Synthesis of some Novel Pyrazolo and Triazolo Quinolines from Coumarin Compounds
Author(s) -
Shymaa S. Shawkat,
Adnan O. Omar
Publication year - 2012
Publication title -
mağallaẗ ʻulūm al-rāfidayn
Language(s) - English
Resource type - Journals
eISSN - 2664-2786
pISSN - 1608-9391
DOI - 10.33899/rjs.2012.44400
Subject(s) - chemistry , quinoline , hydrazine (antidepressant) , coumarin , ethyl acetoacetate , hydrate , nucleophilic substitution , medicinal chemistry , nucleophile , nucleophilic addition , organic chemistry , stereochemistry , combinatorial chemistry , catalysis , chromatography
Coumarin and its furo derivatives (psoralene and isopsoralene) are used as precursor for preparation of heterocyclic compounds. The 4-methyl-7-mthoxycoumarin, psoralene and substituted isopsoralene (II, III and IV) which are derived from 4-methyl-7hydroxycoumarin (I), when reacted with hydrazine hydrate through nucleophilic substitution reaction under basic condition give N-amino-2-quinolone and its furo derivatives (1,5 and 9) in good yields. Reaction of these compounds (1,5 and 9) with methyl acetoacetate, ethyl acetoimidate or thiosemicarbazide, a new heterocyclic compounds will be formed pyrazolo-quinoline and it is furo derivatives (2,6 and 10); 1,2,4-triazolo-quinoline and its furo derivatives (3,7 and 11) and 1,2,4- triazolo-quinoline-2-thione (4,8 and 12) respectively. The assigned structure of the prepared compounds were elucidated by the available physical and spectral methods IR, UV and 1 H-NMR.
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