z-logo
Premium
Studies on condensed heterocyclic compounds II. Synthesis and antibacterial activity of 3‐(4′‐pyridyl)‐6‐aroylamino/arylamino‐ S ‐triazolo[3,4‐ b ]‐1,3,4‐thiadiazoles
Author(s) -
Zhang ZiYi,
Chen Xin
Publication year - 1992
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.19920100111
Subject(s) - chemistry , thiadiazoles , triethylamine , isothiocyanate , antibacterial activity , yield (engineering) , triazole , phenyl isothiocyanate , medicinal chemistry , stereochemistry , organic chemistry , bacteria , materials science , biology , metallurgy , genetics
3‐(4′‐Pyridyl)‐4‐amino‐5‐mercapto‐1,2,4‐triazole (1) reacted with aroyl isothiocyanates 2a‐1 to yield twelve novel 3‐(4′‐pyridyl)‐6‐aroylamino‐ S ‐triazolo [3,4‐ b ]‐1,3,4‐thiadiazoles, 4a‐1 . Triethylamine was necessary for the condensation of 1 with phenyl isothiocyanate ( 3 ) to give 3‐(4′‐ pyridyl)‐6‐phenylamino‐ S ‐triazolo [3,4‐ b ]‐1,3,4‐thiadiazole ( 6 ). The structures were confirmed by the elemental and spectral analyses. Their antibacterial activity against B . Subtilis, E. Coli, E. aerogenes and S. aureus was observed preliminary.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom