Synthesis and Properties of N,N′-Disubstituted Ureas and Their Isosteric Analogs Containing Polycyclic Fragments: XIX. exo-Isomers of N-(1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl)-N′-R-ureas and -thioureas

N , N ′-Disubstituted ureas and thioureas containing a 1,1,7-trimethylbicyclo[2.2.1]heptan-2-yl sub­stit­uent were synthesized in up to 99% yields by the reaction of exo -( R or S )-1,1,7-trimethylbicyclo[2.2.1]­heptan-2-amine with aromatic isocyanates and isothiocyanates with the goal of comprehens...

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Veröffentlicht in:Russian journal of organic chemistry 2024-03, Vol.60 (3), p.403-409
Hauptverfasser: Burmistrov, V. V., Kuznetsov, Ya. P., Novikov, V. V., Abbas, M. H. Saeef, Davidenko, A. V., Vernigora, A. A., Butov, G. M.
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Sprache:eng
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Zusammenfassung:N , N ′-Disubstituted ureas and thioureas containing a 1,1,7-trimethylbicyclo[2.2.1]heptan-2-yl sub­stit­uent were synthesized in up to 99% yields by the reaction of exo -( R or S )-1,1,7-trimethylbicyclo[2.2.1]­heptan-2-amine with aromatic isocyanates and isothiocyanates with the goal of comprehensive estimation of enantiomeric stereospecificity of human soluble epoxide hydrolase (hsEH). The synthesized compounds are promising hsEH inhibitors.
ISSN:1070-4280
1608-3393
DOI:10.1134/S1070428024030059