<?xml version="1.0" encoding="utf-8"?>
<Journal>
<Journal-Info>
<name>International Journal of Pharma and Bio Sciences</name>
<website>ijpbs.net</website>
<email>editorijpbs@rediffmail.com (or) editorofijpbs@yahoo.com (or) prasmol@rediffmail.com</email>
</Journal-Info>
<article>
<article-id pub-id-type='other'>10.22376/ijpbs.2019.10.1.p1-12</article-id>
<issue_number>Volume 1 Issue 3</issue_number>
<issue_period>2010 (July - September) </issue_period>
<title>Synthesis, Characterization and Anthelmintic Activity (Perituma Posthuma) of New Oxadiazole Incorporated with Imidazole and Pyrazole</title>
<abstract>Various substituted 3-amino-1-(2,4-dinitro phenyl)-5-[(5-substituted-1,3,4-oxadiazol-2-yl)amino]-1-Hpyrazole-4-carboxyamide and (5E)-5-[4-(dimethylamino) benzylidene]-3-(5-substituted-1,3,4oxadiazol-2-yl)-2-phenyl-3,5-di hydro-4H-imidazol-4-one containing different functional groups have been synthesised by using different aromatic aldehydes and semicarbazide. Different aldehydes and semicarbazide react to form semicarbazone. This was reacted with I2/KI solution to get corresponding 5-substituted-1,3,4-oxadiazol-2-amine. Half of the substituted oxadiazole condensed with Bis-s-methyl ethylene cyanoacetmide and finally with 2,4-dinitro phenyl hydrazine HCl in ethanol gives 3-amino-1-(2,4-dinitro phenyl)-5-[(5-substituted-1,3,4-oxadiazol-2-yl)amino]-1-H-pyrazole-4carboxyamide. Half of the substituted oxadiazole condensed with oxazolone in pyridine gives (5E)-5[4-(dimethylamino) benzylidene]-3-(5-substituted-1,3,4-oxadiazol-2-yl)-2-phenyl-3,5-di hydro-4Himidazol-4-one. The identity of compounds were confirmed on the basis of their spectral data. All the compounds have been screened for their anthelmintic activity. </abstract>
<authors>Kalpesh Patel,Jayachandran E.,Ravi Shah,Vijaya Javali,Sreenivasa G. M.</authors>
<keywords>Semicarbazide, Oxadiazole,  Pyrazole,  Imidazole. </keywords>
<pages>-</pages>
</article>
</Journal>
