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Mol Divers ; 21(4): 925-932, 2017 11.
Article in English | MEDLINE | ID: mdl-28766257

ABSTRACT

A multicomponent domino synthesis has been developed for the preparation of 2-aminopyrimidines from ß-dicarbonyl compounds, N,N-dimethylformamide dimethyl acetal, and cyanamide. The protocol was used for the regioselective preparation of 4-amide/ester/ketone substituted 2-aminopyrimidines. Twelve 2-aminopyrimidines were isolated in good yields (56-93%).


Subject(s)
Cyanamide/chemistry , Dimethylformamide/analogs & derivatives , Pyrimidines/chemistry , Pyrimidines/chemical synthesis , Catalysis , Chemistry Techniques, Synthetic , Cyclization , Dimethylformamide/chemistry , Stereoisomerism
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