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Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4662
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dc.contributor.authorPatil, SB
dc.contributor.authorBasha, NJ
dc.contributor.authorGoudgaon, NM
dc.date.accessioned2020-06-12T15:04:30Z-
dc.date.available2020-06-12T15:04:30Z-
dc.date.issued2010
dc.identifier.citationINDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY , Vol. 19 , 3 , p. 307 - 308en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4662-
dc.description.abstractReaction of 2-hydrazinobenzimidazole (1) with 3-aryl-1-phenyl-1H-pyrazole-4-carbaldehydes (2a-f) in ethanol yielded the corresponding Schiff's bases (3a-f). Further, cyclization of compounds 3a-f with thioglycollic acid in benzene in presence of anhyd ZnCl(2) furnished desired compounds 3-(benzo [d] imidazol-2-ylamino)-2-(3-aryl-1-phenyl-1H-pyrazol-4-y1) thiazolidin-4-ones (4a-f) in 41-65% yield. All the synthesized compounds were characterized by the spectral data such as IR, (1)H NMR, mass and elemental analysis.en_US
dc.publisherDR R S VARMA
dc.titleSYNTHESIS OF NEW 3-(BENZO [d] IMIDAZOL-2-YL AMINO)-2-(3-ARYL-1-PHENYL-1H-PYRAZOL-4-YL) THIAZOLIDIN-4-ONESen_US
dc.typeArticle
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