Synthesis and antiarrhythmic properties of N-acylamino derivatives of 1,6,7-substituted 1,2,3,4-tetrahydroisoquinoline-4-spirocyclopentanes and their analogs

Aseries of new N-chloracetyl derivatives have been synthesized proceeding from 4-spirocyclopentane-substituted 1,2,3,4-tetrahydroisoquinolines, 1-phenyl-1-cyclopentylmethylamine, and chloroanhydrides of bromoacetic and alpha -bromopropionic acids. Reactions of these bromoamides with amines (piperidi...

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Veröffentlicht in:Pharmaceutical chemistry journal 2006-07, Vol.40 (7), p.360-362
Hauptverfasser: Markaryan, É. A., Arustamyan, Zh. S., Avetisyan, S. V., Markaryan, R. É., Markaryan, K. Zh, Asatryan, T. O., Grigoryan, A. V.
Format: Artikel
Sprache:eng
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Zusammenfassung:Aseries of new N-chloracetyl derivatives have been synthesized proceeding from 4-spirocyclopentane-substituted 1,2,3,4-tetrahydroisoquinolines, 1-phenyl-1-cyclopentylmethylamine, and chloroanhydrides of bromoacetic and alpha -bromopropionic acids. Reactions of these bromoamides with amines (piperidine, morpholine) yield the title N-acylamino derivatives. The antiarrhythmic properties of the synthesized compounds have been studied.
ISSN:0091-150X
1573-9031
DOI:10.1007/s11094-006-0127-2