4.5 Article

An Attempt to Achieve Hydrated Imidazoline Ring Expansion (HIRE) of Diarene-Fused [1,4]Diazepinones Delivers Selective Dopamine D2 Receptor Ligands

Journal

SYNTHESIS-STUTTGART
Volume 54, Issue 3, Pages 658-666

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/a-1649-5317

Keywords

[1,4]diazepinones; fused imidazolinium moiety; hydrated imidazoline ring expansion; 2-aminoethyl side chain expulsion; selective dopamine D-2 ligands

Funding

  1. Russian Science Foundation [19-75-30008]

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Attempts to extend the hydrated imidazoline ring expansion strategy to a series of diarene-fused [1,4]diazepinones did not lead to ring expansion but resulted in expulsion of the 2-aminoethyl side chain. This setback led to the discovery of selective dopamine D-2 ligands with elements of structure-activity relationships.
Attempts to extend the hydrated imidazoline ring expansion (HIRE) strategy to a series of diarene-fused [1,4]diazepinones (earlier applied successfully to bis-pyrido substrate nevirapine) did not result in ring expansion but, rather, led to 2-aminoethyl side chain expulsion. This seeming setback (setting the limitations to the HIRE methodology substrate scope) led to the discovery of selective dopamine D-2 ligands with elements of structure-activity relationships.

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