Synthesis and structural study of novel 5-aryl substituted 2-amino-4,7-dioxopyrido[2,3-d]pyrimidines |
| |
Authors: | Ren Rodríguez Margarita Surez Estael Ochoa Beatriz Pita Remberto Espinosa Nazario Martín Margarita Quinteiro Carlos Seoane Jose L Soto |
| |
Institution: | Rená Rodríguez,Margarita Suárez,Estael Ochoa,Beatriz Pita,Remberto Espinosa,Nazario Martín,Margarita Quinteiro,Carlos Seoane,Jose L. Soto |
| |
Abstract: | The tide compounds 4a-c have been prepared in a one-step procedure from 2,4-diamino-6-hydroxy-pyrimidine (1) and the corresponding arylidene substituted Meldrum's acids 2a-e in very good yields. Semiempirical theoretical calculations (AMI) reveal two favoured conformations ( A and B ) for compounds 4a-e. The 1H-nmr determinations, by using Karplus and Altona equations, clearly indicate that conformation A, with the aryl group on C5 in a pseudoaxial position, is that predominant in solution. The calculated charge density values for the olefinic carbons are in agreement with the experimental push-pull effect observed in the 13C-nmr spectra. |
| |
Keywords: | |
|
|