Author(s):
Anil B. Chidrawar, Rajkumar U. Pokalwar, Nitishkumar S. Kaminwar
Email(s):
anilchidrawar74@gmail.com
DOI:
10.5958/0974-360X.2020.00472.2
Address:
Anil B. Chidrawar1*, Rajkumar U. Pokalwar1, Nitishkumar S. Kaminwar2
1P G Research Centre, Department of Chemistry, Degloor College, Degloor, S.R.T.M.U. Nanded, India – 431717.
2P G Department of Chemistry, L. B. S. College, Dharmabad, S.R.T.M.U. Nanded, India - 431717.
*Corresponding Author
Published In:
Volume - 13,
Issue - 6,
Year - 2020
ABSTRACT:
A mixture of Bis methylthio methylene malononitrile (BMMM), thiourea and aniline/4-chloro aniline/4-methoxy aniline/4-nitro aniline on reflux with dimethyl formamide solvent in presence of K2CO3 for 5-6 hours. The progress of the reaction was monitored by TLC. After completion of the reaction, the mixture was cooled to room temperature, washed with water gives 2,6-dihydro-2,6-diimino-4,8-bis (phenylamino) pyrimido [2,1-b] [1,3] thiazine-3,7-dicarbonitrile and its derivatives respectively. The synthesized compounds were characterized by elemental analysis and spectral data.
Cite this article:
Anil B. Chidrawar, Rajkumar U. Pokalwar, Nitishkumar S. Kaminwar. An effective multicomponent synthesis of 2,6-dihydro-2,6-diimino-4,8-bis (phenylamino) pyrimido [2,1-b] [1,3] thiazine-3,7-dicarbonitrile. Research J. Pharm. and Tech 2020; 13(6):2658-2660. doi: 10.5958/0974-360X.2020.00472.2
Cite(Electronic):
Anil B. Chidrawar, Rajkumar U. Pokalwar, Nitishkumar S. Kaminwar. An effective multicomponent synthesis of 2,6-dihydro-2,6-diimino-4,8-bis (phenylamino) pyrimido [2,1-b] [1,3] thiazine-3,7-dicarbonitrile. Research J. Pharm. and Tech 2020; 13(6):2658-2660. doi: 10.5958/0974-360X.2020.00472.2 Available on: https://rjptonline.org/AbstractView.aspx?PID=2020-13-6-22
REFERENCES :
1. Deepika G., Gopinath P., Kranthi, G., Nagamani C., Jayasree Y.V., Naidu N.V., Enaganti S., J. Pharm. Res., 2012; 5: 1105–1107.
2. Chaviara A.T., Cox P.J., Repana K.H., Papi R.M., Papazisis K.T., Zambouli D., Kortsaris A.H., Kyriakidis D.A., Bolos C.A., J. Inorg. Biochem., 2004; 98: 1271–1283.
3. D.B. Reddy, S. Reddy, N.S. Reddy and M.V.R. Reddy, Indian J. Chem., Sect. B., 1991; 30: 529–533.
4. M.E. Arranz, J.A. Diaz, S.T. Ingate, M. Witvrouw, C. Pannecouque, J. Balzarini, E. De Clercq and S. Vega, Bioorg. Med. Chem., 1999; 7: 2811–2822.
5. H. Moriyama, T. Tsukida, Y. Inoue, K. Yokota, K. Yoshino, H. Kondo, N. Miura and S. Nishimura, J. Med. Chem., 2004; 47: 1930–1938.
6. D. Armenise, G. Trapani, V. Arrivo and F. Morlacchi, Arch. Pharm., 1998; 331: 54–58.
7. G. Trippe, J. Perron, A.J. Marchand, V. Dupont, A. Guingant, J.P. Pradere and L. Toupet, Tetrahedron Lett., 2002; 43: 6067–6069.
8. M. Koketsu, K. Tanaka, Y. Takenaka, C.D. Kwong and H. Ishihara, Eur. J. Pharm. Sci., 2002; 15: 307–310.
9. M. Harmata, X. Hong and C.L. Barnes, Tetrahedron Lett., 2003; 44: 7261–7264.
10. T. Noshio, Y. Konno, M. Ori and M. Sakamoto, Eur. J. Org. Chem., 2001; 3533–3537.
11. L.D.S. Yadav and A. Singh, Tetrahedron Lett., 2003; 44: 5637–5640.
12. L.D.S. Yadav and S. Sharma, Synthesis, 1992; 919–920.
13. P. Pajesi, A. Foldesi, G. Batta and J. Tamas, Chem. Ber., 1989; 122: 651–653.
14. R. Okazaki, M. Unno and N. Inamoto,Heterocycles, 1987; 25: 183–190.
15. W. Hanfeld, Arch. Pharm., 1984; 317: 297–299.
16. K. Burger, E. Huber, W. Schontag and R. Ottlinger, J. Chem. Soc., Chem. Commun., 1983; 944–945.
17. (a) K. Kiec-Kononowicz, J. Karolak-Wojciechowska, C.E. Muller, B. Schumacher, E. Pekala and E. Szymanska, Eur. J. Med. Chem., 2001; 36: 407–419; (b) U. Geis, K. Kiec-Kononowicz and C.E. Muller, Sci. Pharm., 1996; 64: 383–390.
18. D. Bozsing, P. Sohar, G. Gigler and G. Kovacs, Eur. J. Med. Chem., 1996; 31: 663–668.