Synthesis, crystal structure and DFT study of N-(6-sulfamoylpyridin-3-yl)acetamide

References

• K. Radha, J. Kyu-Yeon, M. K. Tara, S. Somin, B. T. M. Til, B. Ganesh, S. Aarajana, N. Younghwa, K. Youngjoo, K. Eung-Seok, Eur. J. Med. Chem. 113, 228–245 (2016). DOI: 10.1016/j.ejmech.2016.02.050
   PubMed Web of Science ®Google Scholar
• N. Kazutaka, T. Itaru, T. Keigo, M. Masayuki, H. Toru, I. Satoshi, M. Norio, A. Shinya, U. Norihiro, M. Mamiko, W. Naoaki, A. Makoto, Y. Kentaro, H. Katsura, Bioorg. Med. Chem. Lett. 20, 4624–4626 (2010). DOI: 10.1016/j.bmcl.2010.06.005
   PubMed Web of Science ®Google Scholar
• A. B. Etify, A. A. Aly, E. A. E. Mohamed, A. A. A. Shaban, J. Agric. Food Chem. 62, 9982–9886 (2014). DOI: 10.1021/jf503992y
   PubMed Web of Science ®Google Scholar
• N. Mina, K. TaeHun, K. Jinsook, H. S. Seon, K. K. Min, K. K. Eun, M. Sun-Joon, S. C. Yong, K. Gyochang, B. Du-Jong, L. Jiyoun, N. P. Ae, Eur. J. Med. Chem. 97, 245–258 (2015). DOI: 10.1016/j.ejmech.2015.04.060
   PubMed Web of Science ®Google Scholar
• S. Feng, W. Luling, H. Xian, J. Org. Chem. 77, 3754–3765 (2012). DOI: 10.1021/jo300072x
   PubMed Web of Science ®Google Scholar
• S. Feng, H. Xian, Ange. Chem. 48, 3458–3461 (2009). DOI: 10.1002/ange.200900212
   Google Scholar
• P. L George, C. Daniel, D. B. James, Bioorg. Med. Chem. 17, 4127–4133 (2009). DOI: 10.1016/j.bmc.2009.01.018
   PubMed Web of Science ®Google Scholar
• S. Hisahiro, K. Junji, Chem. Mater. 23, 621–630 (2011). DOI: 10.1021/cm1024052
   Web of Science ®Google Scholar
• N. F. Lazareva, Russ. Chem. Bull. 60, 615–632 (2011). DOI: 10.1007/s11172-011-0097-8
   Web of Science ®Google Scholar
• S. Mahesh, K. C. Tang, M. Raj, Molecules. 23, 2615–2658 (2018). DOI: 10.3390/molecules23102615
   PubMed Web of Science ®Google Scholar
• A. Ivana, p. Milos, J. Milos, M. Dusan, V. Branka, N. Jasmina, S. A. Lidija, Front. Microbiol. 8, 2454–2470 (2018). DOI: 10.3389/fmicb.2017.02454
   Google Scholar
• I. O. Zhuravel, S. M. Kovalenko, A. V. Ivachtchenko, K. V. Balakin, V. V. Kazmirchuk, Bioorg. Med. Chem. Lett. 15, 5483–5487 (2005). DOI: 10.1016/j.bmcl.2005.08.081
   PubMed Web of Science ®Google Scholar
• E. P. McMoran, M. N. Dominguez, E. M. Erwin, D. R. Powell, G.T. Rowe, L. Yang, Inorganica Chimica Acta. 46, 150–160 (2016). DOI: 10.1016/j.ica.2016.03.011
   Google Scholar
• R. Alam, M. A. Alam, A. K. Panda, Rahisuddin, Med. Chem. Res. 27, 560–570 (2018). DOI: 10.1007/s00044-017-2082-8
   Web of Science ®Google Scholar
• T. X. Li, J. Zhang, J. Pan, Z. X. Wu, D. Hu, B. Song, Eur. J. Med. Chem., 125, 657–662 (2017). DOI: 10.1016/j.ejmech.2016.09.069
   PubMed Web of Science ®Google Scholar
• J. J. Li, M. B. Norton, E. J. Reinhard, G. D. Anderson, S. A. Gregory, P. C. Isakson, C. M. Koboldt, J. L. Masferrer, W. E. Perkins, K. Seibert, Y. Zhang, B. S. Zweifel, D. B. Reitz, J. Med. Chem. 39, 1846–1856 (1996). DOI: 10.1021/jm950878e
   PubMed Web of Science ®Google Scholar
• A. Natarajan, Y. H. Guo, F. Harbinski, Y. Fan, L. Luus, J. Diercks, H. Aktas, M. Chorev, J. A. Halperin, J. Med. Chem. 47, 4979–4982 (2004). DOI: 10.1021/jm0496234
   PubMed Web of Science ®Google Scholar
• C. Chen, Y. Luo, H. Yin, Q. Zhong, S. Zheng, C. Zhao, G. Wang, L. He, Bioorg. Med. Chem. 60, 116626 (2022). DOI: 10.1016/j.bmc.2022.116626
   PubMedGoogle Scholar
• A. K. Ganguly, S. S. Alluri, D. Caroccia, J. Med. Chem. 54, 7176–7183 (2011). DOI: 10.1021/jm200778q
   PubMed Web of Science ®Google Scholar
• Z. M. Zhong, R. Chen, R. G. Xing, X. L. Chen, S. Liu, Z. Y. Guo, X. Ji, L. Wang, P. C. Li, Carbohydr. Res. 342, 2390–2395 (2007). DOI: 10.1016/j.carres.2007.07.015
   PubMed Web of Science ®Google Scholar
• T. W. Jabusch, R. S. Tjeerdema, J. Agric. Food Chem. 53, 7179–7183 (2005). DOI: 10.1021/jf050767g
   PubMed Web of Science ®Google Scholar
• Y. Liu, Y. L. Zhao, Q. Ren, Z. X. Zhou, H. F. Chai, C. S. Zhao, J. Mol. Struct. 1208, 127869 (2020). DOI: 10.1016/j.molstruc.2020.127869
   Google Scholar
• N. Muhammad, M. Ahmad, M. Sirajuddin, Z. Ali, N. Tumanov, J. Wouters, A. Chafik, K. Solak, A. Mavi, Z. Ali, S. Muhammad, S. Shujah, S. Ali, A. G. Al-Sehemi, Front. Pharmacol. 13, 864336 (2022). DOI: 10.3389/fphar.2022.864336
   PubMedGoogle Scholar
• Q. Ren, H. P. Huang, W. K. Liao, Z. X. Zhou, C. S. Zhao, J. Struct. Chem. 62, 1472–1482 (2021). DOI: 10.1134/s0022476621090171
   Web of Science ®Google Scholar
• M. Dinçer, D. Avci, M.Sekerci, Y. Atalay, J. Mol. Model. 14, 823–832 (2008). DOI: 10.1007/s00894-008-0324-x
   PubMed Web of Science ®Google Scholar
• B.J. Deppmeier, A.J. Driessen, The Chemist’s Companion. Wavefunction. Spartan ‘08 (Irvine: Wavefunction.Inc, 2009).
   Google Scholar
• S. Chamberland, J.W. Ziller, K.A. Woerpel, J.Am.Chem.Soc. 127, 5322–5323 (2005). DOI: 10.1021/ja050830i
   PubMed Web of Science ®Google Scholar
• P. Politzer, J.S. Driessen, The Chemist’s Companion. In Theoretical Biochemistry and Molecular Biophysics: A Comprehensive Survey (New York: Schenectady Adenine Press, 1990), p. 45.
   Google Scholar
• F. Benhiba, N. K. Sebbar, H. Bourazmi, M. E. Belghiti, R. Hsissou, T. Hokelek, A. Bellaouchou, A. Guenbour, I. Warad, H. Oudda, A. Zarrouk, E.M. Essassi, Int. J. Hydrogen Energy. 46, 25800–25818 (2021). DOI: 10.1016/j.ijhydene.2021.05.091
   Web of Science ®Google Scholar
• J. F. Lu, P. Huang, D. Zhang, Q. Wang, N. Zheng, R. Wu, Q. Liu, L. X. Jin, X. H. Jin, X. H. Ji, Y. H. Gao, H. G. Ge, J. Mol. Struct. 1210, 127996 (2020). DOI: 10.1016/j.molstruc.2020.127996
   Web of Science ®Google Scholar
• F. Javed, M. Sirajuddin, S. Ali, N. Khalid, M. N. Tahir, N. A. Shah, Z. Rasheed, M. R. Khan, Polyhedron 104, 80–90 (2016). DOI: 10.1016/j.poly.2015.11.041
   Web of Science ®Google Scholar
• M. Tariq, R. Khan, A. Hussain, A. Batool, F. Rasool, M. Yar, K. Ayub, M. Sirajuddin, F. Ullah, S. Ali, A. Akhtar, S. Kausar, A. A. Altaf, J. Coord. Chem. 74, 2407–2426 (2021). DOI: 10.1080/00958972.2021.1964019
   Web of Science ®Google Scholar
• R. Zafar, M. Zubair, S. Ali, K. Shahid, W. Waseem, H. Naureen, A. Haider, M. S. Jan, F. Ullah, M. Sirajuddin, A. Sadiq, J. Biomol. Struct. Dyn. 39, 1044–1054(2021). DOI: 10.1080/07391102.2020.1724569
   PubMed Web of Science ®Google Scholar
• E. Pretsch, P. Buhlmann, The Chemist’s Companion. Structure Determination of Organic Compounds Tables of Spectral Data (Germany: springer, 2009).
   Google Scholar
• N. Kanagathara, A. F. Mary, V. Ragavendran, D. Dhanasekaran, R. Usha, R.G.S. Rao, J. Mol. Struct. 1223, 128965 (2021). DOI: 10.1016/j.molstruc.2020.128965
   Google Scholar
• Khan, S. A., Khan, E., Noor, A., Schwarz, S., J. Struct. Struct. 16, 159–167 (2019). DOI: 10.1134/s0022476619010220
   Google Scholar