Synlett 2018; 29(11): 1502-1504
DOI: 10.1055/s-0036-1591991
letter
© Georg Thieme Verlag Stuttgart · New York

Synthetic Approach Toward Heterocyclic Hybrids of [1,2,4]Triazolo[3,4-b][1,3,4]thiadiazines

Nawel Lechani
a   Laboratoire de Chimie Organique Appliquée, Faculté de Chimie, Université des Sciences et de la Technologie Houari Boumediène BP 32, El-Alia Bab-Ezzouar, 16111 Alger, Algeria   Email: prhamdi@gmail.com
b   Département de Chimie, Faculté des Sciences, Université Saad Dahleb, Blida, Algeria
,
Maamar Hamdi*
a   Laboratoire de Chimie Organique Appliquée, Faculté de Chimie, Université des Sciences et de la Technologie Houari Boumediène BP 32, El-Alia Bab-Ezzouar, 16111 Alger, Algeria   Email: prhamdi@gmail.com
,
Baya Kheddis-Boutemeur
a   Laboratoire de Chimie Organique Appliquée, Faculté de Chimie, Université des Sciences et de la Technologie Houari Boumediène BP 32, El-Alia Bab-Ezzouar, 16111 Alger, Algeria   Email: prhamdi@gmail.com
,
Oualid Talhi*
c   Centre de Recherche Scientifique et Technique en Analyses Physico-Chimiques, BP 384, Bou-Ismail, 42004 Tipaza, Algeria
d   QOPNA and Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal   Email: oualid.talhi@ua.pt   Email: artur.silva@ua.pt
,
Yacine Laichi
c   Centre de Recherche Scientifique et Technique en Analyses Physico-Chimiques, BP 384, Bou-Ismail, 42004 Tipaza, Algeria
,
Khaldoun Bachari
c   Centre de Recherche Scientifique et Technique en Analyses Physico-Chimiques, BP 384, Bou-Ismail, 42004 Tipaza, Algeria
,
d   QOPNA and Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal   Email: oualid.talhi@ua.pt   Email: artur.silva@ua.pt
› Author Affiliations
Thanks are due to the University of Aveiro and FCT/MEC for financial support to the QOPNA research project (FCT UID/QUI/00062/2013), financed by national funds and, when appropriate, co-financed by FEDER under the PT2020 Partnership Agreement. Thanks are also due to the Portuguese NMR Network. We would also like to thank FCT/MEC and the General Directorate for Scientific Research and Technological Development – DGRSDT of Algeria and the Agence Thématique de Recherche en Sciences et Technologie ATRST for approving the co-financed bilateral project PT-DZ/0005.
Further Information

Publication History

Received: 10 March 2018

Accepted: 24 March 2018

Publication Date:
23 April 2018 (online)


Abstract

The synthesis of novel heterocyclic [1,2,4]triazolo[3,4-b][1,3,4]thiadiazine hybrids by a bimolecular reaction of 2-(4-amino-5-mercapto-4H-[1,2,4]triazol-3-yl)phenol with an aromatic or heterocyclic α-bromoacetyl derivatives is described. This synthetic procedure starts from an unprotected phenol.

Supporting Information

 
  • References and Notes

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    • 4b Talhi O. Abdeldjebar H. Belmiloud Y. Hassaine R. Taibi N. Válega M. Paz FA. A. Brahimi M. Bachari K. Silva AM. S. New J. Chem. 2017; 41: 10790
    • 4c Bouhenna MM. Orlikova B. Talhi O. Schram B. Pinto DC. G. A. Taibi N. Bachari K. Diederich M. Silva AM. S. Mameri N. Anticancer Res. 2017; 37: 5225
    • 4d Lee J.-Y. Talhi O. Jang D. Cerella C. Gaigneaux A. Kim K.-W. Lee JW. Dicato M. Bachari K. Han BW. Silva AM. S. Orlikova B. Diederich M. Cancer Lett. 2018; 416: 94
  • 8 [1,2,4]Triazolo[3,4-b][1,3,4]thiadiazines 3ae; General Procedure Equimolar amounts of the appropriate α-bromoacetyl derivative 2ae (1.0 mmol) and triazolylphenol 1 (0.2 g; 1.0 mmol) were dissolved in absolute EtOH (10 mL) containing a catalytic amount of AcOH (1 mL), and the mixture was heated for 2 h, then cooled to r.t. The resulting solid was collected by filtration and washed with EtOH and Et2O to give the pure product.
  • 9 7-Hydroxy-3-[3-(2-hydroxyphenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-6-yl]-2H-chromen-2-one (3b) C19H12N4O4S. Green solid; yield: 0.23 g (60%); mp 239–241 °C. 1H NMR (400 MHz, DMSO-d 6): δ = 5.00 (s, 2 H, H-7′), 6.80 (d, J = 2.2 Hz, 1 H, H-8), 6.89 (dd, J = 8.6, 2.2 Hz, 1 H, H-6), 6.93–7.01 (m, 1 H, H-5′′), 7.06 (dd, J = 8.3, 0.7 Hz, 1 H, H-3′′), 7.41–7.46 (m, 1 H, H-4′′), 7.71 (dd, J = 7.8, 1.7 Hz, 1 H, H-6′′), 7.85 (d, J = 8.6 Hz, 1 H, H-5), 8.77 (s, 1 H, H-4), 10.23 (s, 1 H, 2′′-OH), 11.33 (s, 1 H, 7-OH). 13C NMR (100 MHz, DMSO-d 6): δ = 44.0 (C-7′), 102.4 (C-8), 110.0 (C-1′′), 111.4 (C-4a), 115.1 (C-6), 117.7 (C-3′′), 117.9 (C-3), 120.1 (C-5′′), 129.3 (C-6′′), 133.6 and 133.7 (C-4′′ and C-5), 149.9 (C-4), 156.5 (C-2′′), 158.0 (C-8a), 159.6 (C-2), 163.3 (C-8′a), 164.9 (C-3′, C=N), 165.4 (C-7), 189.9 (C-6′, C=N). HRMS-ESI+: m/z [M + H]+ calcd for C19H13N4O4S: 393.0658; found: 393.0677.