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Ethyl 5-methyl­imidazo[1,2-a]pyridine-2-carboxyl­ate

The title compound, C(11)H(12)N(2)O(2), was synthesized from the reaction of 6-methyl­pyridin-2-amine and ethyl 3-bromo-2-oxopropionate. In the mol­ecular structure, the six- and five-membered rings are individually almost planar with r.m.s. deviations of 0.003 and 0.002 Å, respectively. The two rin...

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Detalles Bibliográficos
Autores principales: Yao, Jin-hua, Wang, Lan-fang, Guo, Bing, An, Kang, Guan, Jian-ning
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007311/
https://www.ncbi.nlm.nih.gov/pubmed/21588313
http://dx.doi.org/10.1107/S1600536810026577
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author Yao, Jin-hua
Wang, Lan-fang
Guo, Bing
An, Kang
Guan, Jian-ning
author_facet Yao, Jin-hua
Wang, Lan-fang
Guo, Bing
An, Kang
Guan, Jian-ning
author_sort Yao, Jin-hua
collection PubMed
description The title compound, C(11)H(12)N(2)O(2), was synthesized from the reaction of 6-methyl­pyridin-2-amine and ethyl 3-bromo-2-oxopropionate. In the mol­ecular structure, the six- and five-membered rings are individually almost planar with r.m.s. deviations of 0.003 and 0.002 Å, respectively. The two rings are almost coplanar, the dihedral angle between their planes being 1.4 (3)°. Inter­molecular C—H⋯O and C—H⋯N hydrogen bonds are present in the crystal structure.
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spelling pubmed-30073112010-12-30 Ethyl 5-methyl­imidazo[1,2-a]pyridine-2-carboxyl­ate Yao, Jin-hua Wang, Lan-fang Guo, Bing An, Kang Guan, Jian-ning Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(11)H(12)N(2)O(2), was synthesized from the reaction of 6-methyl­pyridin-2-amine and ethyl 3-bromo-2-oxopropionate. In the mol­ecular structure, the six- and five-membered rings are individually almost planar with r.m.s. deviations of 0.003 and 0.002 Å, respectively. The two rings are almost coplanar, the dihedral angle between their planes being 1.4 (3)°. Inter­molecular C—H⋯O and C—H⋯N hydrogen bonds are present in the crystal structure. International Union of Crystallography 2010-07-14 /pmc/articles/PMC3007311/ /pubmed/21588313 http://dx.doi.org/10.1107/S1600536810026577 Text en © Yao 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
Yao, Jin-hua
Wang, Lan-fang
Guo, Bing
An, Kang
Guan, Jian-ning
Ethyl 5-methyl­imidazo[1,2-a]pyridine-2-carboxyl­ate
title Ethyl 5-methyl­imidazo[1,2-a]pyridine-2-carboxyl­ate
title_full Ethyl 5-methyl­imidazo[1,2-a]pyridine-2-carboxyl­ate
title_fullStr Ethyl 5-methyl­imidazo[1,2-a]pyridine-2-carboxyl­ate
title_full_unstemmed Ethyl 5-methyl­imidazo[1,2-a]pyridine-2-carboxyl­ate
title_short Ethyl 5-methyl­imidazo[1,2-a]pyridine-2-carboxyl­ate
title_sort ethyl 5-methyl­imidazo[1,2-a]pyridine-2-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007311/
https://www.ncbi.nlm.nih.gov/pubmed/21588313
http://dx.doi.org/10.1107/S1600536810026577
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AT ankang ethyl5methylimidazo12apyridine2carboxylate
AT guanjianning ethyl5methylimidazo12apyridine2carboxylate