Synthesis and X-ray diffraction data of 1-N-(3-pyridylmethyl) aminonaphthalene hydrochloride
dc.contributor.author | Morantes, L.R. | spa |
dc.contributor.author | Medina, C.F. | spa |
dc.contributor.author | Henao, J.A. | spa |
dc.contributor.author | Kouznetsov, V.V. | spa |
dc.contributor.author | Camargo, H.A. | spa |
dc.coverage.campus | CRAI-USTA Bogotá | spa |
dc.date.accessioned | 2020-01-17T15:13:53Z | spa |
dc.date.available | 2020-01-17T15:13:53Z | spa |
dc.date.issued | 2014-06 | spa |
dc.description.abstract | The 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.domain | http://unidadinvestigacion.usta.edu.co | spa |
dc.format.mimetype | application/pdf | spa |
dc.identifier.doi | https://doi.org/10.1017/S0885715614000049 | spa |
dc.identifier.uri | http://hdl.handle.net/11634/20692 | |
dc.relation.references | Boultif, 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.references | Buhrke, 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.references | Camargo, 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.references | Camargo, 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.references | de Wolff, P. M. (1968). “A simplified criterion for the reliability of a powder pattern indexing,” J. Appl. Crystallogr. 1, 108–113. | spa |
dc.relation.references | Dong, C. (1999). “PowderX: Windows-95-based program for powder X-ray diffraction data processing,” J. Appl. Crystallogr. 32, 838. | spa |
dc.relation.references | Graham, T. W. and Fryhte, G. B. (2011). The Chemistry of Biologically Important Amines (Wiley, México), Vol. 10, pp. 922–924. | spa |
dc.relation.references | Kouznetsov, 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.references | Laugier, 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.references | Miguell, 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.references | Rachinger, 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.references | Saviztky, A. and Golay, M. J. (1964) “Smoothing and differentiation of data by simplified least squares procedures,” Anal. Chem. 36, 1627–1639. | spa |
dc.relation.references | Schäfer-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.references | Serajuddin, A. (2007). “Salt formation to improve drug solubility,” Adv. Drug Deliv. Rev. 59, 603–616. | spa |
dc.relation.references | Smith, 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.references | Sonneveld, E. J. and Visser, J. W. (1975). “Automatic collection of powder diffraction data from photographs,” J. Appl. Crystallogr. 8, 1–7. | spa |
dc.relation.references | Vargas, 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.rights | Atribución-NoComercial-CompartirIgual 2.5 Colombia | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/2.5/co/ | * |
dc.subject.keyword | Derivatization | spa |
dc.subject.keyword | X-ray powder diffraction | spa |
dc.subject.keyword | 1-naphthalene ammonium salt | spa |
dc.title | Synthesis and X-ray diffraction data of 1-N-(3-pyridylmethyl) aminonaphthalene hydrochloride | spa |
dc.type.category | Generación de Nuevo Conocimiento: Artículos publicados en revistas especializadas - Electrónicos | spa |
Archivos
Bloque original
1 - 1 de 1
Cargando...
- Nombre:
- Synthesis and X-ray diffraction data of 1-N-(3-pyridylmethyl) aminonaphthalene hydrochloride.pdf
- Tamaño:
- 108.75 KB
- Formato:
- Adobe Portable Document Format
- Descripción:
- Artículo SCOPUS
Bloque de licencias
1 - 1 de 1

- Nombre:
- license.txt
- Tamaño:
- 807 B
- Formato:
- Item-specific license agreed upon to submission
- Descripción: