TY - JOUR
T1 - Synthesis and antibacterial activities of 4-amino-3-(1-aryl-5-methyl-1,2,3- triazol-4-yl)-5-mercapto-1,2,4-triazoles/2-amino-5-(1-aryl-5-methyl-1,2, 3-triazol-4-yl)-1,3,4-thiadiazoles and their derivatives
AU - Zhang, Yan
AU - Sun, Xiao Wen
AU - Hui, Xin Ping
AU - Zhang, Zi Yi
AU - Wang, Qin
AU - Zhang, Qi
N1 - Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2002/2
Y1 - 2002/2
N2 - Treatment of 4-amino-3-(1-aryl-5-methyl-1,2,3-triazol-4-yl)-5-mercapto-1,2, 4-triazoles/2-amino-5-(1-aryl-5-methyl-1,2, 3-triazol-4-yl)-1,3,4-thiadiazoles with benzaldehyde, acetone and ω-bromoacetophenone was tested and compared. The title compounds Schiff bases, amides, imidazolo[2,1-b]-1,3,4- thiadiazoles and 7H-s-triazolo [3,4-b]-1,3,4-thiadiazines have been confirmed by elemental analyses, 1H NMR, IR and MS spectra. All the compounds have also been screened for their antibacterial activities against B. subtilis, S. aureus and E. coli.
AB - Treatment of 4-amino-3-(1-aryl-5-methyl-1,2,3-triazol-4-yl)-5-mercapto-1,2, 4-triazoles/2-amino-5-(1-aryl-5-methyl-1,2, 3-triazol-4-yl)-1,3,4-thiadiazoles with benzaldehyde, acetone and ω-bromoacetophenone was tested and compared. The title compounds Schiff bases, amides, imidazolo[2,1-b]-1,3,4- thiadiazoles and 7H-s-triazolo [3,4-b]-1,3,4-thiadiazines have been confirmed by elemental analyses, 1H NMR, IR and MS spectra. All the compounds have also been screened for their antibacterial activities against B. subtilis, S. aureus and E. coli.
KW - 7H-s-triazolo[3,4-b]- 1,3,4-thiadiazine
KW - Amide
KW - Imidazolo[2,1-b]-1,3,4-thiadiazole
KW - Schiff base
UR - http://www.scopus.com/inward/record.url?scp=2442557821&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=2442557821&partnerID=8YFLogxK
U2 - 10.1002/cjoc.20020200210
DO - 10.1002/cjoc.20020200210
M3 - Article
AN - SCOPUS:2442557821
VL - 20
SP - 168
EP - 173
JO - Chinese Journal of Chemistry
JF - Chinese Journal of Chemistry
SN - 1001-604X
IS - 2
ER -