Reaction of 2-aryl-4-dichloromethylidene-1,3-oxazol-5(4H)-ones with 2-aminopyridine View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2010-01

AUTHORS

V. M. Prokopenko, S. G. Pil’o, V. S. Brovarets, A. N. Vasilenko, B. S. Drach

ABSTRACT

Reactions of multicenter electrophilic substrates, 2-aryl-4-dichloromethylidene-1,3-oxazol-5(4H)-ones, with 2-aminopyridine, involved cleavage of the dihydrooxazole ring by the primary amino group of nucleophilic reagent and subsequent cyclization to imidazopyridine derivatives. The latter reacted with morpholine and its analogs via recyclization with formation of 5-amino-2-aryl-N-(pyridin-2-yl)-1,3-oxazole-4-carboxamides.

PAGES

121-126

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070363210010160

DOI

http://dx.doi.org/10.1134/s1070363210010160

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1032047359


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