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Reactions of trichloromethyldialkylamines with 2-methylbenzothiazole, 2-methylbenzoxazole, and their salts

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Trichloromethyldialkylamines react with nitrogen heterocyclic compounds containing an active methyl group or with their salts to give 2-heteryl-1,1,3,3-tetrachloro-1,3-bis(dialkylamino) propanes, which are hydrolyzed by water to heterylmalonamides. Cyanine dyes containing a dimethylcarbamoyl group in the α position relative to the polymethine chain were obtained.

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Literature cited

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Communication VIII from the series “Polychloroalkylamines.” See [1] for communication VII.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 771–773, June, 1974.

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Lazukina, L.A., Kukhar', V.P. Reactions of trichloromethyldialkylamines with 2-methylbenzothiazole, 2-methylbenzoxazole, and their salts. Chem Heterocycl Compd 10, 668–670 (1974). https://doi.org/10.1007/BF00480920

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  • DOI: https://doi.org/10.1007/BF00480920

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