FIELD: chemistry of amino acids. SUBSTANCE: method of synthesis of substituted amino acids of the formula (I): R-NH-XR′ where X - L-aspartic acid or L-glutamic acid residue; R′ - phenyl, pyridine or pyrimidine containing the following groups at para-position: CN, Cl, C(O)-CH3 or C(O)-NH2; R - R3-CR1R2-C(O)--group; R1 - alkyl-C1-C2, phenyl, methoxy, chloro, trihalogenmethyl; R2 - hydrogen, C1-C2-alkyl, methoxy or together with carbon to which R1 and R2 are bound form C3-C6-cycloalkyl; R3 - n-alkyl-C3-C11, alkenyl-C3-C7, cycloalkyl-C3-C7, phenyl, alkoxy-C3-C10, C3-C6-cycloalkoxy-group which can be substituted with methyl groups at two positions, phenoxy-group. Synthesis is carried out by condensation of L-aspartic or L-glutamic acid that can be protected if necessary at alpha- or beta-carboxyl-group with chloroanhydride of the formula R3-CR1R2-C(O)Cl followed by treatment of synthesized product with amine of the formula R2-NH2. EFFECT: improved method of synthesis. 12 cl, 3 tbl
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