Azo compounds deriving from amino benzoic acid anilides and acetoacetylamino-benzimidazolone

Abstract

When diazotizing a p-amino-benzoic acid anilide, the anilide nucleus of which is substituted in its para-position by carbamoyl, acetamino or chloro and coupling it onto 5-acetoacetylamino-benzimidazolone-(2) monoazo pigments are obtained having a high fastness to light, solvents, overlacquering and bleeding and a very high heat resistance.

Dependencies are inferred from the claim text.