Synthesis and Anticoagulant Activity of New Ethylidene and Spiro Derivatives of Pyrrolo[3,2,1-ij]quinolin-2-ones

The reaction of pyrrolo[3,2,1- ij ]quinoline-1,2-diones with methyl (het)aryl ketones gave the corresponding 1-(het)arylmethylidenepyrroloquinolin-2-ones, and 1,3-dipolar cycloaddition of the latter to azomethine ylide generated from sarcosine and paraformaldehyde afforded 4-acyl-1,4′,4′,6′-tetramet...

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Veröffentlicht in:Russian journal of organic chemistry 2020-09, Vol.56 (9), p.1550-1556
Hauptverfasser: Novichikhina, N. P., Skoptsova, A. A., Shestakov, A. S., Potapov, A. Yu, Kosheleva, E. A., Kozaderov, O. A., Ledenyova, I. V., Podoplelova, N. A., Panteleev, M. A., Shikhaliev, Kh. S.
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Sprache:eng
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Zusammenfassung:The reaction of pyrrolo[3,2,1- ij ]quinoline-1,2-diones with methyl (het)aryl ketones gave the corresponding 1-(het)arylmethylidenepyrroloquinolin-2-ones, and 1,3-dipolar cycloaddition of the latter to azomethine ylide generated from sarcosine and paraformaldehyde afforded 4-acyl-1,4′,4′,6′-tetramethylspiro[pyrrolidine-3,1′-pyrrolo[3,2,1- ij ]quinolin]-2′(4′H)-ones. The synthesized compounds were evaluated for inhibitory activity against blood coagulation factors Xa and XIa.
ISSN:1070-4280
1608-3393
DOI:10.1134/S1070428020090080