Cyclization of monosubstituted triaminopyrimidines with acetic acid imino ester hydrochloride |
| |
Authors: | V M Cherkasov L K Kurilenko |
| |
Institution: | (1) Institute of Organic Chemistry, Academy of Sciences of the Ukrainian SSR, Kiev |
| |
Abstract: | 6-N-Substituted 6-amino-8-methylpurines and 6-amino-8-methyl-9-substituted purines were obtained by cyclization of 6-N-substituted 4,5,6-triaminopyrimidines with acetic acid imino ester hydrochloride. The yields of the isomers depend on the different basicities of the secondary amino groups, which are determined by the basicities of the starting amines. The yields of the 6-amino-8-methyl-9-substituted purines increase with decreasing basicity.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1432–1434, October, 1970. |
| |
Keywords: | |
本文献已被 SpringerLink 等数据库收录! |
|