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(Z)-4-{1-[(2-Hy­droxy­ethyl)­amino]­ethyl­idene}-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one

In the title compound C(14)H(17)N(3)O(2), the dihedral angle between the rings is 16.68 (13)°. Although the compound crystallizes in the keto form, the possibility of keto-enamine–enol-imine tautomerism is explained by a strong intra­molecular N—H⋯O hydrogen bond.

Detalles Bibliográficos
Autores principales: Jayarajan, R., Sharmila, P., Jagadeesan, G., Vasuki, G., Aravindhan, S.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051635/
https://www.ncbi.nlm.nih.gov/pubmed/21523108
http://dx.doi.org/10.1107/S1600536810054127
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author Jayarajan, R.
Sharmila, P.
Jagadeesan, G.
Vasuki, G.
Aravindhan, S.
author_facet Jayarajan, R.
Sharmila, P.
Jagadeesan, G.
Vasuki, G.
Aravindhan, S.
author_sort Jayarajan, R.
collection PubMed
description In the title compound C(14)H(17)N(3)O(2), the dihedral angle between the rings is 16.68 (13)°. Although the compound crystallizes in the keto form, the possibility of keto-enamine–enol-imine tautomerism is explained by a strong intra­molecular N—H⋯O hydrogen bond.
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spelling pubmed-30516352011-04-26 (Z)-4-{1-[(2-Hy­droxy­ethyl)­amino]­ethyl­idene}-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one Jayarajan, R. Sharmila, P. Jagadeesan, G. Vasuki, G. Aravindhan, S. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound C(14)H(17)N(3)O(2), the dihedral angle between the rings is 16.68 (13)°. Although the compound crystallizes in the keto form, the possibility of keto-enamine–enol-imine tautomerism is explained by a strong intra­molecular N—H⋯O hydrogen bond. International Union of Crystallography 2011-01-22 /pmc/articles/PMC3051635/ /pubmed/21523108 http://dx.doi.org/10.1107/S1600536810054127 Text en © Jayarajan et al. 2011 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
Jayarajan, R.
Sharmila, P.
Jagadeesan, G.
Vasuki, G.
Aravindhan, S.
(Z)-4-{1-[(2-Hy­droxy­ethyl)­amino]­ethyl­idene}-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one
title (Z)-4-{1-[(2-Hy­droxy­ethyl)­amino]­ethyl­idene}-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one
title_full (Z)-4-{1-[(2-Hy­droxy­ethyl)­amino]­ethyl­idene}-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one
title_fullStr (Z)-4-{1-[(2-Hy­droxy­ethyl)­amino]­ethyl­idene}-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one
title_full_unstemmed (Z)-4-{1-[(2-Hy­droxy­ethyl)­amino]­ethyl­idene}-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one
title_short (Z)-4-{1-[(2-Hy­droxy­ethyl)­amino]­ethyl­idene}-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one
title_sort (z)-4-{1-[(2-hy­droxy­ethyl)­amino]­ethyl­idene}-3-methyl-1-phenyl-1h-pyrazol-5(4h)-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051635/
https://www.ncbi.nlm.nih.gov/pubmed/21523108
http://dx.doi.org/10.1107/S1600536810054127
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