3-Benzyl­amino-2-cyano-N-[N-(2-fluoro­phenyl)­carbamo­yl]-3-(methyl­sulfanyl)acryl­amide

In the crystal structure of the title compound, C(19)H(17)FN(4)O(2)S, mol­ecules are linked via pairs of N—H⋯N inter­actions, forming centrosymmetric dimers. Two intra­molecular N—H⋯O hydrogen bonds stabilize the mol­ecular conformation.

Detalles Bibliográficos
Autores principales: Zhong, Shihua, Fan, Mingliang, Liu, Jianbing, Liu, Bingyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238891/
https://www.ncbi.nlm.nih.gov/pubmed/22199744
http://dx.doi.org/10.1107/S1600536811046125
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author Zhong, Shihua
Fan, Mingliang
Liu, Jianbing
Liu, Bingyu
author_facet Zhong, Shihua
Fan, Mingliang
Liu, Jianbing
Liu, Bingyu
author_sort Zhong, Shihua
collection PubMed
description In the crystal structure of the title compound, C(19)H(17)FN(4)O(2)S, mol­ecules are linked via pairs of N—H⋯N inter­actions, forming centrosymmetric dimers. Two intra­molecular N—H⋯O hydrogen bonds stabilize the mol­ecular conformation.
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spelling pubmed-32388912011-12-23 3-Benzyl­amino-2-cyano-N-[N-(2-fluoro­phenyl)­carbamo­yl]-3-(methyl­sulfanyl)acryl­amide Zhong, Shihua Fan, Mingliang Liu, Jianbing Liu, Bingyu Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(19)H(17)FN(4)O(2)S, mol­ecules are linked via pairs of N—H⋯N inter­actions, forming centrosymmetric dimers. Two intra­molecular N—H⋯O hydrogen bonds stabilize the mol­ecular conformation. International Union of Crystallography 2011-11-09 /pmc/articles/PMC3238891/ /pubmed/22199744 http://dx.doi.org/10.1107/S1600536811046125 Text en © Zhong 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
Zhong, Shihua
Fan, Mingliang
Liu, Jianbing
Liu, Bingyu
3-Benzyl­amino-2-cyano-N-[N-(2-fluoro­phenyl)­carbamo­yl]-3-(methyl­sulfanyl)acryl­amide
title 3-Benzyl­amino-2-cyano-N-[N-(2-fluoro­phenyl)­carbamo­yl]-3-(methyl­sulfanyl)acryl­amide
title_full 3-Benzyl­amino-2-cyano-N-[N-(2-fluoro­phenyl)­carbamo­yl]-3-(methyl­sulfanyl)acryl­amide
title_fullStr 3-Benzyl­amino-2-cyano-N-[N-(2-fluoro­phenyl)­carbamo­yl]-3-(methyl­sulfanyl)acryl­amide
title_full_unstemmed 3-Benzyl­amino-2-cyano-N-[N-(2-fluoro­phenyl)­carbamo­yl]-3-(methyl­sulfanyl)acryl­amide
title_short 3-Benzyl­amino-2-cyano-N-[N-(2-fluoro­phenyl)­carbamo­yl]-3-(methyl­sulfanyl)acryl­amide
title_sort 3-benzyl­amino-2-cyano-n-[n-(2-fluoro­phenyl)­carbamo­yl]-3-(methyl­sulfanyl)acryl­amide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238891/
https://www.ncbi.nlm.nih.gov/pubmed/22199744
http://dx.doi.org/10.1107/S1600536811046125
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AT fanmingliang 3benzylamino2cyanonn2fluorophenylcarbamoyl3methylsulfanylacrylamide
AT liujianbing 3benzylamino2cyanonn2fluorophenylcarbamoyl3methylsulfanylacrylamide
AT liubingyu 3benzylamino2cyanonn2fluorophenylcarbamoyl3methylsulfanylacrylamide

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