Synthesis and antimicrobial of new anthraquinone derivatives incorporating pyrazole moiety
Treatment of 2-cyano- N-(9,10-dioxo-9,10-dihydro-anthracen-2-yl)-acetamide ( 1) with phenyl isothiocyanate/dimethylsulphate afforded the corresponding ketene N, S-acetal 2 which upon treatment with hydrazine hydrate and 4-aminoantipyrine afforded the pyrazolo derivatives 3 and 4, respectively. 3-ami...
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Published in | European journal of medicinal chemistry Vol. 45; no. 5; pp. 1843 - 1848 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
PARIS
Elsevier Masson SAS
01.05.2010
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Treatment of 2-cyano-
N-(9,10-dioxo-9,10-dihydro-anthracen-2-yl)-acetamide (
1) with phenyl isothiocyanate/dimethylsulphate afforded the corresponding ketene
N,
S-acetal
2 which upon treatment with hydrazine hydrate and 4-aminoantipyrine afforded the pyrazolo derivatives
3 and
4, respectively. 3-aminopyrazole derivative
3 was utilized as key intermediate for the synthesis of pyrazolo[3,4-d]pyrimidine
5, pentaaza-as-indacene
6, triaza-cyclopenta[c]phenanthrene
7, pyrazolo[1,5-a]pyrimidine
8,
9 and (dimethyl-pyrrol-1-yl)pyrazole
10 derivatives. Furthermore, treatment of
1 with DMF/DMA gave the corresponding acrylamide derivative
11 which upon treatment with hydrazine hydrate afforded the corresponding 3-aminopyrazole derivative
12. Moreover, coupling of
1 with 4,6-dimethyl-1
H-pyrazolo[3,4-b]pyridin-3-diazonium chloride gave the hydrazone derivative
13 which upon cyclization with acetic acid afforded the corresponding pentaaza-fluorene derivative
14. Representative compounds of the synthesized products were evaluated as antimicrobial agents. Some of these compounds exhibited promising activities.
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0223-5234 1768-3254 |
DOI: | 10.1016/j.ejmech.2010.01.021 |