Cyclo­hexa­nespiro-2′-[2′,3′,6′,7′-tetra­hydro-1′H-cyclo­penta­[d]pyrimidin]-4′(5′H)-one

The title compound, C(12)H(18)N(2)O, was synthesized by the reaction of cyclo­hexa­none and 2-amino­cyclo­pent-1-enecarbonitrile. In the mol­ecule of the title compound, the six-carbon ring displays a chair conformation, the six-membered 1,3-diaza ring and the cyclo­pentene ring both assume envelope...

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Detalles Bibliográficos
Autores principales: Shi, Daxin, Qian, Dongfeng, Zhang, Qi, Li, Jiarong
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968495/
https://www.ncbi.nlm.nih.gov/pubmed/21582267
http://dx.doi.org/10.1107/S1600536809005388
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author Shi, Daxin
Qian, Dongfeng
Zhang, Qi
Li, Jiarong
author_facet Shi, Daxin
Qian, Dongfeng
Zhang, Qi
Li, Jiarong
author_sort Shi, Daxin
collection PubMed
description The title compound, C(12)H(18)N(2)O, was synthesized by the reaction of cyclo­hexa­none and 2-amino­cyclo­pent-1-enecarbonitrile. In the mol­ecule of the title compound, the six-carbon ring displays a chair conformation, the six-membered 1,3-diaza ring and the cyclo­pentene ring both assume envelope conformations. Supra­molecular aggregation is achieved by N—H⋯O hydrogen bonds.
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spelling pubmed-29684952010-12-30 Cyclo­hexa­nespiro-2′-[2′,3′,6′,7′-tetra­hydro-1′H-cyclo­penta­[d]pyrimidin]-4′(5′H)-one Shi, Daxin Qian, Dongfeng Zhang, Qi Li, Jiarong Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(12)H(18)N(2)O, was synthesized by the reaction of cyclo­hexa­none and 2-amino­cyclo­pent-1-enecarbonitrile. In the mol­ecule of the title compound, the six-carbon ring displays a chair conformation, the six-membered 1,3-diaza ring and the cyclo­pentene ring both assume envelope conformations. Supra­molecular aggregation is achieved by N—H⋯O hydrogen bonds. International Union of Crystallography 2009-02-28 /pmc/articles/PMC2968495/ /pubmed/21582267 http://dx.doi.org/10.1107/S1600536809005388 Text en © Shi 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
Shi, Daxin
Qian, Dongfeng
Zhang, Qi
Li, Jiarong
Cyclo­hexa­nespiro-2′-[2′,3′,6′,7′-tetra­hydro-1′H-cyclo­penta­[d]pyrimidin]-4′(5′H)-one
title Cyclo­hexa­nespiro-2′-[2′,3′,6′,7′-tetra­hydro-1′H-cyclo­penta­[d]pyrimidin]-4′(5′H)-one
title_full Cyclo­hexa­nespiro-2′-[2′,3′,6′,7′-tetra­hydro-1′H-cyclo­penta­[d]pyrimidin]-4′(5′H)-one
title_fullStr Cyclo­hexa­nespiro-2′-[2′,3′,6′,7′-tetra­hydro-1′H-cyclo­penta­[d]pyrimidin]-4′(5′H)-one
title_full_unstemmed Cyclo­hexa­nespiro-2′-[2′,3′,6′,7′-tetra­hydro-1′H-cyclo­penta­[d]pyrimidin]-4′(5′H)-one
title_short Cyclo­hexa­nespiro-2′-[2′,3′,6′,7′-tetra­hydro-1′H-cyclo­penta­[d]pyrimidin]-4′(5′H)-one
title_sort cyclo­hexa­nespiro-2′-[2′,3′,6′,7′-tetra­hydro-1′h-cyclo­penta­[d]pyrimidin]-4′(5′h)-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968495/
https://www.ncbi.nlm.nih.gov/pubmed/21582267
http://dx.doi.org/10.1107/S1600536809005388
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AT qiandongfeng cyclohexanespiro22367tetrahydro1hcyclopentadpyrimidin45hone
AT zhangqi cyclohexanespiro22367tetrahydro1hcyclopentadpyrimidin45hone
AT lijiarong cyclohexanespiro22367tetrahydro1hcyclopentadpyrimidin45hone

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