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Ethyl 5-acetyl-2-amino-4-methylthiophene-3-carboxylate
In the title compound, C(10)H(13)NO(3)S, prepared in a one-pot reaction, the molecular conformation is stabilized by an intramolecular N—H⋯O hydrogen bond. The packing is consolidated by further N—H⋯O links. The H atoms of two of the methyl groups are disordered over two sets of sites with equal o...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961554/ https://www.ncbi.nlm.nih.gov/pubmed/21202599 http://dx.doi.org/10.1107/S1600536808014177 |
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author | Akkurt, Mehmet Yıldırım, Sema Öztürk Asiri, Abdullah Mohamed McKee, Vickie |
author_facet | Akkurt, Mehmet Yıldırım, Sema Öztürk Asiri, Abdullah Mohamed McKee, Vickie |
author_sort | Akkurt, Mehmet |
collection | PubMed |
description | In the title compound, C(10)H(13)NO(3)S, prepared in a one-pot reaction, the molecular conformation is stabilized by an intramolecular N—H⋯O hydrogen bond. The packing is consolidated by further N—H⋯O links. The H atoms of two of the methyl groups are disordered over two sets of sites with equal occupancies. |
format | Text |
id | pubmed-2961554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29615542010-12-30 Ethyl 5-acetyl-2-amino-4-methylthiophene-3-carboxylate Akkurt, Mehmet Yıldırım, Sema Öztürk Asiri, Abdullah Mohamed McKee, Vickie Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(10)H(13)NO(3)S, prepared in a one-pot reaction, the molecular conformation is stabilized by an intramolecular N—H⋯O hydrogen bond. The packing is consolidated by further N—H⋯O links. The H atoms of two of the methyl groups are disordered over two sets of sites with equal occupancies. International Union of Crystallography 2008-05-17 /pmc/articles/PMC2961554/ /pubmed/21202599 http://dx.doi.org/10.1107/S1600536808014177 Text en © Akkurt 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 Akkurt, Mehmet Yıldırım, Sema Öztürk Asiri, Abdullah Mohamed McKee, Vickie Ethyl 5-acetyl-2-amino-4-methylthiophene-3-carboxylate |
title | Ethyl 5-acetyl-2-amino-4-methylthiophene-3-carboxylate |
title_full | Ethyl 5-acetyl-2-amino-4-methylthiophene-3-carboxylate |
title_fullStr | Ethyl 5-acetyl-2-amino-4-methylthiophene-3-carboxylate |
title_full_unstemmed | Ethyl 5-acetyl-2-amino-4-methylthiophene-3-carboxylate |
title_short | Ethyl 5-acetyl-2-amino-4-methylthiophene-3-carboxylate |
title_sort | ethyl 5-acetyl-2-amino-4-methylthiophene-3-carboxylate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961554/ https://www.ncbi.nlm.nih.gov/pubmed/21202599 http://dx.doi.org/10.1107/S1600536808014177 |
work_keys_str_mv | AT akkurtmehmet ethyl5acetyl2amino4methylthiophene3carboxylate AT yıldırımsemaozturk ethyl5acetyl2amino4methylthiophene3carboxylate AT asiriabdullahmohamed ethyl5acetyl2amino4methylthiophene3carboxylate AT mckeevickie ethyl5acetyl2amino4methylthiophene3carboxylate |