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Diphenyl [(S)-1-phenylpropanamido]phosphate
The title compound, C(21)H(22)NO(3)P, was synthesized from the reaction of (C(6)H(5)O)(2)P(O)(Cl) and S-1-phenylpropylamine (1:2 mole ratio) at 273 K, followed by removal of the S-1-phenylpropylamine hydrochloride by-product by dissolving in H(2)O. The P atom is located in a distorted tetrahed...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200690/ https://www.ncbi.nlm.nih.gov/pubmed/22064755 http://dx.doi.org/10.1107/S1600536811034507 |
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author | Sabbaghi, Fahimeh Pourayoubi, Mehrdad Negari, Monireh Nečas, Marek |
author_facet | Sabbaghi, Fahimeh Pourayoubi, Mehrdad Negari, Monireh Nečas, Marek |
author_sort | Sabbaghi, Fahimeh |
collection | PubMed |
description | The title compound, C(21)H(22)NO(3)P, was synthesized from the reaction of (C(6)H(5)O)(2)P(O)(Cl) and S-1-phenylpropylamine (1:2 mole ratio) at 273 K, followed by removal of the S-1-phenylpropylamine hydrochloride by-product by dissolving in H(2)O. The P atom is located in a distorted tetrahedral environment. The bond angles at the P atom vary from 99.51 (12) to 116.68 (12)°. The sp (2) character of the N atom is reflected by the C—N—P angle [120.9 (2)°]. The P=O group and the N—H unit adopt an anti orientation with respect to one another. In the crystal, adjacent molecules are linked via N—H⋯O(P) hydrogen bonds into a one-dimensional arrangement running parallel to the a axis. |
format | Online Article Text |
id | pubmed-3200690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32006902011-11-06 Diphenyl [(S)-1-phenylpropanamido]phosphate Sabbaghi, Fahimeh Pourayoubi, Mehrdad Negari, Monireh Nečas, Marek Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(21)H(22)NO(3)P, was synthesized from the reaction of (C(6)H(5)O)(2)P(O)(Cl) and S-1-phenylpropylamine (1:2 mole ratio) at 273 K, followed by removal of the S-1-phenylpropylamine hydrochloride by-product by dissolving in H(2)O. The P atom is located in a distorted tetrahedral environment. The bond angles at the P atom vary from 99.51 (12) to 116.68 (12)°. The sp (2) character of the N atom is reflected by the C—N—P angle [120.9 (2)°]. The P=O group and the N—H unit adopt an anti orientation with respect to one another. In the crystal, adjacent molecules are linked via N—H⋯O(P) hydrogen bonds into a one-dimensional arrangement running parallel to the a axis. International Union of Crystallography 2011-08-27 /pmc/articles/PMC3200690/ /pubmed/22064755 http://dx.doi.org/10.1107/S1600536811034507 Text en © Sabbaghi et al. 2011 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 Sabbaghi, Fahimeh Pourayoubi, Mehrdad Negari, Monireh Nečas, Marek Diphenyl [(S)-1-phenylpropanamido]phosphate |
title | Diphenyl [(S)-1-phenylpropanamido]phosphate |
title_full | Diphenyl [(S)-1-phenylpropanamido]phosphate |
title_fullStr | Diphenyl [(S)-1-phenylpropanamido]phosphate |
title_full_unstemmed | Diphenyl [(S)-1-phenylpropanamido]phosphate |
title_short | Diphenyl [(S)-1-phenylpropanamido]phosphate |
title_sort | diphenyl [(s)-1-phenylpropanamido]phosphate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200690/ https://www.ncbi.nlm.nih.gov/pubmed/22064755 http://dx.doi.org/10.1107/S1600536811034507 |
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