-caroxamide (3) and 3,4-dimethoxybenzaldehyde (4).
Starting intermediate (3) was synthesized by condensation reaction between 2-cyano acetamide (1) and 1,4-dithiane-2,5-diol (2).
The reagents and conditions were shown in a, b, c, d and e.
The synthetic route was shown in Scheme-I.
The target molecules (9a-g) were characterized by IR, 1HNMR, 13C-NMR, Mass and elemental analysis. The target molecules were subjected to biological evaluation and molecular docking studies. The results observed in the present investigation were reported in this present research article.