FIELD: chemistry.
SUBSTANCE: invention concerns single-stage method of obtaining fructopiranose sulfamate derivatives of the general formula (I) , where X is selected out of CH2 or O; R3, R4, R5 and R6, each selected independently out of hydrogen or low-grade alkyl, then X is CH2, R5 and R6 can be alkene groups linked with formation of benzene ring, then X is O, R3 and R4 and/or R5 and R6 together can be methylenedioxy group of the formula: , where R7 and R8 are equal or different and denote hydrogen, low-grade alkyl, or are an alkyl and are linked together to form cyclopentyl or cyclohexyl ring; , involving reaction of compound of the formula (II) with sulfuryldiamide at high temperature in the presence of 0 to ca. 10% of water, resulting in obtaining of respective compound of the formula (I); and method of obtaining compound of the formula (1a).
EFFECT: development of a single-stage method for obtaining fructopiranose sulfamate derivatives.
29 cl, 10 tbl, 10 ex
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Authors
Dates
2008-09-10—Published
2004-03-02—Filed