How to cite this paper
Sweidan, K., Khanfar, M., Al-Shamaileh, A., Sunjuk, M & Joshi, R. (2019). Synthesis, characterization and crystal structure of pentyl 2-(1H-indole-2-carboxamido)benzoate.Current Chemistry Letters, 8(1), 63-68.
Refrences
1 Kondreddi, R. R., Jiricek, J., Rao, S. P. S., Lakshminarayana, S. B., Camacho, L. R., Rao, R., Herve, M., Bifani, P., Ma, N. L., Kuhen, K., Goh, A., Chatterjee, A. K., Dick, T., Diagana, T. T., Manjunatha, U. H., and Smith, P. W. (2013) Design, synthesis, and biological evaluation of indole-2-carboxamides: A promising class of antituberculosis agents. J. Med. Chem., 56 (21) 8849-8859.
2 Shattat, G., Al-Qirim, T., Abu Sheikha, G., Al-Hiari, Y., Sweidan, K., Al-Qirim, R., Hikmat, S., Hamadneh, L., and Al-Kouz, S. (2013) The Pharmacological effects of novel 5-fluoro-N-(9,10-dihydro-9,10-dioxoanthracen-8-yl)-1H-indole-2-carboxamide derivatives on plasma lipid profile of Triton-WR-1339-induced Wistar rats J. Enzyme Inhib. Med. Chem., 28 (4) 863-869.
3 Sweidan, K., Sabbah, D., Bardaweel, S., Abu Dush, K., Abu Sheikha, G., and Mubarak, M. S. (2016) Computer-aided design, synthesis, and biological evaluation of new indole-2-carboxamide derivatives as PI3Kα/EGFR inhibitors Bioorg. Med. Chem. Lett., 26 (11) 2685-2690.
4 Sweidan, K., Sabbah, D., Bardaweel, S., Abu Sheikha, G., Al-Qirim, T., and Salih, H. (2017) Facile synthesis, characterization, and cytotoxicity study of new 3-(indol-2-yl)bicyclotetrazatridecahexaens Can. J. Chem., 95 (8) 858-862.
5 Shivaraj, Y., Naveen, M. H., Vijayakumar, G. R., and Kumar, D. B. A. (2013) Design, synthesis and antibacterial activity studies of novel quinoline carboxamide derivatives J. Korean Chem. Soc., 57 (2) 241-245.
6 Lanigan, R. M., and Sheppard, T. D. (2013) Recent developments in amide synthesis: Direct amidation of carboxylic acids and transamidation reactions Eur. J. Org. Chem., 2013 (33) 7453-7465.
7 Mallah, E., Sweidan, K., Engelmann, J., Steimann, M., Kuhn, N., and Maier, M. E. (2012) Nucleophilic substitution approach towards 1,3-dimethylbarbituric acid derivatives—new synthetic routes and crystal structures Tetrahedron, 68 (4) 1005-1010.
8 Rao, D. V., Ramana, V. V. R., and Raghunanda, P. (1985) Studies on embelin. Part III. Synthesis and biological activity of some anthranilic acid ester derivatives of embelin and embelin di-O-methyl ether. Indian J. Chem. B, 24B (9) 988-991.
9 CrysalisPro Software System (version 1.171.35.11; release 16-05-2011), Intelligent Data Collection and Processing Software for Small Molecule and Protein Crystallography, Agilent Technologies Ltd., Yarnton, Oxfordshire (U.K.), (2011).
10 G. M. Sheldrick, Shelxtl (version 6.10), Bruker Analytical X-ray Instruments Inc., Madison, WI (USA), 2000.Sheldrick, GM., (SHELXL-97, Program for X-ray Crystal Structure Refinement) (Göttingen, Germany: University of Göttingen, 1997).
11 Images generated using Diamond (R): A crystal and molecular structures program for Windows. Crystal Impact GbR, Bonn, Germany, version 3.1a (2005). Author: Klaus Brandenburg.
2 Shattat, G., Al-Qirim, T., Abu Sheikha, G., Al-Hiari, Y., Sweidan, K., Al-Qirim, R., Hikmat, S., Hamadneh, L., and Al-Kouz, S. (2013) The Pharmacological effects of novel 5-fluoro-N-(9,10-dihydro-9,10-dioxoanthracen-8-yl)-1H-indole-2-carboxamide derivatives on plasma lipid profile of Triton-WR-1339-induced Wistar rats J. Enzyme Inhib. Med. Chem., 28 (4) 863-869.
3 Sweidan, K., Sabbah, D., Bardaweel, S., Abu Dush, K., Abu Sheikha, G., and Mubarak, M. S. (2016) Computer-aided design, synthesis, and biological evaluation of new indole-2-carboxamide derivatives as PI3Kα/EGFR inhibitors Bioorg. Med. Chem. Lett., 26 (11) 2685-2690.
4 Sweidan, K., Sabbah, D., Bardaweel, S., Abu Sheikha, G., Al-Qirim, T., and Salih, H. (2017) Facile synthesis, characterization, and cytotoxicity study of new 3-(indol-2-yl)bicyclotetrazatridecahexaens Can. J. Chem., 95 (8) 858-862.
5 Shivaraj, Y., Naveen, M. H., Vijayakumar, G. R., and Kumar, D. B. A. (2013) Design, synthesis and antibacterial activity studies of novel quinoline carboxamide derivatives J. Korean Chem. Soc., 57 (2) 241-245.
6 Lanigan, R. M., and Sheppard, T. D. (2013) Recent developments in amide synthesis: Direct amidation of carboxylic acids and transamidation reactions Eur. J. Org. Chem., 2013 (33) 7453-7465.
7 Mallah, E., Sweidan, K., Engelmann, J., Steimann, M., Kuhn, N., and Maier, M. E. (2012) Nucleophilic substitution approach towards 1,3-dimethylbarbituric acid derivatives—new synthetic routes and crystal structures Tetrahedron, 68 (4) 1005-1010.
8 Rao, D. V., Ramana, V. V. R., and Raghunanda, P. (1985) Studies on embelin. Part III. Synthesis and biological activity of some anthranilic acid ester derivatives of embelin and embelin di-O-methyl ether. Indian J. Chem. B, 24B (9) 988-991.
9 CrysalisPro Software System (version 1.171.35.11; release 16-05-2011), Intelligent Data Collection and Processing Software for Small Molecule and Protein Crystallography, Agilent Technologies Ltd., Yarnton, Oxfordshire (U.K.), (2011).
10 G. M. Sheldrick, Shelxtl (version 6.10), Bruker Analytical X-ray Instruments Inc., Madison, WI (USA), 2000.Sheldrick, GM., (SHELXL-97, Program for X-ray Crystal Structure Refinement) (Göttingen, Germany: University of Göttingen, 1997).
11 Images generated using Diamond (R): A crystal and molecular structures program for Windows. Crystal Impact GbR, Bonn, Germany, version 3.1a (2005). Author: Klaus Brandenburg.