Microwave induced new route to acridine and quinazoline derivatives using TLC plates

Journal of Heterocyclic Chemistry

Volumn 42, Issue 4, 2005, Pages 703-705

  Kidwai, M ^a   Saxena, S ^a   Mohan, R ^a  

^a UNIVERSITY OF DELHI   (India)

Author keywords

[No Author keywords available]

Indexed keywords

3,3,6,6 TETRAMETHYL 9 (2 CHLORO 3 QUINOYL) 1,2,3,4,5,6,7,8,9,10 DECAHYDROACRIDINE 1,8 DIONE; 3,3,6,6 TETRAMETHYL 9 (4 CHLOROPHENYL) 1,2,3,4,5,6,7,8,9,10 DECAHYDROACRIDINE 1,8 DIONE; 3,3,6,6 TETRAMETHYL 9 PHENYL 1,2,3,4,5,6,7,8,9,10 DECAHYDROACRIDINE 1,8 DIONE; 3,3,6,6 TETRAMETHYL 9 PIPERONYL 1,2,3,4,5,6,7,8,9,10 DECAHYDROACRIDINE 1,8 DIONE; 4 (2 CHLORO 3 QUINOLYL) 7,7 DIMETHYL 5 OXO 1,2,3,4,5,6,7,8 OCTAHYDROQUINAZOLINE 2 THIONE; 4 (4 CHLOROPHENYL) 7,7 DIMETHYL 5 OXO 1,2,3,4,5,6,7,8 OCTAHYDROQUINAZOLINE 2 THIONE; 4 PHENYL 7,7 DIMETHYL 5 OXO 1,2,3,4,5,6,7,8 OCTAHYDROQUINAZOLINE 2 THIONE; 4 PIPERONYL 7,7 DIMETHYL 5 OXO 1,2,3,4,5,6,7,8 OCTAHYDROQUINAZOLINE 2 THIONE; ACRIDINE DERIVATIVE; QUINAZOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; METHODOLOGY; MICROWAVE IRRADIATION; PARALLEL DESIGN; SYNTHESIS; THIN LAYER CHROMATOGRAPHY;

EID: 19644381500     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570420435     Document Type: Article

References (17)

1. M. Kidwai, Pure Appl. Chem., 73, 1261 (2001).
2. [a] M. Kidwai, S. Saxena, R. Mohan and R. Venkataramanan, J. Chem. Soc.; Perkin Trans. 1, 16, 1845 (2002);
3. [b] M. Kidwai, R. Venkataramanan and B. Dave, J. Heterocyclic Chem., 39, 1045 (2002).
4. [a] A. Hantzsch, Justus Liebigs Ann. Chem., 1, 215 (1882);
5. [b] R. Alajarin, J. J. Vaquero, J. L. G. Navio and J. Alvarez-Builla, Synlett., 297 (1992).
6. [a] P. Biginelli, Gazz. Chim. Ital., 23, 360 (1893);
7. [b] C. O. Kappe, Tetrahedron, 49,6937 (1993);
8. [c] D. S. Bose, L. Fatima and H. B. Mereyala, J. Org. Chem., 68, 587 (2003).
9. [a] J. P. McCarthy, R. Zhang and S. Moreland, J. Med. Chem., 38, 119 (1995);
10. [b] R. Fossheim, K. Svarteng, A. Mostad, C. Romming, E. Shefter and D. J. Triggle, J. Med. Chem., 25, 126 (1982).
11. M. Kidwai and R. Mohan, Canadian J. Chem., 82, 427 (2004).
12. M. Kidwai, R. Mohan and S. Saxena, Russ. Chem. Bull., 52, 2457 (2003).
13. L. Williams, Chem. Commun., 435 (2000).
14. O. Meth Cohn, B. Narine and B. Tarnowski, J. Chem. Soc. Perkin Trans. 1, 1520 (1981).
15. N. Martin, M. Quinteiro and C. Sewane, J. Heterocyclic Chem., 32, 235 (1995).
16. S. J. Tu, Z. Lu, D. Shi, C. Yao, Y. Gao and C. Guo, Synth. Commun., 32(14), 2181 (2002).
17. M. Yarim, S. Sarac, M. Ertan, F. S. Kihc and K. Erol, Arzneimittel-Forschung, 52(1), 27 (2002).