FIELD: chemistry.
SUBSTANCE: invention relates to a method of producing 2,3-dihydro[1,3]tellurazolo[3,2-α]pyrimidinium chlorides of general formula , where R1 is an alkyl or phenyl, R2 is an alkyl, phenyl or hydrogen, R1+R2 is cycloalkyl. The method includes reacting the corresponding olefin with 4,6-dimethyl-2-pyrimidine tellurenylchloride hydrochloride in equimolar ratio in an acetonitrile medium.
EFFECT: invention enables to obtain novel compounds which can be used in fine organic synthesis, in production of medicinal drugs and biologically active substances.
4 ex
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Authors
Dates
2014-09-27—Published
2013-05-21—Filed