Abstract
1, 3-Disubstituted 5-acylamino-6-methyluracils ( 2a-e) were transformed into 1, 2-disubstituted 4-alkylcarbamoyl-5-methyl-1 H -imidazoles ( 3a-e) by treatment with 5% aqueous sodium hydroxide in ethanol. Similarly, reaction of 5-acylamino-6-methyl-3-phenyl-4-(3 H )-pyrimidinones ( 5a-d) with 5% aqueous sodium hydroxide in ethanol gave 2-substituted 5-methyl-4-phenylcarbamoyl-1 H -imidazoles ( 6a-d).
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.
