1-Isobutyl-N,N-dimethyl-1H-imidazo[4,5-c]quinolin-4-amine

In the title compound, C(16)H(20)N(4), the 1H-imidazo[4,5-c]quinoline ring system is approximately planar, with a maximum deviation of 0.0719 (15) Å. An intra­molecular C—H⋯N hydrogen bond contributes to the stabilization of the mol­ecule, forming an S(6) ring motif. In the crystal, the mol­ecules a...

Descripción completa

Detalles Bibliográficos
Autores principales: Loh, Wan-Sin, Fun, Hoong-Kun, Kayarmar, Reshma, Viveka, S., Nagaraja, G. K.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051498/
https://www.ncbi.nlm.nih.gov/pubmed/21523077
http://dx.doi.org/10.1107/S160053681100153X
_version_ 1782199493294292992
author Loh, Wan-Sin
Fun, Hoong-Kun
Kayarmar, Reshma
Viveka, S.
Nagaraja, G. K.
author_facet Loh, Wan-Sin
Fun, Hoong-Kun
Kayarmar, Reshma
Viveka, S.
Nagaraja, G. K.
author_sort Loh, Wan-Sin
collection PubMed
description In the title compound, C(16)H(20)N(4), the 1H-imidazo[4,5-c]quinoline ring system is approximately planar, with a maximum deviation of 0.0719 (15) Å. An intra­molecular C—H⋯N hydrogen bond contributes to the stabilization of the mol­ecule, forming an S(6) ring motif. In the crystal, the mol­ecules are stacked along the b axis through weak aromatic π–π inter­actions between benzene and imidazole and benzene and pyridine rings [centroid–centroid distances = 3.6055 (10) and 3.5342 (10) Å, respectively].
format Text
id pubmed-3051498
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-30514982011-04-26 1-Isobutyl-N,N-dimethyl-1H-imidazo[4,5-c]quinolin-4-amine Loh, Wan-Sin Fun, Hoong-Kun Kayarmar, Reshma Viveka, S. Nagaraja, G. K. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(20)N(4), the 1H-imidazo[4,5-c]quinoline ring system is approximately planar, with a maximum deviation of 0.0719 (15) Å. An intra­molecular C—H⋯N hydrogen bond contributes to the stabilization of the mol­ecule, forming an S(6) ring motif. In the crystal, the mol­ecules are stacked along the b axis through weak aromatic π–π inter­actions between benzene and imidazole and benzene and pyridine rings [centroid–centroid distances = 3.6055 (10) and 3.5342 (10) Å, respectively]. International Union of Crystallography 2011-01-15 /pmc/articles/PMC3051498/ /pubmed/21523077 http://dx.doi.org/10.1107/S160053681100153X Text en © Loh et al. 2011 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
Loh, Wan-Sin
Fun, Hoong-Kun
Kayarmar, Reshma
Viveka, S.
Nagaraja, G. K.
1-Isobutyl-N,N-dimethyl-1H-imidazo[4,5-c]quinolin-4-amine
title 1-Isobutyl-N,N-dimethyl-1H-imidazo[4,5-c]quinolin-4-amine
title_full 1-Isobutyl-N,N-dimethyl-1H-imidazo[4,5-c]quinolin-4-amine
title_fullStr 1-Isobutyl-N,N-dimethyl-1H-imidazo[4,5-c]quinolin-4-amine
title_full_unstemmed 1-Isobutyl-N,N-dimethyl-1H-imidazo[4,5-c]quinolin-4-amine
title_short 1-Isobutyl-N,N-dimethyl-1H-imidazo[4,5-c]quinolin-4-amine
title_sort 1-isobutyl-n,n-dimethyl-1h-imidazo[4,5-c]quinolin-4-amine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051498/
https://www.ncbi.nlm.nih.gov/pubmed/21523077
http://dx.doi.org/10.1107/S160053681100153X
work_keys_str_mv AT lohwansin 1isobutylnndimethyl1himidazo45cquinolin4amine
AT funhoongkun 1isobutylnndimethyl1himidazo45cquinolin4amine
AT kayarmarreshma 1isobutylnndimethyl1himidazo45cquinolin4amine
AT vivekas 1isobutylnndimethyl1himidazo45cquinolin4amine
AT nagarajagk 1isobutylnndimethyl1himidazo45cquinolin4amine

Ejemplares similares