Ethyl 2-(tert-butoxy­carbonyl­amino)-1,3-benzothia­zole-6-carboxyl­ate

In the crystal of the title compound, C(15)H(18)N(2)O(4)S, inversion dimers are formed by inter­molecular N—H⋯N hydrogen bonds and weak C—H⋯O contacts. These dimers stack up along [100] through inversion-related π–π inter­actions between thia­zole rings [centroid–centroid distance = 3.790 (2) Å] and...

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Detalles Bibliográficos
Autores principales: Lei, Can, Fang, Xin, Yu, Hai-Yang, Huang, Ming-Dong, Wang, Jun-Dong
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2984018/
https://www.ncbi.nlm.nih.gov/pubmed/21580724
http://dx.doi.org/10.1107/S160053681001024X
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author Lei, Can
Fang, Xin
Yu, Hai-Yang
Huang, Ming-Dong
Wang, Jun-Dong
author_facet Lei, Can
Fang, Xin
Yu, Hai-Yang
Huang, Ming-Dong
Wang, Jun-Dong
author_sort Lei, Can
collection PubMed
description In the crystal of the title compound, C(15)H(18)N(2)O(4)S, inversion dimers are formed by inter­molecular N—H⋯N hydrogen bonds and weak C—H⋯O contacts. These dimers stack up along [100] through inversion-related π–π inter­actions between thia­zole rings [centroid–centroid distance = 3.790 (2) Å] and the thia­zole and benzene rings [centroid–centroid distance = 3.845 (2) Å] and C—H⋯π contacts.
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spelling pubmed-29840182010-12-30 Ethyl 2-(tert-butoxy­carbonyl­amino)-1,3-benzothia­zole-6-carboxyl­ate Lei, Can Fang, Xin Yu, Hai-Yang Huang, Ming-Dong Wang, Jun-Dong Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal of the title compound, C(15)H(18)N(2)O(4)S, inversion dimers are formed by inter­molecular N—H⋯N hydrogen bonds and weak C—H⋯O contacts. These dimers stack up along [100] through inversion-related π–π inter­actions between thia­zole rings [centroid–centroid distance = 3.790 (2) Å] and the thia­zole and benzene rings [centroid–centroid distance = 3.845 (2) Å] and C—H⋯π contacts. International Union of Crystallography 2010-03-24 /pmc/articles/PMC2984018/ /pubmed/21580724 http://dx.doi.org/10.1107/S160053681001024X Text en © Lei et al. 2010 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
Lei, Can
Fang, Xin
Yu, Hai-Yang
Huang, Ming-Dong
Wang, Jun-Dong
Ethyl 2-(tert-butoxy­carbonyl­amino)-1,3-benzothia­zole-6-carboxyl­ate
title Ethyl 2-(tert-butoxy­carbonyl­amino)-1,3-benzothia­zole-6-carboxyl­ate
title_full Ethyl 2-(tert-butoxy­carbonyl­amino)-1,3-benzothia­zole-6-carboxyl­ate
title_fullStr Ethyl 2-(tert-butoxy­carbonyl­amino)-1,3-benzothia­zole-6-carboxyl­ate
title_full_unstemmed Ethyl 2-(tert-butoxy­carbonyl­amino)-1,3-benzothia­zole-6-carboxyl­ate
title_short Ethyl 2-(tert-butoxy­carbonyl­amino)-1,3-benzothia­zole-6-carboxyl­ate
title_sort ethyl 2-(tert-butoxy­carbonyl­amino)-1,3-benzothia­zole-6-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2984018/
https://www.ncbi.nlm.nih.gov/pubmed/21580724
http://dx.doi.org/10.1107/S160053681001024X
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AT huangmingdong ethyl2tertbutoxycarbonylamino13benzothiazole6carboxylate
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