Premium
A Facile Synthesis of Aryl‐Substituted Hydrazono‐Pyrazolyl[1,2,4]triazolo[3,4‐ b ][1,3,4][thiadiazol]‐coumarin Derivatives
Author(s) -
Sharma Archi,
Satish Gudala,
Penta Santhosh
Publication year - 2016
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.2362
Subject(s) - chemistry , coumarin , aryl , proton nmr , 1,2,4 triazole , condensation reaction , medicinal chemistry , organic chemistry , catalysis , alkyl
Some inimitable and therapeutic coumarin‐substituted fused[1,2,4]triazolo‐[3,4‐ b ][1,3,4]thiadizole derivatives were synthesized by the cyclocondensation reaction of 2‐oxo‐2 H ‐chromene‐3‐carboxylic acid ( 1 ) and 4‐amino‐5‐hydrazinyl‐4 H ‐[1,2,4]‐triazole‐3‐thiol ( 2 ) by using phosphorous oxychloride as a cyclizing agent. This cyclized intermediate 3‐(3‐hydrazino‐[1,2,4]triazolo[3,4‐ b ][1,3,4]thiadiazol‐6‐yl)‐chromen‐2‐one ( 3 ) later condensation with various ethyl 2‐(2‐arylhydrazono)‐3‐oxobutanoates ( 4 ) in NaOAc/MeOH under reflux conditions afforded the corresponding new series of aryl‐substituted hydrazono‐pyrazolyl‐[1,2,4]triazolo[3,4‐ b ][1,3,4][thiadiazol]‐coumarin derivatives ( 5 ) in good to excellent yields. The structures of newly synthesized compounds were established on the basis of elemental analysis, IR, 1 H NMR and mass spectroscopic studies.