FIELD: chemistry.
SUBSTANCE: invention relates to a method of obtaining 3-pyridinyl-1,5,3-dithiazepinanes of formula 
I. The essence of the method consists in the interaction of respective N,N-bis(methoxymethyl)-N-pyridinamine with 1,2-ethanedithiol in the presence of the catalyst CuCl2 in a molar ratio N-bis(methoxymethyl)-N-pyridinamine: 1,2-ethanedithiol: CuCl2=10:10:(0,3-0,7) at room temperature and atmospheric pressure in chloroform for 120-150 minutes. The output of respective 3-pyridinyl-1,5,3-dithiazepinanes of general formula (1) constitutes 68-89% 
(a); 
(b); 
(c); 
(d).
EFFECT: improvement of the method.
1 tbl
| Title | Year | Author | Number |
|---|---|---|---|
| METHOD OF OBTAINING 3-HETARYL-1,5,3-DITHIAZEPINANES | 2012 |
|
RU2529502C2 |
| METHOD OF OBTAINING 3-PYRIDINYL-1,5,3-DITHIAZOCINANES | 2012 |
|
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| METHOD OF OBTAINING 3-HETARYL-1,5,3-DITHIAZOCINANES | 2012 |
|
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|
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