Cargando…

(3S,4R)-4-(4-Fluoro­phen­yl)-3-(hydroxy­meth­yl)piperidinium chloride

The title compound, C(12)H(17)FNO(+)·Cl(−), is a degradation impurity of paroxetine hydro­chloride hemihydrate (PAXIL), an anti­depressant belonging to the group of drugs called selective serotonin reuptake inhibitors (SSRIs). Similar to the paroxetine hydro­chloride salt with protonation having tak...

Descripción completa

Detalles Bibliográficos
Autores principales: Nirmala, M, Sreekanth, B. R., Vishweshwar, Peddy, Moses Babu, J., Anjaneyulu, Y
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961281/
https://www.ncbi.nlm.nih.gov/pubmed/21202292
http://dx.doi.org/10.1107/S1600536808008593
_version_ 1782188945107320832
author Nirmala, M
Sreekanth, B. R.
Vishweshwar, Peddy
Moses Babu, J.
Anjaneyulu, Y
author_facet Nirmala, M
Sreekanth, B. R.
Vishweshwar, Peddy
Moses Babu, J.
Anjaneyulu, Y
author_sort Nirmala, M
collection PubMed
description The title compound, C(12)H(17)FNO(+)·Cl(−), is a degradation impurity of paroxetine hydro­chloride hemihydrate (PAXIL), an anti­depressant belonging to the group of drugs called selective serotonin reuptake inhibitors (SSRIs). Similar to the paroxetine hydro­chloride salt with protonation having taken place on the basic piperidine ring, the degradation impurity also exists as the hydro­chloride salt. The cyclic six-membered piperidinium ring adopts a chair conformation with the hydroxy­methyl and 4-fluoro­phenyl groups in the equatorial positions. The ions form a tape along the b axis through charge-assisted N(+)—H⋯Cl(−) hydrogen bonds; these tapes are connected by O—H⋯Cl(−) hydrogen bonds along the a axis.
format Text
id pubmed-2961281
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29612812010-12-30 (3S,4R)-4-(4-Fluoro­phen­yl)-3-(hydroxy­meth­yl)piperidinium chloride Nirmala, M Sreekanth, B. R. Vishweshwar, Peddy Moses Babu, J. Anjaneyulu, Y Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(12)H(17)FNO(+)·Cl(−), is a degradation impurity of paroxetine hydro­chloride hemihydrate (PAXIL), an anti­depressant belonging to the group of drugs called selective serotonin reuptake inhibitors (SSRIs). Similar to the paroxetine hydro­chloride salt with protonation having taken place on the basic piperidine ring, the degradation impurity also exists as the hydro­chloride salt. The cyclic six-membered piperidinium ring adopts a chair conformation with the hydroxy­methyl and 4-fluoro­phenyl groups in the equatorial positions. The ions form a tape along the b axis through charge-assisted N(+)—H⋯Cl(−) hydrogen bonds; these tapes are connected by O—H⋯Cl(−) hydrogen bonds along the a axis. International Union of Crystallography 2008-04-04 /pmc/articles/PMC2961281/ /pubmed/21202292 http://dx.doi.org/10.1107/S1600536808008593 Text en © Nirmala 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
Nirmala, M
Sreekanth, B. R.
Vishweshwar, Peddy
Moses Babu, J.
Anjaneyulu, Y
(3S,4R)-4-(4-Fluoro­phen­yl)-3-(hydroxy­meth­yl)piperidinium chloride
title (3S,4R)-4-(4-Fluoro­phen­yl)-3-(hydroxy­meth­yl)piperidinium chloride
title_full (3S,4R)-4-(4-Fluoro­phen­yl)-3-(hydroxy­meth­yl)piperidinium chloride
title_fullStr (3S,4R)-4-(4-Fluoro­phen­yl)-3-(hydroxy­meth­yl)piperidinium chloride
title_full_unstemmed (3S,4R)-4-(4-Fluoro­phen­yl)-3-(hydroxy­meth­yl)piperidinium chloride
title_short (3S,4R)-4-(4-Fluoro­phen­yl)-3-(hydroxy­meth­yl)piperidinium chloride
title_sort (3s,4r)-4-(4-fluoro­phen­yl)-3-(hydroxy­meth­yl)piperidinium chloride
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961281/
https://www.ncbi.nlm.nih.gov/pubmed/21202292
http://dx.doi.org/10.1107/S1600536808008593
work_keys_str_mv AT nirmalam 3s4r44fluorophenyl3hydroxymethylpiperidiniumchloride
AT sreekanthbr 3s4r44fluorophenyl3hydroxymethylpiperidiniumchloride
AT vishweshwarpeddy 3s4r44fluorophenyl3hydroxymethylpiperidiniumchloride
AT mosesbabuj 3s4r44fluorophenyl3hydroxymethylpiperidiniumchloride
AT anjaneyuluy 3s4r44fluorophenyl3hydroxymethylpiperidiniumchloride