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Crystal structure of methyl 3′-benzamido-4′-(4-meth­oxy­phen­yl)-1′-methyl­spiro­[indeno­[1,2-b]quinoxaline-11,2′-pyrrolidine]-3′-carboxyl­ate

In the title compound, C(35)H(30)N(4)O(3), the spiro C atom connects the five-membered pyrrolidine ring and the indeno­quinoxaline ring system. The pyrrolidine ring adopts a twist conformation. An intra­molecular N—H⋯N inter­action between the amino group and the pyrazine ring is observed. In the cr...

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Autores principales: Chandralekha, Kuppan, Sureshbabu, Adukamparai Rajukrishnan, Gavaskar, Deivasigamani, Lakshmi, Srinivasakannan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120701/
https://www.ncbi.nlm.nih.gov/pubmed/27920911
http://dx.doi.org/10.1107/S2056989016012469
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author Chandralekha, Kuppan
Sureshbabu, Adukamparai Rajukrishnan
Gavaskar, Deivasigamani
Lakshmi, Srinivasakannan
author_facet Chandralekha, Kuppan
Sureshbabu, Adukamparai Rajukrishnan
Gavaskar, Deivasigamani
Lakshmi, Srinivasakannan
author_sort Chandralekha, Kuppan
collection PubMed
description In the title compound, C(35)H(30)N(4)O(3), the spiro C atom connects the five-membered pyrrolidine ring and the indeno­quinoxaline ring system. The pyrrolidine ring adopts a twist conformation. An intra­molecular N—H⋯N inter­action between the amino group and the pyrazine ring is observed. In the crystal, mol­ecules are linked by a pairs of C—H⋯O hydrogen bonds, forming inversion dimers.
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spelling pubmed-51207012016-12-05 Crystal structure of methyl 3′-benzamido-4′-(4-meth­oxy­phen­yl)-1′-methyl­spiro­[indeno­[1,2-b]quinoxaline-11,2′-pyrrolidine]-3′-carboxyl­ate Chandralekha, Kuppan Sureshbabu, Adukamparai Rajukrishnan Gavaskar, Deivasigamani Lakshmi, Srinivasakannan Acta Crystallogr E Crystallogr Commun Research Communications In the title compound, C(35)H(30)N(4)O(3), the spiro C atom connects the five-membered pyrrolidine ring and the indeno­quinoxaline ring system. The pyrrolidine ring adopts a twist conformation. An intra­molecular N—H⋯N inter­action between the amino group and the pyrazine ring is observed. In the crystal, mol­ecules are linked by a pairs of C—H⋯O hydrogen bonds, forming inversion dimers. International Union of Crystallography 2016-08-05 /pmc/articles/PMC5120701/ /pubmed/27920911 http://dx.doi.org/10.1107/S2056989016012469 Text en © Chandralekha et al. 2016 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 Research Communications
Chandralekha, Kuppan
Sureshbabu, Adukamparai Rajukrishnan
Gavaskar, Deivasigamani
Lakshmi, Srinivasakannan
Crystal structure of methyl 3′-benzamido-4′-(4-meth­oxy­phen­yl)-1′-methyl­spiro­[indeno­[1,2-b]quinoxaline-11,2′-pyrrolidine]-3′-carboxyl­ate
title Crystal structure of methyl 3′-benzamido-4′-(4-meth­oxy­phen­yl)-1′-methyl­spiro­[indeno­[1,2-b]quinoxaline-11,2′-pyrrolidine]-3′-carboxyl­ate
title_full Crystal structure of methyl 3′-benzamido-4′-(4-meth­oxy­phen­yl)-1′-methyl­spiro­[indeno­[1,2-b]quinoxaline-11,2′-pyrrolidine]-3′-carboxyl­ate
title_fullStr Crystal structure of methyl 3′-benzamido-4′-(4-meth­oxy­phen­yl)-1′-methyl­spiro­[indeno­[1,2-b]quinoxaline-11,2′-pyrrolidine]-3′-carboxyl­ate
title_full_unstemmed Crystal structure of methyl 3′-benzamido-4′-(4-meth­oxy­phen­yl)-1′-methyl­spiro­[indeno­[1,2-b]quinoxaline-11,2′-pyrrolidine]-3′-carboxyl­ate
title_short Crystal structure of methyl 3′-benzamido-4′-(4-meth­oxy­phen­yl)-1′-methyl­spiro­[indeno­[1,2-b]quinoxaline-11,2′-pyrrolidine]-3′-carboxyl­ate
title_sort crystal structure of methyl 3′-benzamido-4′-(4-meth­oxy­phen­yl)-1′-methyl­spiro­[indeno­[1,2-b]quinoxaline-11,2′-pyrrolidine]-3′-carboxyl­ate
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120701/
https://www.ncbi.nlm.nih.gov/pubmed/27920911
http://dx.doi.org/10.1107/S2056989016012469
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