FIELD: chemical or physical processes.
SUBSTANCE: invention relates to synthetic synthesis of compound of formula (I), which includes two successive steps (b1) and (b2) in accordance with principles of single-reactor synthesis. Step (b1) comprises reacting a compound of formula (II) with a compound of formula Z-Sp-A (III) in the presence of at least one polar solvent, at least one base at temperature T1 from 70 to 150 °C in order to form ether. At step (b2), said ether is reacted with aqueous hydroxylamine solution at temperature T2 from 30 to 70 °C. In said formulas, A is a binding group, selected from a group of imidazolidinyl, thioimidazolidinyl, triazoyl, trithioazoyl, ureyl, thioureyl, bis-ureyl, bis-thioureyl, ureidopyrimidyl and thioureidopyrimidyl or a group corresponding to formula (IV): -C(OR2)=O (IV), where R2 is a carbon group containing 1 to 20 carbon atoms and optionally containing at least one heteroatom; R1 is C1-C12 alkyl group or OR', where R' is C1-C12 alkyl group; n is integer from 0 to 4; Sp is a linear or branched C1-C24 alkylene chain optionally interrupted by one or more nitrogen or oxygen atoms; Z—nucleofug.
(I)
(II).
EFFECT: disclosed method reduces the number of steps without detriment to purity of target oximes and without reducing their output.
23 cl, 3 ex
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Authors
Dates
2020-04-28—Published
2016-06-23—Filed