Abstract
Alkylation of 2-phenylamino-4-methylthiazole with substituted phenacyl bromides led to the synthesis of hydrobromides of 2-phenylimino-3-(p-R-phenacyl)-4-methylthiazoles. It was shown that, depending on the conditions of the cyclization of the last, 3-methyl-6-aryl-7-phenyl- or 3-methyl-5-aroyl-6-alkyl-7-phenylimidazo[2,1-b]thiazolium bromides can be synthesized. The spectral characteristics of the compounds synthesized were studied.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
