Ethyl 3-bromo-1-(3-chloro­pyridin-2-yl)-1H-pyrazole-5-carboxyl­ate

The title compound, C(11)H(9)BrClN(3)O(2), is an inter­mediate in the synthesis of Rynaxypyre, a new insecticidal anthranilic diamide used as a potent and selective ryanodine receptor activator. The dihedral angle between the aromatic ring planes is 78.7 (2)°.

Detalles Bibliográficos
Autores principales: He, Hai-Bing, Liu, Shan, Tan, Hai-Jun, Xia, Ming, Zhu, Hong-Jun
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968002/
https://www.ncbi.nlm.nih.gov/pubmed/21581733
http://dx.doi.org/10.1107/S1600536808039329
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author He, Hai-Bing
Liu, Shan
Tan, Hai-Jun
Xia, Ming
Zhu, Hong-Jun
author_facet He, Hai-Bing
Liu, Shan
Tan, Hai-Jun
Xia, Ming
Zhu, Hong-Jun
author_sort He, Hai-Bing
collection PubMed
description The title compound, C(11)H(9)BrClN(3)O(2), is an inter­mediate in the synthesis of Rynaxypyre, a new insecticidal anthranilic diamide used as a potent and selective ryanodine receptor activator. The dihedral angle between the aromatic ring planes is 78.7 (2)°.
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spelling pubmed-29680022010-12-30 Ethyl 3-bromo-1-(3-chloro­pyridin-2-yl)-1H-pyrazole-5-carboxyl­ate He, Hai-Bing Liu, Shan Tan, Hai-Jun Xia, Ming Zhu, Hong-Jun Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(11)H(9)BrClN(3)O(2), is an inter­mediate in the synthesis of Rynaxypyre, a new insecticidal anthranilic diamide used as a potent and selective ryanodine receptor activator. The dihedral angle between the aromatic ring planes is 78.7 (2)°. International Union of Crystallography 2008-12-13 /pmc/articles/PMC2968002/ /pubmed/21581733 http://dx.doi.org/10.1107/S1600536808039329 Text en © He et al. 2009 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
He, Hai-Bing
Liu, Shan
Tan, Hai-Jun
Xia, Ming
Zhu, Hong-Jun
Ethyl 3-bromo-1-(3-chloro­pyridin-2-yl)-1H-pyrazole-5-carboxyl­ate
title Ethyl 3-bromo-1-(3-chloro­pyridin-2-yl)-1H-pyrazole-5-carboxyl­ate
title_full Ethyl 3-bromo-1-(3-chloro­pyridin-2-yl)-1H-pyrazole-5-carboxyl­ate
title_fullStr Ethyl 3-bromo-1-(3-chloro­pyridin-2-yl)-1H-pyrazole-5-carboxyl­ate
title_full_unstemmed Ethyl 3-bromo-1-(3-chloro­pyridin-2-yl)-1H-pyrazole-5-carboxyl­ate
title_short Ethyl 3-bromo-1-(3-chloro­pyridin-2-yl)-1H-pyrazole-5-carboxyl­ate
title_sort ethyl 3-bromo-1-(3-chloro­pyridin-2-yl)-1h-pyrazole-5-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968002/
https://www.ncbi.nlm.nih.gov/pubmed/21581733
http://dx.doi.org/10.1107/S1600536808039329
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AT xiaming ethyl3bromo13chloropyridin2yl1hpyrazole5carboxylate
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