tert-Butyl 3-carbamoyl-4-methoxy­imino-3-methyl­piperidine-1-carboxyl­ate

In the title compound, C(13)H(23)N(3)O(4), the piperidine ring adopts a chair conformation. An intra­molecular N—H⋯O hydrogen bond is observed between the carbamoyl and carboxyl­ate groups. In the crystal structure, mol­ecules form inversion dimers linked by pairs of N—H⋯O hydrogen bonds.

Detalles Bibliográficos
Autores principales: Chai, Yun, Wan, Zhi-Long, Guo, Hui-Yuan, Liu, Ming-Liang
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968237/
https://www.ncbi.nlm.nih.gov/pubmed/21581895
http://dx.doi.org/10.1107/S1600536809000634
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author Chai, Yun
Wan, Zhi-Long
Guo, Hui-Yuan
Liu, Ming-Liang
author_facet Chai, Yun
Wan, Zhi-Long
Guo, Hui-Yuan
Liu, Ming-Liang
author_sort Chai, Yun
collection PubMed
description In the title compound, C(13)H(23)N(3)O(4), the piperidine ring adopts a chair conformation. An intra­molecular N—H⋯O hydrogen bond is observed between the carbamoyl and carboxyl­ate groups. In the crystal structure, mol­ecules form inversion dimers linked by pairs of N—H⋯O hydrogen bonds.
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spelling pubmed-29682372010-12-30 tert-Butyl 3-carbamoyl-4-methoxy­imino-3-methyl­piperidine-1-carboxyl­ate Chai, Yun Wan, Zhi-Long Guo, Hui-Yuan Liu, Ming-Liang Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(23)N(3)O(4), the piperidine ring adopts a chair conformation. An intra­molecular N—H⋯O hydrogen bond is observed between the carbamoyl and carboxyl­ate groups. In the crystal structure, mol­ecules form inversion dimers linked by pairs of N—H⋯O hydrogen bonds. International Union of Crystallography 2009-01-10 /pmc/articles/PMC2968237/ /pubmed/21581895 http://dx.doi.org/10.1107/S1600536809000634 Text en © Chai et al. 2009 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
Chai, Yun
Wan, Zhi-Long
Guo, Hui-Yuan
Liu, Ming-Liang
tert-Butyl 3-carbamoyl-4-methoxy­imino-3-methyl­piperidine-1-carboxyl­ate
title tert-Butyl 3-carbamoyl-4-methoxy­imino-3-methyl­piperidine-1-carboxyl­ate
title_full tert-Butyl 3-carbamoyl-4-methoxy­imino-3-methyl­piperidine-1-carboxyl­ate
title_fullStr tert-Butyl 3-carbamoyl-4-methoxy­imino-3-methyl­piperidine-1-carboxyl­ate
title_full_unstemmed tert-Butyl 3-carbamoyl-4-methoxy­imino-3-methyl­piperidine-1-carboxyl­ate
title_short tert-Butyl 3-carbamoyl-4-methoxy­imino-3-methyl­piperidine-1-carboxyl­ate
title_sort tert-butyl 3-carbamoyl-4-methoxy­imino-3-methyl­piperidine-1-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968237/
https://www.ncbi.nlm.nih.gov/pubmed/21581895
http://dx.doi.org/10.1107/S1600536809000634
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AT wanzhilong tertbutyl3carbamoyl4methoxyimino3methylpiperidine1carboxylate
AT guohuiyuan tertbutyl3carbamoyl4methoxyimino3methylpiperidine1carboxylate
AT liumingliang tertbutyl3carbamoyl4methoxyimino3methylpiperidine1carboxylate

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