Synthesis of some amino-substituted furanopyrimidines and styrylpyrimidines†
暂无分享,去创建一个
5-p-Chlorophenyl-6,6-dimethyl-5,6-dihydro-3H-furano[2,3-d]pyrimidine-4-one is readily converted to 4,6-dichloro-5-β-β-dimethyl-α- (p-chlorostyryl)pyrimidine by warming in phosphorus oxychloride and acetic acid, behavior which is in strong contrast to that of the analogous 5-phenyl derivative. The reaction provides a convenient source of 4-amino-6-chloro-5β,β-dimethyl-α- (p-chlorostyryl)pyrimidines and 4,6-diamino-5-β,β-dimethyl-α- (p-chlorostyryl)pyrimidines, compounds of potential biological interest.
[1] E. Campaigne,et al. Novel animation reactions of dihydrofurano[2,3-d] pyrimidines† , 1970 .
[2] R. L. Ellis,et al. Synthesis of substituted 2-amino-3-cyanodihydrofurans from styrene oxides and malononitrile , 1969 .
[3] R. L. Ellis,et al. Synthesis of some ureidodihydrofurans and related pyrimidones as potential antimalarials. , 1969, Journal of medicinal chemistry.
[4] P. Russell,et al. 2,4,7-Triamino-6-ortho-substituted Arylpteridines. A New Series of Potent Antimalarial Agents. , 1967, Journal of medicinal chemistry.