Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Dimethylamination and Nitrosation of Pyrimidines with N-Nitrosodimethylamine
FUMIO YONEDAKEITARO SENGASADAO NISHIGAKI
Author information
JOURNAL FREE ACCESS

1973 Volume 21 Issue 2 Pages 260-263

Details
Abstract
Reaction of a chloropyrimidine and a 5-activated pyrimidine in N-nitrosodimethylamine (NDA) resulted in the simultaneous formation of a dimethylaminopyrimidine and a 5-nitrosopyrimidine which is further transformed. A special type of Vilsmeier-Haack reaction using a mixture of NDA and phosphorus oxychloride (NDA+POCl3) for 5-activated pyrimidines has been accomplished. The reaction of 6-amino-1, 3-dimethyluracil with NDA+POCl3 under cooling gave bis (6-amino-1, 3-dimethyluracil-5-yl) methane, which was converted into 1, 3, 7, 9-tetramethyl (1H, 3H, 7H, 9H)-pyrido [2, 3-d, 6, 5-d'] dipyrimidine-2, 4, 6, 8-tetrone.
Content from these authors
© The Pharmaceutical Society of Japan
Previous article Next article
feedback
Top