Synthesis and van Alphen–Hüttel rearrangement of substituted 3H-pyrazoles, adducts of 1,3-dipolar cycloaddition of 9-diazofluorene and diphenyldiazomethane to trimethyl(tosylethynyl)silane

Resumo

Trimethyl(tosylethynyl)silane reacted in ethyl ether at 20°С with diphenyldiazomethane affording 3Н-pyrazole, a product of 1,3-dipolar cycloaddition against Auwers rule. The reaction with 9-diazofluorene is less selective, but its regioselectivity is also governed by the steric effect of the bulky trimethylsilyl substituent at the triple bond С≡С. The adduct with diphenyldiazomethane at boiling in methanol or keeping in glacial acetic acid in the presence of a catalytic quantity of conc. H₂SO₄ undergoes the Van Alphen–Hüttel rearrangement by the migration of the phenyl substituent to the atom N² in the 1Н-pyrazole. The same 1Н-pyrazole together with a product of nitrogen elimination, trimethylsilyl substituted cyclopropane, is formed in the 2: 1 ratio at boiling in benzene. A similar behavior is observed in the glacial acetic acid for the anti-Auwers adduct of 9-diazofluorene. It suffers nitrogen elimination at boiling in benzene converting in spirocyclic cyclopropene. The Auwers adduct of 9-diazofluorene at boiling in methanol transforms due to the van Alphen–Hüttel rearrangement into the corresponding 4Н-pyrazole that undergoes a hydrodesilylation to give a derivative of 1Н-pyrazole, 3-tosyl-1(2)H-dibenzo[e,g]indazole.