Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/21699
Title: Synthesis of biologically active 3,8-dioxo-10-hydroxypyrano[2,3-f]quinoline and its reactions
Authors: Choudhari, B P
Mulwad, V V
Issue Date: Sep-2003
Publisher: NISCAIR-CSIR, India
Abstract: 6-Aminocoumarin 1 on heating with malonic acid and phosphorousoxychloride in the presence of naphthalene gives 3H-7,8-dihydro-3,8-dioxo-10-hydroxypyrano[2,3,f]quinoline 2. Compound 2 on further treatment with various acyclic, cyclic,aromatic, heterocyclic β-keto esters like ethyl acetoacetate, methyl salicylate, ethyl cyclopentanone-2-carboxylatc and ethyl 2,3-dihydro-3-oxobenzofuran-2-carhoxylate separately undergoes Peechman condensation to yield 3H, 11H-7,8-dihydro-9-methyl-3,8,11-trioxodipyrano[2,3-f; 2,3-c]quinoline 3, 3H-7,8,9, 10,11,12-hexahydro-3,8,12-trioxopyrano[2,3-f ]quinolino[3,4-b] pyrano[3,4-a] cyclopentane 4. 3H, 13H-7,8-dihydro-3,8, 13 trioxopyrano[2,3-f ]quinolino[3,4-b]-[1]-benzopyran 5. and 3H, 14H-7,8-dihydro-3,8, 14 trioxopyrano[2,3-f ]quinolino[3,4-b] -pyrano[3,4-b]-[1]-benzopyran 6 respectively. Also the reaction of isatin, malononitrile and the compound 2 affords the corresponding spiro-[3H-indol-(1H, 2 H)-3,9-((3H,7H,8H)-dipyrano[2,3-f; 2,3-c]quinoline]-11-amino-10-cyano-2,3,8-trione 7. The structures of all the compounds have been confirmed on the basis of spectral and analytical data. The above compounds have been screened for their antimicrobial activities and arc found to possess significant antibacterial and antifungal activities.
Page(s): 2080-2085
URI: http://hdl.handle.net/123456789/21699
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.42B(09) [September 2003]

Files in This Item:
File Description SizeFormat 
IJCB 42B(9) 2080-2085.pdf330.19 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.