Ethyl 6-(4-cyclo­propyl-1H-1,2,3-triazol-1-yl)pyridine-3-carboxyl­ate

In the title compound, C(13)H(14)N(4)O(2), which has approximate mirror symmetry, the dihedral angles between the triazole ring and the cyclo­propane and pyridine rings are 87.1 (2) and 7.60 (9)°, respectively. In the crystal, inversion dimers linked by pairs of both C—H⋯N and C—H⋯O inter­actions ge...

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Autores principales: Ahmed, Muhammad Naeem, Yasin, Khawaja Ansar, Tahir, M. Nawaz, Bibi, Asma, Andleeb, Hina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2014
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998301/
https://www.ncbi.nlm.nih.gov/pubmed/24764862
http://dx.doi.org/10.1107/S1600536813034673
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author Ahmed, Muhammad Naeem
Yasin, Khawaja Ansar
Tahir, M. Nawaz
Bibi, Asma
Andleeb, Hina
author_facet Ahmed, Muhammad Naeem
Yasin, Khawaja Ansar
Tahir, M. Nawaz
Bibi, Asma
Andleeb, Hina
author_sort Ahmed, Muhammad Naeem
collection PubMed
description In the title compound, C(13)H(14)N(4)O(2), which has approximate mirror symmetry, the dihedral angles between the triazole ring and the cyclo­propane and pyridine rings are 87.1 (2) and 7.60 (9)°, respectively. In the crystal, inversion dimers linked by pairs of both C—H⋯N and C—H⋯O inter­actions generate R (2) (2)(6) and R (2) (2)(18) loops, respectively. Further C—H⋯N inter­actions form R (2) (2)(10) loops and link the dimers into [110] chains.
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spelling pubmed-39983012014-04-24 Ethyl 6-(4-cyclo­propyl-1H-1,2,3-triazol-1-yl)pyridine-3-carboxyl­ate Ahmed, Muhammad Naeem Yasin, Khawaja Ansar Tahir, M. Nawaz Bibi, Asma Andleeb, Hina Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(14)N(4)O(2), which has approximate mirror symmetry, the dihedral angles between the triazole ring and the cyclo­propane and pyridine rings are 87.1 (2) and 7.60 (9)°, respectively. In the crystal, inversion dimers linked by pairs of both C—H⋯N and C—H⋯O inter­actions generate R (2) (2)(6) and R (2) (2)(18) loops, respectively. Further C—H⋯N inter­actions form R (2) (2)(10) loops and link the dimers into [110] chains. International Union of Crystallography 2014-01-15 /pmc/articles/PMC3998301/ /pubmed/24764862 http://dx.doi.org/10.1107/S1600536813034673 Text en © Ahmed et al. 2014 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
Ahmed, Muhammad Naeem
Yasin, Khawaja Ansar
Tahir, M. Nawaz
Bibi, Asma
Andleeb, Hina
Ethyl 6-(4-cyclo­propyl-1H-1,2,3-triazol-1-yl)pyridine-3-carboxyl­ate
title Ethyl 6-(4-cyclo­propyl-1H-1,2,3-triazol-1-yl)pyridine-3-carboxyl­ate
title_full Ethyl 6-(4-cyclo­propyl-1H-1,2,3-triazol-1-yl)pyridine-3-carboxyl­ate
title_fullStr Ethyl 6-(4-cyclo­propyl-1H-1,2,3-triazol-1-yl)pyridine-3-carboxyl­ate
title_full_unstemmed Ethyl 6-(4-cyclo­propyl-1H-1,2,3-triazol-1-yl)pyridine-3-carboxyl­ate
title_short Ethyl 6-(4-cyclo­propyl-1H-1,2,3-triazol-1-yl)pyridine-3-carboxyl­ate
title_sort ethyl 6-(4-cyclo­propyl-1h-1,2,3-triazol-1-yl)pyridine-3-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998301/
https://www.ncbi.nlm.nih.gov/pubmed/24764862
http://dx.doi.org/10.1107/S1600536813034673
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