TY - JOUR
T1 - Synthesis and antibacterial activities of 1,3,4-oxadiazole derivatives containing 5-methylisoxazole moiety
AU - Hui, Xin Ping
AU - Chu, Chang Hu
AU - Zhang, Zi Yi
AU - Wang, Qin
AU - Zhang, Qi
N1 - Copyright:
Copyright 2004 Elsevier Science B.V., Amsterdam. All rights reserved.
PY - 2002/10/1
Y1 - 2002/10/1
N2 - 5-(5-Methylisoxazol-3-yl)-4-substituted aminomethyl-2-thio-1,3,4-oxadiazoles 3a-e and 4-acetyl-2-(5-methylisoxazol-3-yl)-5-substituted-1,3,4-oxadiazoles 5a-c have been synthesized by Mannich reaction of 5-(5-methylisoxazol-3-yl)-1,3,4-oxadiazol-2-thiol 2 with amines and cyclization of hydrazones with acetic anhydride, respectively. Moreover, 2-aryl-5-(5-methylisoxazol-3-yl)-1,3,4-oxadiazoles 6a-c have been obtained by direct condensation of 5-methylisoxazol-3-acetic acid hydrazizide with aromatic acid in the presence of POCl3. The compounds synthesized have been confirmed by their elemental analyses and spectral data. Their antibacterial activities have also been evaluated.
AB - 5-(5-Methylisoxazol-3-yl)-4-substituted aminomethyl-2-thio-1,3,4-oxadiazoles 3a-e and 4-acetyl-2-(5-methylisoxazol-3-yl)-5-substituted-1,3,4-oxadiazoles 5a-c have been synthesized by Mannich reaction of 5-(5-methylisoxazol-3-yl)-1,3,4-oxadiazol-2-thiol 2 with amines and cyclization of hydrazones with acetic anhydride, respectively. Moreover, 2-aryl-5-(5-methylisoxazol-3-yl)-1,3,4-oxadiazoles 6a-c have been obtained by direct condensation of 5-methylisoxazol-3-acetic acid hydrazizide with aromatic acid in the presence of POCl3. The compounds synthesized have been confirmed by their elemental analyses and spectral data. Their antibacterial activities have also been evaluated.
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M3 - Article
AN - SCOPUS:0036815785
SN - 0376-4699
VL - 41
SP - 2176
EP - 2179
JO - Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry
JF - Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry
IS - 10
ER -