Haloacetylated enol ethers. 13. Synthesis of N-[1-aryl(alkyl)-3-oxo-4,4,4-trichloro-1-buten-1-yl]-o-phenylenediamines and 2-trichloromethyl-4-aryl-3H-1,5-benzodiazepines

The synthesis and isolation of the intermediates N-[1-aryl(alkyl)-3-oxo-4,4 ,4-trichloro-1-buten-1-yl]-o-phenylenediamines 2a-f and the corresponding 2 -trichloromethyl-4-aryl-3H-1,5-benzodiazepines 3c-g or benzimidazoles 4a-b derivatives obtained from the intramolecular cyclization of 2a-f or from di rect cyclocondensation reaction of beta-alkoxyvinyl trichloromethyl ketones 1a-g with o-phenylenediamine, is reported. Depending of the structure of t he beta-alkoxyvinyl trichloromethyl ketones or the N-[1-aryl(alkyl)-3-oxo-4 ,4,4-trichloro-buten- 1-yl]-o-phenylenediamines and the reactions condition s, benzimidazoles or 3H-1,5-benzodiazepines were obtained.