Catalytic synthesis of diazines from 1,3-diaminopropane and 3-amino-1-propanol

Autor: Oshis, Ya. F., Anderson, A. A., Shimanskaya, M. V.
Zdroj: Chemistry of Heterocyclic Compounds; July 1982, Vol. 18 Issue: 7 p740-745, 6p
Abstrakt: The transformations of 1,3-diaminopropane and 3-amino-1-propanol under pulse conditions over tungsten trioxide in an inert atmosphere at 300–500 °C were investigated. The transformation of 1,3-diaminopropane leads to the formation of saturated pyrimidine bases; the maximum selectivity of the formation of hexahydropyrimidine bases at 300 °C is 60%, while the selectivity of the formation of tetrahydropyrimidine bases is 20% (400 °C). In the case of 3-amino-1-propanol the overall yield of heterocyclic bases was less than 5%, and piperazine and pyrazine derivatives were observed as the cyclic products; the formation of pyrimidine bases was not observed.
Databáze: Supplemental Index