Cyclocondensation of 2,2-dichloroethenylbenzamide and its analogs with amidines and hydrogen sulfide in the presence of bases View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2009-03

AUTHORS

B. A. Demidchuk, S. O. Seferov, A. N. Vasilenko, V. S. Brovarets, B. S. Drach

ABSTRACT

Available chlorine-containing enamides of the general formula Cl2C=CHNHCOR (I) easily react with benzamidine and its derivatives to give 1:1 adducts which under heating with sodium methylate transform to 2-(methoxymethyl)-4,5-diaryl-s-triazines. Reaction of compounds (I) with hydrogen sulfide in the presence of triethylamine yields a mixture of products. Only the corresponding 3,5-bis(acylaminomethyl)-1,2,4-tritiolanes were isolated from the reaction mixture in moderate yield. More... »

PAGES

500-504

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070363209030268

DOI

http://dx.doi.org/10.1134/s1070363209030268

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1020791970


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