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1-Isobutyl-4-meth­oxy-1H-imidazo[4,5-c]quinoline

In the title compound, C(15)H(17)N(3)O, the 1H-imidazo[4,5-c]quinoline ring system is approximately planar, with a maximum deviation of 0.036 (1) Å. The C—N—C—C torsion angles formed between this ring system and the isobutyl unit are −99.77 (16) and 79.71 (17)°. In the crystal, inter­molecular C—H⋯O...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Loh, Wan-Sin, Dinesha, Kayarmar, Reshma, Nagaraja, G. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200859/
https://www.ncbi.nlm.nih.gov/pubmed/22058955
http://dx.doi.org/10.1107/S1600536811031801
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author Fun, Hoong-Kun
Loh, Wan-Sin
Dinesha,
Kayarmar, Reshma
Nagaraja, G. K.
author_facet Fun, Hoong-Kun
Loh, Wan-Sin
Dinesha,
Kayarmar, Reshma
Nagaraja, G. K.
author_sort Fun, Hoong-Kun
collection PubMed
description In the title compound, C(15)H(17)N(3)O, the 1H-imidazo[4,5-c]quinoline ring system is approximately planar, with a maximum deviation of 0.036 (1) Å. The C—N—C—C torsion angles formed between this ring system and the isobutyl unit are −99.77 (16) and 79.71 (17)°. In the crystal, inter­molecular C—H⋯O hydrogen bonds link the mol­ecules into chains along the c axis.
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spelling pubmed-32008592011-11-06 1-Isobutyl-4-meth­oxy-1H-imidazo[4,5-c]quinoline Fun, Hoong-Kun Loh, Wan-Sin Dinesha, Kayarmar, Reshma Nagaraja, G. K. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(17)N(3)O, the 1H-imidazo[4,5-c]quinoline ring system is approximately planar, with a maximum deviation of 0.036 (1) Å. The C—N—C—C torsion angles formed between this ring system and the isobutyl unit are −99.77 (16) and 79.71 (17)°. In the crystal, inter­molecular C—H⋯O hydrogen bonds link the mol­ecules into chains along the c axis. International Union of Crystallography 2011-08-11 /pmc/articles/PMC3200859/ /pubmed/22058955 http://dx.doi.org/10.1107/S1600536811031801 Text en © Fun 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
Fun, Hoong-Kun
Loh, Wan-Sin
Dinesha,
Kayarmar, Reshma
Nagaraja, G. K.
1-Isobutyl-4-meth­oxy-1H-imidazo[4,5-c]quinoline
title 1-Isobutyl-4-meth­oxy-1H-imidazo[4,5-c]quinoline
title_full 1-Isobutyl-4-meth­oxy-1H-imidazo[4,5-c]quinoline
title_fullStr 1-Isobutyl-4-meth­oxy-1H-imidazo[4,5-c]quinoline
title_full_unstemmed 1-Isobutyl-4-meth­oxy-1H-imidazo[4,5-c]quinoline
title_short 1-Isobutyl-4-meth­oxy-1H-imidazo[4,5-c]quinoline
title_sort 1-isobutyl-4-meth­oxy-1h-imidazo[4,5-c]quinoline
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200859/
https://www.ncbi.nlm.nih.gov/pubmed/22058955
http://dx.doi.org/10.1107/S1600536811031801
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