SYNTHESIS OF POSSIBLE NICOTINIC AGONISTS WITH POTENTIAL INSECTICIDE ACTIVITY

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Ethyl N-benzylpyridine-3-carboximidoate7 was prepared by reacting N-benzylnicotinamide and ethyl chloroformate, the other ethyl imidatehydrochloride, ethyl N-(2-phenylethyl) pyridine-3-carboximidoate8 , was prepared with the same method. Compound6 was obtained by synthesis of N-benzyl-N-(2-cyanoethy...

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Detalles Bibliográficos
Autores: Reyes García, Luis J., Cid, Pia
Formato: artículo
Fecha de Publicación:2016
Institución:Sociedad Química del Perú
Repositorio:Revista de la Sociedad Química del Perú
Lenguaje:español
OAI Identifier:oai:rsqp.revistas.sqperu.org.pe:article/121
Enlace del recurso:http://revistas.sqperu.org.pe/index.php/revistasqperu/article/view/121
Nivel de acceso:acceso abierto
Materia:Heterocycles synthesis
insecticidal activity
tetrahydropyrimidines
Síntesis heterociclos
actividad insecticida
tetrahidropirimidinas
Descripción
Sumario:Ethyl N-benzylpyridine-3-carboximidoate7 was prepared by reacting N-benzylnicotinamide and ethyl chloroformate, the other ethyl imidatehydrochloride, ethyl N-(2-phenylethyl) pyridine-3-carboximidoate8 , was prepared with the same method. Compound6 was obtained by synthesis of N-benzyl-N-(2-cyanoethyl) nicotinamide4 , the latter was used as a starting material to obtain N-(3-aminopropyl)-N-benzylnicotinamide5 by reduction with Ni-Raney in good yield. Cyclization reaction was obtained by p-toluenesulfonic acid of compound5 . Finally, compound (5,6-dihydro-2-(pyridin-3-yl)pyrimidin-1(4H)-yl)(2,4-dimethoxyphenyl) methanone9 was prepared by direct benzoylation of 1,4,5,6-tetrahydro-2-(pyridin-3-yl) pyrimidine.
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