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Synthesis and Crystal Structures of N-Substituted Pyrazolines

Four pyrazole compounds, 3-(4-fluorophenyl)-5-phenyl-4,5-dihydro-1H-pyrazole-1-carbaldehyde (1), 5-(4-bromophenyl)-3-(4-fluorophenyl)-4,5-dihydro-1H-pyrazole-1-carbaldehyde (2), 1-[5-(4-chlorophenyl)-3-(4-fluorophenyl)-4,5-dihydro-1H-pyrazol-1-yl]ethanone (3) and 1-[3-(4-fluorophenyl)-5-phenyl-4,5-d...

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Autores principales: Loh, Wan-Sin, Quah, Ching Kheng, Chia, Tze Shyang, Fun, Hoong-Kun, Sapnakumari, Majal, Narayana, Badiadka, Sarojini, Balladka Kunhanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270533/
https://www.ncbi.nlm.nih.gov/pubmed/23429377
http://dx.doi.org/10.3390/molecules18022386
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author Loh, Wan-Sin
Quah, Ching Kheng
Chia, Tze Shyang
Fun, Hoong-Kun
Sapnakumari, Majal
Narayana, Badiadka
Sarojini, Balladka Kunhanna
author_facet Loh, Wan-Sin
Quah, Ching Kheng
Chia, Tze Shyang
Fun, Hoong-Kun
Sapnakumari, Majal
Narayana, Badiadka
Sarojini, Balladka Kunhanna
author_sort Loh, Wan-Sin
collection PubMed
description Four pyrazole compounds, 3-(4-fluorophenyl)-5-phenyl-4,5-dihydro-1H-pyrazole-1-carbaldehyde (1), 5-(4-bromophenyl)-3-(4-fluorophenyl)-4,5-dihydro-1H-pyrazole-1-carbaldehyde (2), 1-[5-(4-chlorophenyl)-3-(4-fluorophenyl)-4,5-dihydro-1H-pyrazol-1-yl]ethanone (3) and 1-[3-(4-fluorophenyl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl]propan-1-one (4), have been prepared by condensing chalcones with hydrazine hydrate in the presence of aliphatic acids, namely formic acid, acetic acid and propionic acid. The structures were characterized by X-ray single crystal structure determination. The dihedral angles formed between the pyrazole and the fluoro-substituted rings are 4.64(7)° in 1, 5.3(4)° in 2 and 4.89(6)° in 3. In 4, the corresponding angles for molecules A and molecules B are 10.53(10)° and 9.78(10)°, respectively.
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spelling pubmed-62705332018-12-14 Synthesis and Crystal Structures of N-Substituted Pyrazolines Loh, Wan-Sin Quah, Ching Kheng Chia, Tze Shyang Fun, Hoong-Kun Sapnakumari, Majal Narayana, Badiadka Sarojini, Balladka Kunhanna Molecules Article Four pyrazole compounds, 3-(4-fluorophenyl)-5-phenyl-4,5-dihydro-1H-pyrazole-1-carbaldehyde (1), 5-(4-bromophenyl)-3-(4-fluorophenyl)-4,5-dihydro-1H-pyrazole-1-carbaldehyde (2), 1-[5-(4-chlorophenyl)-3-(4-fluorophenyl)-4,5-dihydro-1H-pyrazol-1-yl]ethanone (3) and 1-[3-(4-fluorophenyl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl]propan-1-one (4), have been prepared by condensing chalcones with hydrazine hydrate in the presence of aliphatic acids, namely formic acid, acetic acid and propionic acid. The structures were characterized by X-ray single crystal structure determination. The dihedral angles formed between the pyrazole and the fluoro-substituted rings are 4.64(7)° in 1, 5.3(4)° in 2 and 4.89(6)° in 3. In 4, the corresponding angles for molecules A and molecules B are 10.53(10)° and 9.78(10)°, respectively. MDPI 2013-02-20 /pmc/articles/PMC6270533/ /pubmed/23429377 http://dx.doi.org/10.3390/molecules18022386 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Loh, Wan-Sin
Quah, Ching Kheng
Chia, Tze Shyang
Fun, Hoong-Kun
Sapnakumari, Majal
Narayana, Badiadka
Sarojini, Balladka Kunhanna
Synthesis and Crystal Structures of N-Substituted Pyrazolines
title Synthesis and Crystal Structures of N-Substituted Pyrazolines
title_full Synthesis and Crystal Structures of N-Substituted Pyrazolines
title_fullStr Synthesis and Crystal Structures of N-Substituted Pyrazolines
title_full_unstemmed Synthesis and Crystal Structures of N-Substituted Pyrazolines
title_short Synthesis and Crystal Structures of N-Substituted Pyrazolines
title_sort synthesis and crystal structures of n-substituted pyrazolines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270533/
https://www.ncbi.nlm.nih.gov/pubmed/23429377
http://dx.doi.org/10.3390/molecules18022386
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