{"title":"Synthesis of Some New Pyrazolines via One-Pot Three Component Technique and Their Corresponding Thiazole Compounds","authors":"R. H. H. Salih, F. Hawaiz","doi":"10.24271/GARMIAN.159","DOIUrl":null,"url":null,"abstract":"In the present study; a one-pot three component reaction between4(4'-chlorobenzyloxy)acetophenone , thiosemicarbazide and different substituted benzaldehydes in absolute ethanolunder reflux with stirring has been used to give a new series of pyrazoline derivatives {3-(4-[4'-chlorobenzyloxy)phenyl)-5-(substituted-phenyl]-4,5-dihydropyrazole-1-carbothioamide}in highyields and short reaction times. . The later compounds were converted to their correspondingthiazole derivatives through reacting with 4-bromophenacyl bromide in ethanol. , The structures of the newly synthesized compounds were identified on the bases of their FT-IR, 1H-NMR, 13C-NMR and DEPT-135 spectra.","PeriodicalId":12283,"journal":{"name":"Evaluation Study of Three Diagnostic Methods for Helicobacter pylori Infection","volume":"55 1","pages":"505-518"},"PeriodicalIF":0.0000,"publicationDate":"2017-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Evaluation Study of Three Diagnostic Methods for Helicobacter pylori Infection","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.24271/GARMIAN.159","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
In the present study; a one-pot three component reaction between4(4'-chlorobenzyloxy)acetophenone , thiosemicarbazide and different substituted benzaldehydes in absolute ethanolunder reflux with stirring has been used to give a new series of pyrazoline derivatives {3-(4-[4'-chlorobenzyloxy)phenyl)-5-(substituted-phenyl]-4,5-dihydropyrazole-1-carbothioamide}in highyields and short reaction times. . The later compounds were converted to their correspondingthiazole derivatives through reacting with 4-bromophenacyl bromide in ethanol. , The structures of the newly synthesized compounds were identified on the bases of their FT-IR, 1H-NMR, 13C-NMR and DEPT-135 spectra.