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https://doi.org/10.1515/acph-2015-0037

Facile heterocyclic synthesis and antimicrobial activity of polysubstituted and condensed pyrazolopyranopyrimidine and pyrazolopyranotriazine derivatives

HEND N. HAFEZ ; Al-Imam Mohammad Ibn Saud Islamic University (IMSIU), Faculty of Science, Department of Chemistry, P.O.Box 90950 Riyadh 11623, Kingdom of Saudi Arabia; Photochemistry Department (Heterocyclic & Nucleosides Unit), National Research Centre, Cairo, Egypt
ABDULRAHMAN G. ALSHAMMARI ; Al-Imam Mohammad Ibn Saud Islamic University (IMSIU), Faculty of Science, Department of Chemistry, P.O.Box 90950 Riyadh 11623, Kingdom of Saudi Arabia
ABDEL-RHMAN B. A. EL-GAZZAR ; Al-Imam Mohammad Ibn Saud Islamic University (IMSIU), Faculty of Science, Department of Chemistry, P.O.Box 90950 Riyadh 11623, Kingdom of Saudi Arabia; Photochemistry Department (Heterocyclic & Nucleosides Unit), National Research Centre, Cairo, Egypt


Puni tekst: engleski pdf 423 Kb

str. 399-412

preuzimanja: 1.320

citiraj


Sažetak

Reaction of 6-amino-3-methyl-4-(substituted phenyl)-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile (1) with triethylorthoformate followed by treatment with hydrazine hydrate, formic acid, acetic acid, phenylisocyanate, ammonium thiocyanate and formamide afforded the corresponding pyranopyrimidine derivatives 2–6. Cyclocondensation of 1 with cyclohexanone afforded pyrazolopyranoquinoline 7. One-pot process of diazotation and de-diazochlorination of 1 afforded pyrazolopyranotriazine derivative 8, which upon treatment with secondary amines afforded 9 and 10a-c. Condensation of 2 with aromatic aldehyde gave the corresponding Schiff bases 11a,b, the oxidative cyclization of the hydrazone with appropriate oxidant afforded 11-(4-fluorophenyl))-2-(4-substitutedphenyl)-10-methyl-8,11-dihydropyrazolo-[4',3':5,6]pyrano[3,2-e][1,2,4]triazolo[1,5-c]pyrimidines (12a,b). Structures of the synthesized compounds were confirmed by spectral data and elemental analysis. All synthesized compounds were evaluated for antibacterial and antifungal activities compared to norfloxacin and fluconazole as standard drugs. Compounds 9, 10c, 12a and 15 were found to be the most potent antibacterial agents, with activity equal to that of norfloxacin. On the other hand, compound 5 exhibited higher antifungal activity compared to fluconazole.

Ključne riječi

pyrazolopyranopyrimidine; pyrazolopyranotriazine; pyrazolopyranoquinoline; antimicrobial activity

Hrčak ID:

144157

URI

https://hrcak.srce.hr/144157

Datum izdavanja:

31.12.2015.

Posjeta: 2.010 *