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Ethyl 1-(4-methoxy­phen­yl)-2-nitro-3-[4-oxo-3-phenyl-1-(4-methoxy­phen­yl)azetidin-2-yl]-2,3,10,10a-tetra­hydro-1H,5H-pyrrolo[1,2-b]isoquinoline-10a-carboxyl­ate

In the mol­ecule of the title compound, C(38)H(37)N(3)O(7), the pyrrolidine ring adopts a twist conformation and the six-membered heterocyclic ring has a boat conformation. In the crystal structure, mol­ecules are linked into a three-dimensional framework through inter­molecular C—H⋯O hydrogen bonds...

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Detalles Bibliográficos
Autores principales: Kamala, E. Theboral Sugi, Nirmala, S., Sudha, L., Arumugam, N., Raghunathan, R.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961124/
https://www.ncbi.nlm.nih.gov/pubmed/21202371
http://dx.doi.org/10.1107/S1600536808010428
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author Kamala, E. Theboral Sugi
Nirmala, S.
Sudha, L.
Arumugam, N.
Raghunathan, R.
author_facet Kamala, E. Theboral Sugi
Nirmala, S.
Sudha, L.
Arumugam, N.
Raghunathan, R.
author_sort Kamala, E. Theboral Sugi
collection PubMed
description In the mol­ecule of the title compound, C(38)H(37)N(3)O(7), the pyrrolidine ring adopts a twist conformation and the six-membered heterocyclic ring has a boat conformation. In the crystal structure, mol­ecules are linked into a three-dimensional framework through inter­molecular C—H⋯O hydrogen bonds. One ethyl group is disordered over two positions with occupancies 0.67 (2)/0.33 (2).
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spelling pubmed-29611242010-12-30 Ethyl 1-(4-methoxy­phen­yl)-2-nitro-3-[4-oxo-3-phenyl-1-(4-methoxy­phen­yl)azetidin-2-yl]-2,3,10,10a-tetra­hydro-1H,5H-pyrrolo[1,2-b]isoquinoline-10a-carboxyl­ate Kamala, E. Theboral Sugi Nirmala, S. Sudha, L. Arumugam, N. Raghunathan, R. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the mol­ecule of the title compound, C(38)H(37)N(3)O(7), the pyrrolidine ring adopts a twist conformation and the six-membered heterocyclic ring has a boat conformation. In the crystal structure, mol­ecules are linked into a three-dimensional framework through inter­molecular C—H⋯O hydrogen bonds. One ethyl group is disordered over two positions with occupancies 0.67 (2)/0.33 (2). International Union of Crystallography 2008-04-23 /pmc/articles/PMC2961124/ /pubmed/21202371 http://dx.doi.org/10.1107/S1600536808010428 Text en © Kamala 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
Kamala, E. Theboral Sugi
Nirmala, S.
Sudha, L.
Arumugam, N.
Raghunathan, R.
Ethyl 1-(4-methoxy­phen­yl)-2-nitro-3-[4-oxo-3-phenyl-1-(4-methoxy­phen­yl)azetidin-2-yl]-2,3,10,10a-tetra­hydro-1H,5H-pyrrolo[1,2-b]isoquinoline-10a-carboxyl­ate
title Ethyl 1-(4-methoxy­phen­yl)-2-nitro-3-[4-oxo-3-phenyl-1-(4-methoxy­phen­yl)azetidin-2-yl]-2,3,10,10a-tetra­hydro-1H,5H-pyrrolo[1,2-b]isoquinoline-10a-carboxyl­ate
title_full Ethyl 1-(4-methoxy­phen­yl)-2-nitro-3-[4-oxo-3-phenyl-1-(4-methoxy­phen­yl)azetidin-2-yl]-2,3,10,10a-tetra­hydro-1H,5H-pyrrolo[1,2-b]isoquinoline-10a-carboxyl­ate
title_fullStr Ethyl 1-(4-methoxy­phen­yl)-2-nitro-3-[4-oxo-3-phenyl-1-(4-methoxy­phen­yl)azetidin-2-yl]-2,3,10,10a-tetra­hydro-1H,5H-pyrrolo[1,2-b]isoquinoline-10a-carboxyl­ate
title_full_unstemmed Ethyl 1-(4-methoxy­phen­yl)-2-nitro-3-[4-oxo-3-phenyl-1-(4-methoxy­phen­yl)azetidin-2-yl]-2,3,10,10a-tetra­hydro-1H,5H-pyrrolo[1,2-b]isoquinoline-10a-carboxyl­ate
title_short Ethyl 1-(4-methoxy­phen­yl)-2-nitro-3-[4-oxo-3-phenyl-1-(4-methoxy­phen­yl)azetidin-2-yl]-2,3,10,10a-tetra­hydro-1H,5H-pyrrolo[1,2-b]isoquinoline-10a-carboxyl­ate
title_sort ethyl 1-(4-methoxy­phen­yl)-2-nitro-3-[4-oxo-3-phenyl-1-(4-methoxy­phen­yl)azetidin-2-yl]-2,3,10,10a-tetra­hydro-1h,5h-pyrrolo[1,2-b]isoquinoline-10a-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961124/
https://www.ncbi.nlm.nih.gov/pubmed/21202371
http://dx.doi.org/10.1107/S1600536808010428
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