Reaction of 3-Amino-4,6-diarylthieno[2,3-b]pyridine-2-carboxamides with Ninhydrin

The reaction of N -substituted amides of 3-amino-4,6-diarylthieno[2,3- b ]pyridine-2-carboxylic acids with ninhydrin in the presence of catalytic amounts of sulfuric acid gave 1′-spiro[indene-2,2′-pyrido[3′,2′:4,5]thieno[3,2- d ]pyrimidine]-1,3,4′(3′ H )-triones. Structure of a number of key compoun...

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Veröffentlicht in:Russian journal of general chemistry 2020-06, Vol.90 (6), p.948-960
Hauptverfasser: Dotsenko, V. V., Muraviev, V. S., Lukina, D. Yu, Strelkov, V. D., Aksenov, N. A., Aksenova, I. V., Krapivin, G. D., Dyadyuchenko, L. V.
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Sprache:eng
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Zusammenfassung:The reaction of N -substituted amides of 3-amino-4,6-diarylthieno[2,3- b ]pyridine-2-carboxylic acids with ninhydrin in the presence of catalytic amounts of sulfuric acid gave 1′-spiro[indene-2,2′-pyrido[3′,2′:4,5]thieno[3,2- d ]pyrimidine]-1,3,4′(3′ H )-triones. Structure of a number of key compounds was studied using 2D NMR spectroscopy; the bioavailability parameters of the obtained compounds in silico were calculated. In a laboratory experiment, a moderate antidote effect was revealed with respect to the 2,4-D herbicide for one compound.
ISSN:1070-3632
1608-3350
DOI:10.1134/S1070363220060043