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1,1′′-Bis(prop-2-en-1-yl)-1,1′′,2,2′′-tetra­hydro­dispiro­[indole-3,7′-[6,9]diaza­tricyclo­[7.3.0.0(2,6)]dodecane-8′,3′′-indole]-2,2′′-dione

The mol­ecule of the title compound, C(30)H(32)N(4)O(2), lies on a twofold rotation axis that passes through the mid-points of the C—C bonds of the piperazine ring, which adopts a chair conformation. The pyrrolidine ring that is fused to the piperazine ring adopts an envelope conformation (in which...

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Autores principales: Al Mamari, Khalil, Ennajih, Hamid, Bouhfid, Rachid, Essassi, El Mokhtar, Ng, Seik Weng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379240/
https://www.ncbi.nlm.nih.gov/pubmed/22719438
http://dx.doi.org/10.1107/S1600536812019216
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author Al Mamari, Khalil
Ennajih, Hamid
Bouhfid, Rachid
Essassi, El Mokhtar
Ng, Seik Weng
author_facet Al Mamari, Khalil
Ennajih, Hamid
Bouhfid, Rachid
Essassi, El Mokhtar
Ng, Seik Weng
author_sort Al Mamari, Khalil
collection PubMed
description The mol­ecule of the title compound, C(30)H(32)N(4)O(2), lies on a twofold rotation axis that passes through the mid-points of the C—C bonds of the piperazine ring, which adopts a chair conformation. The pyrrolidine ring that is fused to the piperazine ring adopts an envelope conformation (in which the N atom represents the flap). The indoline fused-ring system is nearly planar (r.m.s. deviation = 0.044 Å); the two symmetry-related indoline fused-rings systems are aligned at 71.44 (3)°.
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spelling pubmed-33792402012-06-20 1,1′′-Bis(prop-2-en-1-yl)-1,1′′,2,2′′-tetra­hydro­dispiro­[indole-3,7′-[6,9]diaza­tricyclo­[7.3.0.0(2,6)]dodecane-8′,3′′-indole]-2,2′′-dione Al Mamari, Khalil Ennajih, Hamid Bouhfid, Rachid Essassi, El Mokhtar Ng, Seik Weng Acta Crystallogr Sect E Struct Rep Online Organic Papers The mol­ecule of the title compound, C(30)H(32)N(4)O(2), lies on a twofold rotation axis that passes through the mid-points of the C—C bonds of the piperazine ring, which adopts a chair conformation. The pyrrolidine ring that is fused to the piperazine ring adopts an envelope conformation (in which the N atom represents the flap). The indoline fused-ring system is nearly planar (r.m.s. deviation = 0.044 Å); the two symmetry-related indoline fused-rings systems are aligned at 71.44 (3)°. International Union of Crystallography 2012-05-05 /pmc/articles/PMC3379240/ /pubmed/22719438 http://dx.doi.org/10.1107/S1600536812019216 Text en © Al Mamari et al. 2012 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
Al Mamari, Khalil
Ennajih, Hamid
Bouhfid, Rachid
Essassi, El Mokhtar
Ng, Seik Weng
1,1′′-Bis(prop-2-en-1-yl)-1,1′′,2,2′′-tetra­hydro­dispiro­[indole-3,7′-[6,9]diaza­tricyclo­[7.3.0.0(2,6)]dodecane-8′,3′′-indole]-2,2′′-dione
title 1,1′′-Bis(prop-2-en-1-yl)-1,1′′,2,2′′-tetra­hydro­dispiro­[indole-3,7′-[6,9]diaza­tricyclo­[7.3.0.0(2,6)]dodecane-8′,3′′-indole]-2,2′′-dione
title_full 1,1′′-Bis(prop-2-en-1-yl)-1,1′′,2,2′′-tetra­hydro­dispiro­[indole-3,7′-[6,9]diaza­tricyclo­[7.3.0.0(2,6)]dodecane-8′,3′′-indole]-2,2′′-dione
title_fullStr 1,1′′-Bis(prop-2-en-1-yl)-1,1′′,2,2′′-tetra­hydro­dispiro­[indole-3,7′-[6,9]diaza­tricyclo­[7.3.0.0(2,6)]dodecane-8′,3′′-indole]-2,2′′-dione
title_full_unstemmed 1,1′′-Bis(prop-2-en-1-yl)-1,1′′,2,2′′-tetra­hydro­dispiro­[indole-3,7′-[6,9]diaza­tricyclo­[7.3.0.0(2,6)]dodecane-8′,3′′-indole]-2,2′′-dione
title_short 1,1′′-Bis(prop-2-en-1-yl)-1,1′′,2,2′′-tetra­hydro­dispiro­[indole-3,7′-[6,9]diaza­tricyclo­[7.3.0.0(2,6)]dodecane-8′,3′′-indole]-2,2′′-dione
title_sort 1,1′′-bis(prop-2-en-1-yl)-1,1′′,2,2′′-tetra­hydro­dispiro­[indole-3,7′-[6,9]diaza­tricyclo­[7.3.0.0(2,6)]dodecane-8′,3′′-indole]-2,2′′-dione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379240/
https://www.ncbi.nlm.nih.gov/pubmed/22719438
http://dx.doi.org/10.1107/S1600536812019216
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