Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Reaction of β-Aminocrotonamide with N-Acylated Amino Acid Esters to give 2-Acylaminoalkyl-6-methylpyrimidin-4 (3H)-ones and Their Ring Closure with Polyphosphoric Acid (PPA)
NOBUYA KATAGIRIAKEMI KOSHIHARASHUGO ATSUUMITETSUZO KATO
Author information
Keywords: ^1H-NMR
JOURNAL FREE ACCESS

1983 Volume 31 Issue 7 Pages 2288-2295

Details
Abstract
Reaction of β-aminocrotonamide with N-acylated amino acid esters in the presence of sodium methoxide gave 2-acylaminoalkyl-6-methylpyrimidin-4 (3H)-ones, some of which, on treatment with polyphosphoric acid (PPA), were transformed into imidazo [1, 5-a] pyrimidines and imidazo [4, 5-b] pyridines.
Content from these authors
© The Pharmaceutical Society of Japan
Previous article Next article
feedback
Top