Synthesis and structure of new pyrido[2,3-D]pyrimidine derivatives with calcium-channel antagonist activity

Several series of pyrido[2,3-d]pyrimidine derivatives were synthesized by reaction of aryl methyleneacetoacetates with different aminopyrimidines. The solid-state structure of the methyl 5-(3'-chlorophenyl)-7-methyl-4-oxo-2-thioxo-1,2,3,4,5,8-hexahydropyrido[ 2,3-d]pyrimidine-6-carboxylate show...

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Detalles Bibliográficos
Autores: Pastor del Castillo, Alfredo, Alajarín Ferrández, Luis Ramón|||0000-0002-7573-8013, Vaquero López, Juan José|||0000-0002-3820-9673, Álvarez-Builla Gómez, Julio, Casa-Juana Muñoz, Miguel Fau de, Sunkel Letelier, Carlos, Priego, J.G., Fonseca, I., Sanz-Aparicio, Julia
Tipo de recurso: artículo
Fecha de publicación:1994
País:España
Institución:Universidad de Alcalá (UAH)
Repositorio:e_Buah Biblioteca Digital Universidad de Alcalá
Idioma:inglés
OAI Identifier:oai:ebuah.uah.es:10017/3697
Acceso en línea:http://hdl.handle.net/10017/3697
https://dx.doi.org/10.1016/S0040-4020(01)85291-1
Access Level:acceso abierto
Palabra clave:Pyrido[2,3-D]pyrimidine derivatives
Calcium-channel
Ciencia
Química orgánica
Science
Chemistry, organic
Descripción
Sumario:Several series of pyrido[2,3-d]pyrimidine derivatives were synthesized by reaction of aryl methyleneacetoacetates with different aminopyrimidines. The solid-state structure of the methyl 5-(3'-chlorophenyl)-7-methyl-4-oxo-2-thioxo-1,2,3,4,5,8-hexahydropyrido[ 2,3-d]pyrimidine-6-carboxylate shows that these compounds can adopt some of the most important structural features of the 1,4-dihydropyridine calcium channel blockers. The scope and limitations of the synthetic procedure with different aminoheterocycles is presented together with the initial evaluation of their calcium antagonistic activity by comparison with the usual reference compound nifedipine.