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   <subfield code="a">The reaction between 1,2-diaminobenzimidazole and α-halocarbonyl compounds has given some novel 9-aminoimidazo [1,2-a]benzimidazoles. On treatment with nitrous acid or potassium hydroxide in DMSO, these compounds give, in addition to the deaminated compounds, 3-nitroso-derivatives of the deamination products. In the system DMSO-KOH, 9-benzylideneaminoimidazobenzimidazoles are converted smoothly into 1(9H)-imidazobenzimidazoles. It is shown that 3-nitroso-derivatives which are unsubstituted in the NH group exist predominantly in the hydroxyimino form.</subfield>
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