Three-component spiro heterocyclization of 1H-pyrrole-2,3-diones with acetonitriles and 4-hydroxycoumarin. Crystal and molecular structure of ethyl 2-amino-3-cyano-1′-cyclohexyl-2′,5-dioxo-5′-phenyl-1′,2′-dihydro-5H-spiro-[pyrano[3,2-c]chromene-4,3′-pyrrole]-4′-carboxylate View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2015-01

AUTHORS

M. V. Dmitriev, P. S. Silaichev, A. N. Maslivets

ABSTRACT

Ethyl 4,5-dioxo-2-phenyl-4,5-dihydro-1H-pyrrole-3-carboxylates reacted with malononitrile (methyl cyanoacetate) and 4-hydroxycoumarin to produce substituted ethyl 2-amino-2′,5-dioxo-5′-phenyl-1′,2′-dihydro-5H-spiro[pyrano[3,2-c]chromene-4,3′-pyrrole]-4′-carboxylates. The crystal and molecular structure of ethyl 2-amino-3-cyano-1′-cyclohexyl-2′,5-dioxo-5′-phenyl-1′,2′-dihydro-5H-spiro[pyrano[3,2-c]chromene-4,3′-pyrrole]-4′-carboxylate was determined by X-ray analysis.

PAGES

74-77

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070428015010121

DOI

http://dx.doi.org/10.1134/s1070428015010121

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1035346549


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