2-Cyanobenzimidazoles 6 are readily prepared from 1,2-diaminobenzenes
4 and 4,5-dichloro-1,2,3-dithiazolium chloride 1, either directly or t
hrough thermal or acid-catalysed rearrangement of the isolated imine i
ntermediates 5; thermolysis of the imine 5b at 140-150 degrees C simul
taneously generates diatomic sulfur, S-2, as shown by its interception
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