RESUMO
In investigating the reactivities of aza analogues of super-electrophile 4,6-dinitrobenzofuroxan (DNBF, 1), we have found that the nitro-substituted pyridofuroxan 2 gives a remarkably stable hydrate 3 in aqueous solution (as evidenced by the requirement of ca. 50% H(2)SO(4) (H(0) approximately -3) for complete recovery of 2). The equilibrium constant K(H)()2(O) for hydration of 2 is estimated to be >/= 100, being comparable only with the K(H)()2(O) values reported for hydration of highly activated neutral polyazaaromatics such as 2- and 6-hydroxypteridines or 7-azapteridine. Interestingly, the NH group of 3 undergoes ionization at rather low pH (p = 5.79), affording an anionic hydroxy sigma-adduct 4 which is thermodynamically 10(8) times more stable than the related sigma-adduct of pteridine. The experimental evidence is that 4 is slightly more stable than the hydroxy sigma-adduct of DNBF, indicating not only that 2 ranks among the most electrophilic heteroaromatics known to date but also than an aza group may in fact be as efficient as a nitro group in promoting sigma-complex formation. 2 is also found to be a versatile Diels-Alder reagent, as a result of the low aromatic character of its six-membered ring. Upon treatment of 2 with cyclopentadiene and 2,3-dimethylbutadiene, various reactivity patterns have been observed. These led to different cycloadducts arising from normal as well as inverse electron-demand condensations involving the pyridine ring as the dienophile or the heterodiene contributor. Altogether, the results reveal major differences between the reactivity of 2 and that of DNBF, with in particular a remarkable tendency of the pyridofuroxan adducts to undergo covalent hydration, resulting in the formation of stable carbinolamines. Also noteworthy is the characterization of a diadduct which results from a Diels-Alder trapping of the o-dinitroso intermediate involved in the exchange of the 1-oxide and 3-oxide tautomers of 2.
