SYNTHESIS OF 1, 3, 4-OXADIZAOLE INCORPORATED THIOFIBRATES FROM SUBSTITUTED BENZOIC ACIDS
Niranjan M. S.* and Chaluvaraju K. C.
ABSTRACT
The present discussion describes about five derivatives 5a to 5e of 1, 3,
4-oxadizaole incorporated thiofibrates. These were synthesized from
the starting material substituted benzoic acids 1a to 1e. Methyl esters
2a to 2e of these acids are converted into their hydrazides 3a to 3e by
refluxing with hydrazine hydrate. Further reaction with carbon
disulphide in 10% potassium hydroxide gives corresponding
thiophenols incorporated with 1, 3, 4-oxadizole 4a to 4e. Ethyl-2-
bromoisobutyrate in dimethylformamide converts these into their
thiofibrates 5a to 5e in presence of anhydrous potassium carbonate.
Physical data such as m. p, TLC and spectral data IR, NMR, Mass
confirms their assigned structures.
Keywords: 1, 3, 4-oxadizole, thio fibrates, Ethyl-2-bromoisobutyrate, synthesis, hypolipidemia.
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