FIELD: chemistry.
SUBSTANCE: invention relates to a method of obtaining 3-hetaryl-1,5,3-dithiazocinanes, which consists in the interaction of N1,N1,N7,N7-tetramethyl -2,6-dithiaheptane -1,7-diamine with hetarylamine in the presence of a catalyst CuCl2 in a molar ratio N1,N1,N7,N7-tetramethyl -2,6-dithiaheptane -1,7-diamine:hetarylamine:CuCl2=10:10:(0.3-0.7) at a temperature of 55-65°C and atmospheric pressure in chloroform as a solvent for 60-90 min. The output of respective 3-hetaryl-1,5,3-dithiazocinanes constitutes 68-90%. .
EFFECT: method improvement.
1 tbl, 16 ex
Title | Year | Author | Number |
---|---|---|---|
METHOD OF OBTAINING 3-HETARYL-1,5,3-DITHIAZEPINANES | 2012 |
|
RU2529502C2 |
METHOD OF OBTAINING 3-ARYL-1,5,3-DITHIAZOCANES | 2012 |
|
RU2538600C2 |
METHOD FOR PREPARING N-(1,5,3-DITHIAZOCYNAN-3-YL)AMIDES | 2012 |
|
RU2496777C2 |
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METHOD OF PRODUCING N-(1,5,3-DITHIAZEPAN-3-YL)AMIDES | 2011 |
|
RU2482114C2 |
METHOD OF PRODUCING N-CYCLOALKYL-SUBSTITUTED 1,5,3-DITHIAZEPANES | 2015 |
|
RU2601313C1 |
METHOD OF OBTAINING 3-PYRIDINYL-1,5,3-DITHIAZEPINANES | 2012 |
|
RU2532923C2 |
METHOD OF PRODUCING N-(1,5,3-DITHIAZOCYNAN-3-YL)AMIDES | 2011 |
|
RU2565788C2 |
METHOD OF PRODUCING N-ARYL-1,5,3-DITHIAZONANES | 2014 |
|
RU2559361C1 |
Authors
Dates
2014-12-20—Published
2012-10-25—Filed