Pregled bibliografske jedinice broj: 626959
Synthesis of 9-Sulfonylpurine Derivatives and Stability Enhancement with Small Structural Modifications
Synthesis of 9-Sulfonylpurine Derivatives and Stability Enhancement with Small Structural Modifications // XXIII. Hrvatski skup kemičara i kemijskih inženjera, Knjiga sažetaka / Hadžiev, Andrea ; Blažeković, Zdenko (ur.).
Zagreb: Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2013. str. 42-42 (predavanje, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 626959 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis of 9-Sulfonylpurine Derivatives and Stability Enhancement with Small Structural Modifications
Autori
Saftić, Dijana ; Matić, Josipa ; Ban, Željka ; Ismaili, Hamit ; Žinić, Biserka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
XXIII. Hrvatski skup kemičara i kemijskih inženjera, Knjiga sažetaka
/ Hadžiev, Andrea ; Blažeković, Zdenko - Zagreb : Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2013, 42-42
ISBN
978-953-6894-50-5
Skup
XXIII. Hrvatski skup kemičara i kemijskih inženjera
Mjesto i datum
Osijek, Hrvatska, 21.04.2013. - 24.04.2013
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Domaća recenzija
Ključne riječi
Purini ; sulfonil- derivati ; sulfonilpurinski derivati
(Purines ; Sulfonyl- Derivatives ; Sulfonylpurine Derivatives)
Sažetak
In continuation of our previous work on the synthesis and characterization of biologically active nucleobase derivatives, here we report on the synthesis of novel N-9-sulfonyl purine derivatives. Novel 6-chloro-N-9-sulfonyl purine derivatives I were prepared by the condensation reaction of 6-chloropurine with different sulfonyl chlorides in acetone and in the presence of aqueous KOH at 0 oC. The sulfonylation reaction occurred regioselectively at the purine N9 position lacking any concurrent N7 sulfonylation, as proved by the spectral data. It has been observed that all obtained compounds of type I tend to degrade in solution into starting 6-chloropurine and respective sulfonic acid. Degradation was determined by 1H NMR. It has been concluded that electronic effects of chloro-substituent at purine C-6 position may destabilize the N-S bond. Therefore, chlorine was substituted by electron-donating morfolino group giving II with dramatically increased stability in solution as determined by time-dependent 1H-NMR experiments. The latter reaction opens the way toward a new series of various 6-amino substituted N-9-sulfonylpurines II with increased stability which enables the assessment of their potential anticancer activity by systematic in vitro screening on tumor and normal human cells.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
098-0982914-2935 - Sinteza novih biološki aktivnih derivata nukleobaza i nukleotida (Žinić, Biserka, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Željka Ban
(autor)
Josipa Matić
(autor)
Dijana Pavlović Saftić
(autor)
Biserka Žinić
(autor)