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Synthesis of 1,2-diamino imidazole derivatives by the reaction of benzaldehyde guanylhydrazone with α-haloalkyl aryl ketones
Authors:A V Ivashchenko  V T Lazareva  E K Prudnikova  S P Ivashchenko  V G Rumyantsev
Institution:(1) Scientific-Research Institute of Organic Intermediates and Dyes, 103787 Moscow
Abstract:2-Amino-1-benzylideneamino-4-arylimidazoles were obtained by the reaction of benzaldehyde guanylhydrazone with 4-alkyl- and 4-aryl-OHgr-haloacetophenones. Side products of this reaction were cis- and trans-1,1prime-bis(benzylideneamino)-4,4prime-diaryl-2,2prime-azoimidazoles. The corresponding 2-amino-1-benzylideneaminoimidazole and 1-benzyl-ideneaminoimidazol,2-a]imidazole were obtained in the reaction of agr-bromopropiophenone with benzaldehyde guanylhydrazone. The 2-amino-1-benzylideneamino-4-arylimidazoles were converted by successive reactions to 1,2-diatnino-4-arylimidazoles and then to imidazo1,2-b]-1,2,4-triazine derivatives —dyes for liquid crystals with positive dichroism.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 236–241, February, 1982.
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