A simple and convenient synthesis of 4,6-disubstituted 3-cyanopyridin-2(1H)-ones under solvent-free microwave conditions

Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry

Volumn 43, Issue 4, 2004, Pages 885-887

  Dave, Chaitanya G ^a,b   Shah, Dhaval A ^a,c   Agrawal, Yadvendra K ^a  

^a GUJARAT UNIVERSITY   (India)

^b ZYDUS RESEARCH CENTRE   (India)

^c M G SCIENCE INSTITUTE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

3 CYANOPYRIDIN 2(1H) ONE DERIVATIVE; ACETAMIDE DERIVATIVE; CHALCONE; NITRILE; POTASSIUM HYDROXIDE; PYRIDONE DERIVATIVE; SOLVENT; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; INTERMETHOD COMPARISON; MICROWAVE IRRADIATION; SYNTHESIS;

EID: 2342535129     PISSN: 03764699     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (38)

1. (a) Lee L F & Normansell J E, J Org Chem, 55, 1990, 2964.
2. (b) Murry T J & Zimmerman S C, Tetrahedron Lett, 36, 1995, 7627.
3. (a) Schultz A G, Chem Rev, 73, 1973, 385.
4. (b) Jones G, Pyridines and their Benzo Derivatives: (V) Reactivity of Non-aromatics, Comprehensive Heterocyclic Chemistry, Vol. 2, edited by Katrizky A R & Rees C W, (Pergamon Press, Oxford), 1984, 395.
5. (c) Beak P, Covington J B, Smith S G, White J & Zeigler J M, J Org Chem, 45, 1980, 1354.
6. (d) Youngdale G A & Oglia T F, J Med Chem, 28,1985, 1790.
7. (a) Bharat C, J Indian Chem Soc, 7, 1930, 321.
8. (b) Basu U, J Indian Chem Soc, 7, 1930, 481.
9. (c) Basu U, J Indian Chem Soc, 7, 1930, 815.
10. (d) Bharat C, J Indian Chem Soc, 7, 1930, 851.
11. (e) Basu U, J Indian Chem Soc, 8, 1931, 119.
12. Reid W & Meyer A, Chem ber, 90, 1957, 2841.
13. Sakurai A & Midorikawa H, Bull Chem Soc Jpn, 40(7), 1967, 1680.
14. (a) Bomika Z, Andaburskaya M B, Pelcers J & Duburs G, Khim Geterotsikl Soedin, 8, 1975, 1108.
15. (b) Al-Hajjar F H & Jarrar A A, J Heterocycl Chem, 17(7), 1980, 1521.
16. (a) Moussa H H & Chabaka L M, Egypt J Chem, 26(3), 1983, 267.
17. (b) Jain R, Roschangar F & Ciufolini M A, Tetrahedron Lett, 36(19), 1995, 3307.
18. Soto J L, Seoane C & Mansilla A M, Org Prep Proced Int, 13(5), 1981, 331.
19. Kambe S, Saito K, Sakurai A & Hayashi T, Synthesis, 1977, 841.
20. (a) Isao S, Bull Chem Soc Jpn, 52(4), 1979, 1235.
21. (b) Isao S, Tokyo Kogyo Shikensho Hokoku, 76(9), 1981, 635.
22. Alberola A, Andres C, Gonzalez O A, Pedrosa R & Vincente M, J Heterocycl Chem, 24(3), 1987, 709.
23. (a) Abramovich R A, Org Prep Proceed Int, 23, 1991, 683.
24. (b) Laurent R, Laporterie A, Berlan J D J, Lefeuvre S & Audhuy M, J Org Chem, 57, 1992, 7099.
25. (c) Bose A, Manhas M, Shah M, Raju V, Bari S, Newz S, Banik B, Chaudary A & Barakat K, J Org Chem, 58, 1991, 6968.
26. (d) Caddick S, Tetrahedron, 51, 1995, 10403.
27. (a) Varma R S, Dahiya R & Saini R K, Tetrahedron Lett, 38, 1997, 8819.
28. (b) Varma R S, Dahiya R & Saini R K, Tetrahedron Lett, 38, 1997, 7029.
29. Dave C G & Shah R D, Heterocycles, 51(8), 1999, 1819.
30. Dave C G & Cicily A, Indian J Chem, 39B, 2001, 403.
31. Dave C G & Joshipura H M, Indian J Chem, 41B, 2002, 650.
32. Sharp J T, Gosney I & Rowley A G, Practical Organic Chemistry (Chapman & Hall,: London) 1990, 65
33. Chincholkar M M, Kakade B S & Jamode V S, Acta Cienc Indica, 9, 1983, 47.
34. Sammour A, Selim M I B & AbdElhalim M S, Egypt J Chem, 15, 1972, 23.
35. Sammour A, Akhnookh Y & Jahine H, UAR J Chem, 13, 1970, 421.
36. Sammour A, Fahmy A F, Abd El-Rahman S, Akhnookh Y & Abd Elmoez M S, UAR J Chem, 13, 1970, 421.
37. Kuthan J, Nesvadba P, Popl M & Fahnrich J, Collect Czech Chem Comnmn, 44(8), 1979, 2409.
38. Abdalla M, Essawy A & Deeb A, Pak J Sci Ind Res, 20(3), 1977, 139.