Synthesis of New Tetracyclic Ring Systems: Bridged Derivatives of Hydroxy‐, Sulfanyl‐ and Amino‐Substituted Dibenzo[c,<i>f</i>][1,2]Thiazepine <i>S</i>,<i>S</i>‐Dioxides

Abstract In continuation of our commitment to the synthesis of new ring systems based on the 6,11‐dihydrodibenzo[ c , f ][1,2]thiazepine 5,5‐dioxide core of the antidepressant drug tianeptine, we have incorporated two‐ and/or three‐carbon bridges between the nitrogen atom of the sulfonamide moiety and the N ‐, O ‐ or S ‐substituent at position 11 of the tricycle. The synthesis of 5 new ring systems is described and demonstrated with several target compounds.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-09-27
DOI
https://doi.org/10.1002/ejoc.202400835
Citations
2
Primary Topic
Phenothiazines and Benzothiazines Synthesis and Activities
Type
article
Field-Weighted Citation Impact
0.47

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article

Synthesis of New Tetracyclic Ring Systems: Bridged Derivatives of Hydroxy‐, Sulfanyl‐ and Amino‐Substituted Dibenzo[c,f][1,2]Thiazepine S,S‐Dioxides

Lóránd Kiss, András Dancsó, Balázs Volk, Mária Tóthné Lauritz et al.
2 citations
European Journal of Organic Chemistry
Phenothiazines and Benzothiazines Synthesis and Activities
0.47
article

Synthesis of New Tetracyclic Ring Systems: Bridged Derivatives of Hydroxy‐, Sulfanyl‐ and Amino‐Substituted Dibenzo[c,f][1,2]Thiazepine S,S‐Dioxides

Lóránd Kiss, András Dancsó, Balázs Volk, Mária Tóthné Lauritz, Gyula Simig, Gábor Berecz, Dávid Szabó
article en
2 citations

Abstract

Abstract In continuation of our commitment to the synthesis of new ring systems based on the 6,11‐dihydrodibenzo[ c , f ][1,2]thiazepine 5,5‐dioxide core of the antidepressant drug tianeptine, we have incorporated two‐ and/or three‐carbon bridges between the nitrogen atom of the sulfonamide moiety and the N ‐, O ‐ or S ‐substituent at position 11 of the tricycle. The synthesis of 5 new ring systems is described and demonstrated with several target compounds.

European Journal of Organic ChemistryVol. 27(46)
Egis Pharmaceuticals (Hungary) (HU), HUN-REN Research Centre for Natural Sciences (HU)
Nemzeti Kutatási, Fejlesztési és Innovaciós Alap
Openalex Percentile: Top 35%
Phenothiazines and Benzothiazines Synthesis and Activities
0.47
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