Synthesis of biologically active thiazolo-benzopyranyl-s-triazine derivatives

Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry

Volumn 42, Issue 3, 2003, Pages 621-626

  Mulwad, V V ^a   Shirodkar, Jyoti M ^a  

^a INSTITUTE OF SCIENCE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

2 (2' AMINO 7' OXO 7'H [6']THIAZOLO[5',4' D] 4 (6'' THIOUREIDO 2''H [1''] 2'' OXOBENZOPYRANYL) 6 CHLORO S TRIAZINE; 2 (2' AMINO 7' OXO 7'H [6']THIAZOLO[5',4' D]BENZOPYRANYL) 4 (6'' THIOUREIDO 2''H [1''] 2'' OXOBENZOPYRANYL) 6 (6''' THIOUREIDO 2''' H [1'''] 2''' OXOBENZOPYRANYL) 6 CHLORO S TRIAZINE; 2 (2' AMINO 7' OXO 7'H [6]THIAZOLO[5,4' D]BENZOPYRANYL) 4,6 DICHLORO S TRIAZINE; 2 AMINO 7H [6]THIAZOLO[5,4 D]BENZOPYRAN 7 ONE; 6 AMINO 2 OXO 2H [1]BENZOPYRAN; 6 THIOUREIDO 2H [1]BENZOPYRAN 2 ONE; ACETIC ACID; ALCOHOL; BENZOPYRAN DERIVATIVE; BROMINE; CYANURIC ACID; HYDROCHLORIC ACID; THIAZOLOBENZOPYRANYL S TRIAZINE; THIOCYANATE; THIOCYANIC ACID DERIVATIVE; TRIAZINE DERIVATIVE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ARTICLE; CYCLIZATION; DRUG ACTIVITY; DRUG STRUCTURE; DRUG SYNTHESIS; GRAM NEGATIVE BACTERIUM; GRAM POSITIVE BACTERIUM; NONHUMAN; OXIDATION; SPECTROSCOPY;

EID: 0037366644     PISSN: 03764699     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (23)

1. Bansal R K, Heterocyclic chemistry, syntheses, reactions and mechanisms (Wiley Eastern Ltd. New Delhi), 1990, 242.
2. Nakazato, Atsuro, Skiguchi, Yoshinori, Kawashima, Yutaka, Chem Abstr, 199, 1993, 8801h.
3. El Mouafi H M R, Egypt J Pharm Sci, 32, 1991, 889.
4. Mohareb R M, Shams H Z & Elkholy Y M, Phosphorous, Sulphur, Silicon, Relat Elem, 1992, 317.
5. Kreutzberger A E, J Heterocyclic Chem, 19, 1982, 753.
6. Seale E E, Can Med Assoc J, 65, 1951, 582; Bhargava & Jose K, J Indian Chem Soc, 27, 1960, 314; Bhargava & Jose K, J Indian Chem Soc, 27, 1960, 314; Mackie & Mishra A L, J Chem Soc, 1954, 330.
7. Seale E E, Can Med Assoc J, 65, 1951, 582; Bhargava & Jose K, J Indian Chem Soc, 27, 1960, 314; Bhargava & Jose K, J Indian Chem Soc, 27, 1960, 314; Mackie & Mishra A L, J Chem Soc, 1954, 330.
8. Seale E E, Can Med Assoc J, 65, 1951, 582; Bhargava & Jose K, J Indian Chem Soc, 27, 1960, 314; Bhargava & Jose K, J Indian Chem Soc, 27, 1960, 314; Mackie & Mishra A L, J Chem Soc, 1954, 330.
9. Freidheim E A H, Schweiz Med Wochsch, 1941, 71, 116; Buckley S H & Crossley M L, Cancer Res, 10, 1950, 207.
10. Freidheim E A H, Schweiz Med Wochsch, 1941, 71, 116; Buckley S H & Crossley M L, Cancer Res, 10, 1950, 207.
11. Toyoma Chemical Industry Co. L. T. D., Chem Abstr, 64, 1966, 1131.
12. Yasuo M & Kivoshi S, Chem Abstr, 59, 1963, 5137; Jaques R, Helv Chim Acta, 33, 1950, 378.
13. Yasuo M & Kivoshi S, Chem Abstr, 59, 1963, 5137; Jaques R, Helv Chim Acta, 33, 1950, 378.
14. Bose P K, J Indian Chem Soc, 35, 1958, 367.
15. Sethna N K & Shah N M, Chem Rev, 36, 1945, 1.
16. Sangwan N K, Verma B S, Malik O P, & Dhindsa K S, Indian J Chem, 29 B, 1990, 294.
17. Stahman M A, Huebner C F, & Link K P, J Biol Chem, 138, 1941, 517.
18. Parrish J A, Fitzpatrick T B, Tanenbaum L, Patahak M A, New Engl, J Med, 291, 1974, 206.
19. Schuda P F, Top Org Chem, 91, 1980, 75.
20. Honmantgad S S, Kulkarni M V & Patil V D, Indian J Chem, 24B, 1985, 459.
21. Hapworth J D, Comprehensive, heterocyclic chemistry, Vol. 3, edited by J A Boulton and A Mikillap (Pergaman Press, Oxford) 1984, 737.
22. Mantulin W W & Sony P S, J Am Chem Soc, 95, 1973, 5122.
23. th Edn, Vol. II (C. V. Mosby company), 1970, 1406.