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We have demonstrated two step one-pot synthesis of novel 5-(4-Fluorophenyl)-1H-Beno[e][1,4]Diazepin-2(3H)-one using 2-Amino-4’-fluorobenzophenone as initial stating material. The small library of N-alkylation and C-3 benzylidene derivatives have been synthesized by base catalyzedreaction of 5-(4-fluorophenyl)-1H-benzo[e][1,4]diazepin-2(3H)-one (3) nucleus with various alkyl halides and aromatic aldehydes respectively.
Słowa kluczowe
Rocznik
Tom
Strony
106--115
Opis fizyczny
Bibliogr. 18 poz., tab., wz.
Twórcy
autor
- Department of Chemistry, Saurashtra University, Rajkot, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot, Gujarat, India
Bibliografia
- [1] K. Rohtash, J. Lown, Mini-Reviews in Medicinal Chemistry 3 (2003) 323.
- [2] L. Bertelli, et al., J. Pharmacy and Pharmacology 54 (2002) 827.
- [3] I. Braulio, O. Fabian, L. Carolina, Q. Jairo, A. Rodrigo, H. Mike, N. Manuel, C. Justo, Bioorganic & Medicinal Chemistry 16 (2008) 8492.
- [4] R. Haris, J. Straley, US patent 1, 537, 757, (1968).
- [5] A. Kondaskar, et al., Med. Chem. Lett. 2 (2011) 252.
- [6] M. Di Braccio, G. Grossi, G. Romoa, L. Vargiu, M. Mura, M. Marongiu, Eur. J. Med. Chem. 36 (2001) 935.
- [7] A. El-Sayed, A. Khodairy, H. Salah, H. Abdel-Ghany, Phosphorus Sulfur Silicon Relat. Elem. 182 (2007) 711.
- [8] R. Claramunt, D. Sanz, S. Aggarwal, A. Kumar, O. Prakash, S. Singh, J. Elgueroc, Arkivoc. 14 (2006) 35.
- [9] M. Balakrishna, B. Kaboudin, Tetrahedron Lett. 42 (2001) 1127.
- [10] B. Kaboudin, K. Navaee, Heterocycles 55 (2001) 1443.
- [11] M. Pozarentzi, et al., Tetrahedron Lett. 44 (2003) 1835.
- [12] J. Yadav, B. Reddy, S. Kumar, K. Nagaiah, Synthesis. (2005) 480.
- [13] S. De, R. Gibbs, Tetrahedron Lett. 46 (2005) 1811.
- [14] B. Reddy, P. Sreekanth, P. Lakshmanan, J. Mol. Catal. A: Chem. 237 (2005) 93.
- [15] J. Yadav, B. Reddy, G. Satheesh, G. Srinivasulu, A. Kunwar, Arkivoc 3 (2005) 221.
- [16] R. Varala, E. Ramu, N. Sreelatha, S. Adapa, Synlett. (2006) 1009.
- [17] A. Katrizky, R. Abonia, B. Yang, M. Qi, B. Insuasty, Synthesis. (1998) 1487.
- [18] Jay Bhogayta, Taslimahemad Khatri, Vijay Ram, Pragnesh Dave, International Letters of Chemistry, Physics and Astronomy 10 (2014) 1-13.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-d8c09d42-1dab-4194-8902-116117a14edf