Synthesis and X-ray diffraction data of 1-N-(3-pyridylmethyl) aminonaphthalene hydrochloride

dc.contributor.authorMorantes, L.R.spa
dc.contributor.authorMedina, C.F.spa
dc.contributor.authorHenao, J.A.spa
dc.contributor.authorKouznetsov, V.V.spa
dc.contributor.authorCamargo, H.A.spa
dc.coverage.campusCRAI-USTA Bogotáspa
dc.date.accessioned2020-01-17T15:13:53Zspa
dc.date.available2020-01-17T15:13:53Zspa
dc.date.issued2014-06spa
dc.description.abstractThe title compound 1-N-(3-pyridylmethyl)aminonaphthalene hydrochloride (C16H15N2Cl) was obtained by a reaction of α-naphthylamine (1) and N-pyridincarboxaldehyde (2) in anhydrous ethanol in the first step. The formed imine (3) was reduced with sodium borohydride in anhydrous methanol to give the product 1-N-(3-pyridylmethyl)aminonaphthalene (4). Finally, the hydrochloride was prepared by addition of a hydrochloric acid–ethyl acetate solution (ratio 1:3) with constant stirring and maintaining the temperature between 0 and 5 °C, obtaining a yellow polycrystalline solid corresponding to the respective derivative (5). The X-ray powder diffraction pattern for the new compound (5) was obtained. The compound (5) crystallizes in a monoclinic system with the space group P21/m (No. 11) and refined unit-cell parameters: a = 16.257 (8) Å, b = 9.236 (7) Å, c = 13.221 (6) Å, β = 94.87° (5), Z = 6, and V = 1978 (1) Å3.spa
dc.description.domainhttp://unidadinvestigacion.usta.edu.cospa
dc.format.mimetypeapplication/pdfspa
dc.identifier.doihttps://doi.org/10.1017/S0885715614000049spa
dc.identifier.urihttp://hdl.handle.net/11634/20692
dc.relation.referencesBoultif, A. and Loüer, D. (2006). “Indexing of powder diffraction patterns of low symmetry lattices by successive dichotomy method,” J. Appl. Crystallogr. 37, 724–731.spa
dc.relation.referencesBuhrke, V., Jenkins, R., and Smith, D. (1998). Preparation of Specimens for X-ray Fluorescence and X-ray Diffraction Analysis (Wiley, New York), pp. 141–142.spa
dc.relation.referencesCamargo, H. A., Henao, J. A., Amado, D. F., and Kouznetsov, V. V. (2010). “Synthesis and X-ray diffraction data of 1-N-4-pyridylmethylamino naphthalene,” Powder Diffr. 25(1), 72–74.spa
dc.relation.referencesCamargo, H. A., Habran, N. M., Henao, J. A., Amado, D. F., and Kouznetsov, V. V. (2011). “Synthesis and X-ray diffraction data of 1-[N-(methyl)- (3,5-dimethylphenylamino)]methylnaphthalene,” Powder Diffr. 26(1), 74–77.spa
dc.relation.referencesde Wolff, P. M. (1968). “A simplified criterion for the reliability of a powder pattern indexing,” J. Appl. Crystallogr. 1, 108–113.spa
dc.relation.referencesDong, C. (1999). “PowderX: Windows-95-based program for powder X-ray diffraction data processing,” J. Appl. Crystallogr. 32, 838.spa
dc.relation.referencesGraham, T. W. and Fryhte, G. B. (2011). The Chemistry of Biologically Important Amines (Wiley, México), Vol. 10, pp. 922–924.spa
dc.relation.referencesKouznetsov, V. V., Vargas, L. Y., Sortino, M., Vásquez, Y., Gupta, M. D., Freile, M., Enriz, R. D., and Zacchino, S. A. (2008). “Antifungal and cytotoxic activities of some N-substituted aniline derivates bearing a hetaryl fragment,” Bioorg. Med. Chem. 16, 794–809.spa
dc.relation.referencesLaugier, J. and Bochu, B. (2002). CHEKCELL. “LMGP-Suite Suite of Programs for the interpretation of X-ray. Experiments”, ENSP/ Laboratoire des Matériaux et du Génie Physique, BP 46. 38042 Saint Martin d’Hères, France. http://www.inpg.fr/LMGP and http://www. ccp14.ac.uk/tutorial/lmgp/.spa
dc.relation.referencesMiguell, A. D., Hubbard, C. R., and Stalick, J. K. (1981). NBS* AIDS80: A FORTRAN Program for Crystallographic Data Evaluation (Technical Note 1141). Washington, DC: National Bureau of Standards.spa
dc.relation.referencesRachinger, W. A. (1948). “A correction for the α1 α2 doublet in the measurement of widths of X-ray diffraction lines,” J. Sci. Instrum. 25, 254.spa
dc.relation.referencesSaviztky, A. and Golay, M. J. (1964) “Smoothing and differentiation of data by simplified least squares procedures,” Anal. Chem. 36, 1627–1639.spa
dc.relation.referencesSchäfer-Korting, M. Schoellmann, C., and Korting, H. C. (2008). “Fungicidal activity plus reservoir effect allows short treatment courses with Terbinafine in Tinea Pedis,” Skin Pharmacol. Physiol. 21, 203–210.spa
dc.relation.referencesSerajuddin, A. (2007). “Salt formation to improve drug solubility,” Adv. Drug Deliv. Rev. 59, 603–616.spa
dc.relation.referencesSmith, G. S. and Snyder, R. L. (1979). “FN: A criterion for rating powder diffraction patterns and evaluating the reliability of powder-pattern indexing,” J. Appl. Crystallogr. 12, 60–65.spa
dc.relation.referencesSonneveld, E. J. and Visser, J. W. (1975). “Automatic collection of powder diffraction data from photographs,” J. Appl. Crystallogr. 8, 1–7.spa
dc.relation.referencesVargas, L. Y., Castelli, M. V., Kouznetsov, V. V., Urbina, J. M., López, S. N., Sortino, M., Enriz, R. D., Ribas, J. C., and Zacchino, S. A. (2003). “In vitro antifungal activity of new series of homoallylamines and related compounds with inhibitory properties of the synthesis of fungal cell wall polymers,” Bioorg. Med. Chem. 11, 1531–1550.spa
dc.rightsAtribución-NoComercial-CompartirIgual 2.5 Colombia*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/2.5/co/*
dc.subject.keywordDerivatizationspa
dc.subject.keywordX-ray powder diffractionspa
dc.subject.keyword1-naphthalene ammonium saltspa
dc.titleSynthesis and X-ray diffraction data of 1-N-(3-pyridylmethyl) aminonaphthalene hydrochloridespa
dc.type.categoryGeneración de Nuevo Conocimiento: Artículos publicados en revistas especializadas - Electrónicosspa

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