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(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...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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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 |
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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
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title_full | (3S,4R)-4-(4-Fluorophenyl)-3-(hydroxymethyl)piperidinium chloride
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title_fullStr | (3S,4R)-4-(4-Fluorophenyl)-3-(hydroxymethyl)piperidinium chloride
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title_full_unstemmed | (3S,4R)-4-(4-Fluorophenyl)-3-(hydroxymethyl)piperidinium chloride
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title_short | (3S,4R)-4-(4-Fluorophenyl)-3-(hydroxymethyl)piperidinium chloride
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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 |
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