2003
DOI: 10.1002/chin.200322143
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Synthesis and Reactions of Pyranoquinolines.

Abstract: Fused pyridine derivativesFused pyridine derivatives R 0450 Synthesis and Reactions of Pyranoquinolines. -A facile synthesis of pyranoquinolines (V) from 6-aminocoumarins (I) and their use as building block for the synthesis of various new bridgehead N-heterocycles is described. -(MULWAD*, V. V.; DALVI, M. B.; Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 42 (2003) 2, 358-362; Dep. Chem., Inst. Sci., Bombay 400 032, India; Eng.) -M. Kowall 22-143

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Cited by 3 publications
(6 citation statements)
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“…. Let the mixture at room temperature then diluted with water and left overnight, precipitate was formed washed with 20 mL of a mixture of water/ethanol (1:1 v/v) then recrystallized from benzene to give compound (9).The melting point was (194-196°C). The physical properties are listed in Table 1.…”
Section: -Amino-4-(2-chloroquinolin-3-yl)-6-(4-hydroxyphenyl)-34-dimentioning
confidence: 99%
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“…. Let the mixture at room temperature then diluted with water and left overnight, precipitate was formed washed with 20 mL of a mixture of water/ethanol (1:1 v/v) then recrystallized from benzene to give compound (9).The melting point was (194-196°C). The physical properties are listed in Table 1.…”
Section: -Amino-4-(2-chloroquinolin-3-yl)-6-(4-hydroxyphenyl)-34-dimentioning
confidence: 99%
“…New absorption appeared at 1155 cm -1 for C=S group in pyrimidine ring, a medium absorption at 1558 cm -1 and at cm -1 for C=N and C=C corresponding to aromatic system. The IR spectral data for compound (9) showed the disappearance of absorption at 1673 cm -1 and 1601 cm -1 corresponding to C=O group and for olefinic double bond, and exhibited absorption at 3487 cm -1 for N-H group. The reaction of chalcone (4a) with hydrazine hydrate and phenyl hydrazine can formed pyrazoline (10,11).…”
Section: Scheme 5: the Mechanism Of Oxime Formationmentioning
confidence: 99%
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“…Chemistry of Quinoline derivatives has been of increasing Quinoline family compounds are widely used as a parent compound to make drugs, fungicides, biocides, alkaloids, dyes, rubber, chemicals, flavoring agents, antiseptic. [1] Quinoline derivatives have been reported anti-inflammatory [2] , antibacterial [3,4,5] , antifungal [6,7] , antiallergy [8] , antidepressant [9] , antiasthmatic [10] , antimalarial [11][12][13] , antiviral [14,15] , antitumour [16] , neuroleptic activity [17] , antihypertensive [18,19] , cytotoxic [20][21][22] , antihistamine [23] , CVS [24] , antiseptic, analgesic, antihelmintic [25] , hypnotic, sedative and CNS [26] , Bronchodilator activities [27] The present work we have attempted to combine the 3-formyl-6-nitroquinoline-2-thione with various aryl amines to get some novel 3-formyl-6-nitroquinoline-2-thionederivatives and screened for their possible anti-oxidant and wound healing properties.…”
Section: Introductionmentioning
confidence: 99%
“…Το αωζψθμα από τισ ρίηεσ του είδουσ αυτοφ χρθςιμοποιείται τόςο ςτθ κεραπεία τθσ ελονοςίασ, όςο και άλλων αςκενειϊν. Επίςθσ, δυο ακόμα χαρακτθριςτικά παραδείγματα ωυςικϊν κινολινικϊν παραγϊγων με βιολογικζσ δράςεισ είναι θ δυνεμικίνθ Α (60) και θ ςτρεπτονιγρίνθ (61), μζλθ μιασ ευρείασ ομάδασ αντικαρκινικϊν ωαρμάκων (Σχιμα 40).…”
Section: σχιμα 39unclassified