A one-pot synthesis and self-assembled superstructure of organic salts of a 1,5-benzodiazepine derivative

Tetrahedron Letters

Volumn 47, Issue 18, 2006, Pages 3135-3138

  Thakuria, Harjyoti ^a   Pramanik, Avijit ^a   Borah, Ballav Moni ^a   Das, Gopal ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY GUWAHATI   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ACETONE; ACID; AMINE; BENZODIAZEPINE DERIVATIVE; CARBOXYLIC ACID; PICRIC ACID; SODIUM CHLORIDE; SOLVENT;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CRYSTAL; DRUG STRUCTURE; DRUG SYNTHESIS; HYDROGEN BOND; ROOM TEMPERATURE; STRUCTURE ANALYSIS; SUPRAMOLECULAR CHEMISTRY;

EID: 33645885349     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.02.137     Document Type: Article

References (29)

1. Krapcho J., and Turk C.F. J. Med. Chem. 9 (1966) 191-195
2. Sternback L.H. Angew. Chem., Int. Ed. Engl. 10 (1971) 34-43
3. Randall L.O., and Kappel B. In: Garattini S., Mussini E., and Randall L.O. (Eds). Benzodiazepines (1973), Raven Press, New York 27-51
4. Schutz H. Benzodiazepines (1982), Springer, Heidelberg
5. Essaber M., Baouid A., Hasnaoui A., Benharref A., and Lavergne J.P. Synth. Commun. 28 (1998) 4097-4104
6. El-Sayed A.M., Abdel-Ghany H., and El-Saghier A.M.M. Synth. Commun. 29 (1999) 3561-3572
7. Gringauz A. Introduction to Medicinal Chemistry (1999), Wiley-VCH
8. Morales H.R., Bulbarela A., and Conttreas R.R. Heterocycles 24 (1986) 135-139
9. Curini M., Epifano F., Marcotullio M.C., and Rosati O. Tetrahedron Lett. 42 (2001) 3193-3195
10. Balakrishna M.S., and Kaboudin B. Tetrahedron Lett. 42 (2001) 1127-1129
11. Zhong W., Zhang Y., and Chen X. Tetrahedron Lett. 42 (2001) 73-75
12. Reddy B.M., and Sreekanth P.M. Tetrahedron Lett. 44 (2003) 4447-4449
13. Yadav J.S., Reddy B.V.S., Eshwaraiah B., and Anuradha K. Green Chem. 4 (2002) 592-594
14. Jarikote D.V., Siddiqui S., Rajagopal R., Daniel T., Lahoti R.J., and Srinivasan K.V. Tetrahedron Lett. 44 (2003) 1835-1838
15. Voet D., and Voet J.G. Biochemistry (1995), Wiley, New York
16. Hanessian S., Simard M., and Roelens S. J. Am. Chem. Soc. 117 (1995) 7630-7645
17. Russel V.A., Etter M.C., and Ward M.D. J. Am. Chem. Soc. 116 (1994) 1941-1952
18. Lehn J.-M. Angew. Chem., Int. Ed. Engl. 29 (1990) 1304-1319
19. Desiraju G.R. Crystal Engineering: The Design of Organic Solids (1989), Elsevier, Amsterdam
20. Lange R.F.M., Beijer F.H., Sijbesma R.P., Hooft R.W.W., Kooijman H., Spek A.L., Kroon J., and Meijer E.W. Angew. Chem., Int. Ed. 36 (1997) 969-971
21. Ashton P.R., Brown C.L., Menzer S., Nepogodiev S.A., Stoddart J.F., and Williams D.J. Chem. Eur. J. 2 (1996) 580-591
22. Eichhorst-Gerner K., Stabel A., Moessner G., Declerq D., Valiyveettil S., Enkelmann V., Mullen K., and Rabe J.P. Angew. Chem., Int. Ed. 35 (1996) 1492-1495
23. Lehn J.-M. Supramolecular Chemistry: Concepts and Perspectives (1995), VCH, Weinheim
24. Whitesides G.M., Simanek E.E., Mathias J.P., Seto C.T., Chin D.N., Mammen M., and Gordon D.M. Acc. Chem. Res. 28 (1995) 37-44
25. Lawrence D.S., Jiang T., and Levett M. Chem. Rev. 95 (1995) 2229-2260
26. Berge S.M., Bighley L.D., and Monkhouse D.C. J. Pharm. Sci. 66 (1977) 1-19
27. -1 3290 (NH), 1638 (C{double bond, long}N), 1597 (Ar).
28. -1, Mo-Kα radiation, R1 = 0.0981, wR2 = 0.2826, S = 2.009. The crystallographic data for the complexes has been deposited with the Cambridge Crystallographic Data Centre. Copies of this information may be obtained free of charge from the Director, CCDC, 12 Union Road, Cambridge, CB2 1EZ, UK (Fax: +44 1223 336033; e-mail: deposit@ccdc.cam.ac.uk or http://www.ccdc.cam.ac.uk).
29. Naskar J.P., Hati S., Datta D., Samanta U., and Chakrabarti P. Z. Kristallogr. 213 (1998) 112-114