4-[(E)-2-Furylmethyl­eneamino]-3-phenyl-1H-1,2,4-triazole-5(4H)-thione

In the title mol­ecule, C(13)H(10)N(4)OS, the triazole ring makes dihedral angles of 16.14 (9) and 58.51 (11)°, respectively, with the phenyl and furan rings. Intra­molecular C—H⋯N hydrogen bonds generate S(5) and S(6) ring motifs. In the crystal structure, centrosymmetrically related mol­ecules are...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Jebas, Samuel Robinson, Sujith, K. V., Patil, P. S., Kalluraya, B., Dharmaprakash, S. M.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962152/
https://www.ncbi.nlm.nih.gov/pubmed/21203234
http://dx.doi.org/10.1107/S1600536808021806
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author Fun, Hoong-Kun
Jebas, Samuel Robinson
Sujith, K. V.
Patil, P. S.
Kalluraya, B.
Dharmaprakash, S. M.
author_facet Fun, Hoong-Kun
Jebas, Samuel Robinson
Sujith, K. V.
Patil, P. S.
Kalluraya, B.
Dharmaprakash, S. M.
author_sort Fun, Hoong-Kun
collection PubMed
description In the title mol­ecule, C(13)H(10)N(4)OS, the triazole ring makes dihedral angles of 16.14 (9) and 58.51 (11)°, respectively, with the phenyl and furan rings. Intra­molecular C—H⋯N hydrogen bonds generate S(5) and S(6) ring motifs. In the crystal structure, centrosymmetrically related mol­ecules are linked via N—H⋯S hydrogen bonds to form dimeric pairs, which are inter­linked via C—H⋯O and C—H⋯π inter­actions.
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spelling pubmed-29621522010-12-30 4-[(E)-2-Furylmethyl­eneamino]-3-phenyl-1H-1,2,4-triazole-5(4H)-thione Fun, Hoong-Kun Jebas, Samuel Robinson Sujith, K. V. Patil, P. S. Kalluraya, B. Dharmaprakash, S. M. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title mol­ecule, C(13)H(10)N(4)OS, the triazole ring makes dihedral angles of 16.14 (9) and 58.51 (11)°, respectively, with the phenyl and furan rings. Intra­molecular C—H⋯N hydrogen bonds generate S(5) and S(6) ring motifs. In the crystal structure, centrosymmetrically related mol­ecules are linked via N—H⋯S hydrogen bonds to form dimeric pairs, which are inter­linked via C—H⋯O and C—H⋯π inter­actions. International Union of Crystallography 2008-07-19 /pmc/articles/PMC2962152/ /pubmed/21203234 http://dx.doi.org/10.1107/S1600536808021806 Text en © Fun et al. 2008 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Fun, Hoong-Kun
Jebas, Samuel Robinson
Sujith, K. V.
Patil, P. S.
Kalluraya, B.
Dharmaprakash, S. M.
4-[(E)-2-Furylmethyl­eneamino]-3-phenyl-1H-1,2,4-triazole-5(4H)-thione
title 4-[(E)-2-Furylmethyl­eneamino]-3-phenyl-1H-1,2,4-triazole-5(4H)-thione
title_full 4-[(E)-2-Furylmethyl­eneamino]-3-phenyl-1H-1,2,4-triazole-5(4H)-thione
title_fullStr 4-[(E)-2-Furylmethyl­eneamino]-3-phenyl-1H-1,2,4-triazole-5(4H)-thione
title_full_unstemmed 4-[(E)-2-Furylmethyl­eneamino]-3-phenyl-1H-1,2,4-triazole-5(4H)-thione
title_short 4-[(E)-2-Furylmethyl­eneamino]-3-phenyl-1H-1,2,4-triazole-5(4H)-thione
title_sort 4-[(e)-2-furylmethyl­eneamino]-3-phenyl-1h-1,2,4-triazole-5(4h)-thione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962152/
https://www.ncbi.nlm.nih.gov/pubmed/21203234
http://dx.doi.org/10.1107/S1600536808021806
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