Spiro­[cyclo­pentane-1,2′(1′H)-pyrido[2,3-d]pyrimidin]-4′(3′H)-one

The title compound, C(11)H(13)N(2)O, was obtained by cyclo­condensation of 2-amino­pyridine-3-carbonitrile with cyclo­penta­none. The mol­ecule is built up from two fused six-membered rings and one five-membered ring linked through a spiro C atom. Both the pyrimidine and the cyclo­pentane rings adop...

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Detalles Bibliográficos
Autores principales: Shi, Daxin, Yang, Liupan, Tang, Jianhong, Wang, Xiuzhen, Li, Jiarong
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3008029/
https://www.ncbi.nlm.nih.gov/pubmed/21588651
http://dx.doi.org/10.1107/S1600536810027479
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author Shi, Daxin
Yang, Liupan
Tang, Jianhong
Wang, Xiuzhen
Li, Jiarong
author_facet Shi, Daxin
Yang, Liupan
Tang, Jianhong
Wang, Xiuzhen
Li, Jiarong
author_sort Shi, Daxin
collection PubMed
description The title compound, C(11)H(13)N(2)O, was obtained by cyclo­condensation of 2-amino­pyridine-3-carbonitrile with cyclo­penta­none. The mol­ecule is built up from two fused six-membered rings and one five-membered ring linked through a spiro C atom. Both the pyrimidine and the cyclo­pentane rings adopt envelope conformations. In the crystal structure, mol­ecules are linked by inter­molecular N—H⋯O hydrogen bonds.
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spelling pubmed-30080292010-12-30 Spiro­[cyclo­pentane-1,2′(1′H)-pyrido[2,3-d]pyrimidin]-4′(3′H)-one Shi, Daxin Yang, Liupan Tang, Jianhong Wang, Xiuzhen Li, Jiarong Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(11)H(13)N(2)O, was obtained by cyclo­condensation of 2-amino­pyridine-3-carbonitrile with cyclo­penta­none. The mol­ecule is built up from two fused six-membered rings and one five-membered ring linked through a spiro C atom. Both the pyrimidine and the cyclo­pentane rings adopt envelope conformations. In the crystal structure, mol­ecules are linked by inter­molecular N—H⋯O hydrogen bonds. International Union of Crystallography 2010-08-18 /pmc/articles/PMC3008029/ /pubmed/21588651 http://dx.doi.org/10.1107/S1600536810027479 Text en © Shi et al. 2010 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
Yang, Liupan
Tang, Jianhong
Wang, Xiuzhen
Li, Jiarong
Spiro­[cyclo­pentane-1,2′(1′H)-pyrido[2,3-d]pyrimidin]-4′(3′H)-one
title Spiro­[cyclo­pentane-1,2′(1′H)-pyrido[2,3-d]pyrimidin]-4′(3′H)-one
title_full Spiro­[cyclo­pentane-1,2′(1′H)-pyrido[2,3-d]pyrimidin]-4′(3′H)-one
title_fullStr Spiro­[cyclo­pentane-1,2′(1′H)-pyrido[2,3-d]pyrimidin]-4′(3′H)-one
title_full_unstemmed Spiro­[cyclo­pentane-1,2′(1′H)-pyrido[2,3-d]pyrimidin]-4′(3′H)-one
title_short Spiro­[cyclo­pentane-1,2′(1′H)-pyrido[2,3-d]pyrimidin]-4′(3′H)-one
title_sort spiro­[cyclo­pentane-1,2′(1′h)-pyrido[2,3-d]pyrimidin]-4′(3′h)-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3008029/
https://www.ncbi.nlm.nih.gov/pubmed/21588651
http://dx.doi.org/10.1107/S1600536810027479
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AT tangjianhong spirocyclopentane121hpyrido23dpyrimidin43hone
AT wangxiuzhen spirocyclopentane121hpyrido23dpyrimidin43hone
AT lijiarong spirocyclopentane121hpyrido23dpyrimidin43hone

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