Fused pyrimidine systems: XIV. Reaction of 2-alkenyl(alkynyl)sulfanylpyrido[3,4-d]pyrimidin-4(3H)-ones with arylsulfanyl chlorides View Full Text


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Article Info

DATE

2014-06

AUTHORS

I. V. Dyachenko, A. I. Vas’kevich, R. I. Vas’kevich, M. V. Vovk

ABSTRACT

2-Allylsulfanylpyrido[3,4-d]pyrimidin-4(3H)-one reacted with arylsulfanyl chlorides in chloroform to give addition products to the exocyclic double bond, which were converted into linearly fused arylsulfanylthiazinopyridopyrimidines by the action of sodium acetate. The reactions of 2-allyl(cinnamyl, propargyl)sulfanylpyrido[3,4-d]pyrimidin-4(3H)-ones with arylsulfanyl chlorides in the presence of an equimolar amount of lithium perchlorate afforded angularly fused arylsulfanylmethylthiazolo- and -thiazinopyridopyrimidines. More... »

PAGES

858-863

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070428014060189

DOI

http://dx.doi.org/10.1134/s1070428014060189

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1026809104


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