G. Bruno et al., 1-ARYL-1H,3H-THIAZOLO[3,4-A]BENZIMIDAZOLE DERIVATIVES, Acta crystallographica. Section C, Crystal structure communications, 53, 1997, pp. 1337-1341
The structural features of some 1-aryl-1H,3H-thiazolo[3,4-a]benzimidaz
oles active against human immunodefiency virus (HIV) are reported. The
diffractometric analysis reveals that the title compounds, ifluorophe
nyl)-1H,3H-thiazolo[3,4-a]benzimidazole, C15H10F2N2S, ichlorophenyl)-1
H,3H-thiazolo[3,4-a]benzimidazole, C15H10Cl2N2S, and -fluorophenyl)-1H
,3H-thiazolo[3,4-a]benzimidazole, C15H10ClFN2S, all adopt a butterfly-
like conformation which appears to be particularly important for the i
nhibition of HIV-1 reverse transcriptase (RT), an enzyme which plays a
key role in the viral life-cycle.