(±)-Ethyl 6,7-dimeth­oxy-1-(1H-pyrrol-2-yl)-1,2,3,4-tetra­hydroisoquinoline-2-car­boxyl­ate

In the title compound, C(18)H(22)N(2)O(4), the dihedral angle between the pyrrolyl and quinolinyl fragments is 68.97 (2)°. Two non-classical intra­molecular C—H⋯O hydrogen bonds stabilize the mol­ecular geometry. In the crystal structure, mol­ecules form infinite chains via moderate inter­molecular...

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Detalles Bibliográficos
Autores principales: Nikolova, Rosica Petrova, Kolev, Tsonko, Statkova-Abeghe, Stela M., Shivachev, Boris Lubomirov
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960637/
https://www.ncbi.nlm.nih.gov/pubmed/21201775
http://dx.doi.org/10.1107/S1600536808026020
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author Nikolova, Rosica Petrova
Kolev, Tsonko
Statkova-Abeghe, Stela M.
Shivachev, Boris Lubomirov
author_facet Nikolova, Rosica Petrova
Kolev, Tsonko
Statkova-Abeghe, Stela M.
Shivachev, Boris Lubomirov
author_sort Nikolova, Rosica Petrova
collection PubMed
description In the title compound, C(18)H(22)N(2)O(4), the dihedral angle between the pyrrolyl and quinolinyl fragments is 68.97 (2)°. Two non-classical intra­molecular C—H⋯O hydrogen bonds stabilize the mol­ecular geometry. In the crystal structure, mol­ecules form infinite chains via moderate inter­molecular N—H⋯O(CH(3)) hydrogen bonds.
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spelling pubmed-29606372010-12-30 (±)-Ethyl 6,7-dimeth­oxy-1-(1H-pyrrol-2-yl)-1,2,3,4-tetra­hydroisoquinoline-2-car­boxyl­ate Nikolova, Rosica Petrova Kolev, Tsonko Statkova-Abeghe, Stela M. Shivachev, Boris Lubomirov Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(18)H(22)N(2)O(4), the dihedral angle between the pyrrolyl and quinolinyl fragments is 68.97 (2)°. Two non-classical intra­molecular C—H⋯O hydrogen bonds stabilize the mol­ecular geometry. In the crystal structure, mol­ecules form infinite chains via moderate inter­molecular N—H⋯O(CH(3)) hydrogen bonds. International Union of Crystallography 2008-08-20 /pmc/articles/PMC2960637/ /pubmed/21201775 http://dx.doi.org/10.1107/S1600536808026020 Text en © Nikolova et al. 2008 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
Nikolova, Rosica Petrova
Kolev, Tsonko
Statkova-Abeghe, Stela M.
Shivachev, Boris Lubomirov
(±)-Ethyl 6,7-dimeth­oxy-1-(1H-pyrrol-2-yl)-1,2,3,4-tetra­hydroisoquinoline-2-car­boxyl­ate
title (±)-Ethyl 6,7-dimeth­oxy-1-(1H-pyrrol-2-yl)-1,2,3,4-tetra­hydroisoquinoline-2-car­boxyl­ate
title_full (±)-Ethyl 6,7-dimeth­oxy-1-(1H-pyrrol-2-yl)-1,2,3,4-tetra­hydroisoquinoline-2-car­boxyl­ate
title_fullStr (±)-Ethyl 6,7-dimeth­oxy-1-(1H-pyrrol-2-yl)-1,2,3,4-tetra­hydroisoquinoline-2-car­boxyl­ate
title_full_unstemmed (±)-Ethyl 6,7-dimeth­oxy-1-(1H-pyrrol-2-yl)-1,2,3,4-tetra­hydroisoquinoline-2-car­boxyl­ate
title_short (±)-Ethyl 6,7-dimeth­oxy-1-(1H-pyrrol-2-yl)-1,2,3,4-tetra­hydroisoquinoline-2-car­boxyl­ate
title_sort (±)-ethyl 6,7-dimeth­oxy-1-(1h-pyrrol-2-yl)-1,2,3,4-tetra­hydroisoquinoline-2-car­boxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960637/
https://www.ncbi.nlm.nih.gov/pubmed/21201775
http://dx.doi.org/10.1107/S1600536808026020
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AT statkovaabeghestelam ethyl67dimethoxy11hpyrrol2yl1234tetrahydroisoquinoline2carboxylate
AT shivachevborislubomirov ethyl67dimethoxy11hpyrrol2yl1234tetrahydroisoquinoline2carboxylate

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