1,3,3-Trimethyl-1,2,3,4-tetra­hydro­pyrido[1,2-a]benzimidazol-1-ol

In the title compound, C(14)H(18)N(2)O, the benzimidazole grouping is close to planar, with a maximum deviation of 0.042 Å; the six-membered non-aromatic ring adopts an envelope conformation. In the crystal structure, mol­ecules are linked into infinite sheets lying parallel to the bc plane by O—H⋯N...

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Autores principales: Mehdi, Sayed Hasan, Hashim, Rokiah, Ghalib, Raza Murad, Yeap, Chin Sing, Fun, Hoong-Kun
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006987/
https://www.ncbi.nlm.nih.gov/pubmed/21588036
http://dx.doi.org/10.1107/S1600536810024487
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author Mehdi, Sayed Hasan
Hashim, Rokiah
Ghalib, Raza Murad
Yeap, Chin Sing
Fun, Hoong-Kun
author_facet Mehdi, Sayed Hasan
Hashim, Rokiah
Ghalib, Raza Murad
Yeap, Chin Sing
Fun, Hoong-Kun
author_sort Mehdi, Sayed Hasan
collection PubMed
description In the title compound, C(14)H(18)N(2)O, the benzimidazole grouping is close to planar, with a maximum deviation of 0.042 Å; the six-membered non-aromatic ring adopts an envelope conformation. In the crystal structure, mol­ecules are linked into infinite sheets lying parallel to the bc plane by O—H⋯N and C—H⋯O hydrogen bonds.
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spelling pubmed-30069872010-12-30 1,3,3-Trimethyl-1,2,3,4-tetra­hydro­pyrido[1,2-a]benzimidazol-1-ol Mehdi, Sayed Hasan Hashim, Rokiah Ghalib, Raza Murad Yeap, Chin Sing Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(14)H(18)N(2)O, the benzimidazole grouping is close to planar, with a maximum deviation of 0.042 Å; the six-membered non-aromatic ring adopts an envelope conformation. In the crystal structure, mol­ecules are linked into infinite sheets lying parallel to the bc plane by O—H⋯N and C—H⋯O hydrogen bonds. International Union of Crystallography 2010-06-26 /pmc/articles/PMC3006987/ /pubmed/21588036 http://dx.doi.org/10.1107/S1600536810024487 Text en © Mehdi 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
Mehdi, Sayed Hasan
Hashim, Rokiah
Ghalib, Raza Murad
Yeap, Chin Sing
Fun, Hoong-Kun
1,3,3-Trimethyl-1,2,3,4-tetra­hydro­pyrido[1,2-a]benzimidazol-1-ol
title 1,3,3-Trimethyl-1,2,3,4-tetra­hydro­pyrido[1,2-a]benzimidazol-1-ol
title_full 1,3,3-Trimethyl-1,2,3,4-tetra­hydro­pyrido[1,2-a]benzimidazol-1-ol
title_fullStr 1,3,3-Trimethyl-1,2,3,4-tetra­hydro­pyrido[1,2-a]benzimidazol-1-ol
title_full_unstemmed 1,3,3-Trimethyl-1,2,3,4-tetra­hydro­pyrido[1,2-a]benzimidazol-1-ol
title_short 1,3,3-Trimethyl-1,2,3,4-tetra­hydro­pyrido[1,2-a]benzimidazol-1-ol
title_sort 1,3,3-trimethyl-1,2,3,4-tetra­hydro­pyrido[1,2-a]benzimidazol-1-ol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006987/
https://www.ncbi.nlm.nih.gov/pubmed/21588036
http://dx.doi.org/10.1107/S1600536810024487
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