FIELD: organic chemistry. SUBSTANCE: product: derivatives of thiazolidine carboxylic acid amides of the general formula where R1 or R2 - hydrogen or pyridyl which is unsubstituted or C1-C4-substituted; R3 - hydrogen, C1-C4-alkyl, C1-C4-alkoxycarbonyl; R4 - hydrogen, C1-C4-alkyl; A - A-C2-C7-alkylene or alkylidene; Z - group , , , which can contain substituent C1-C4-alkyl at carbon atom of ring; R5 and R6 are similar or different and every - phenyl which can be substituted with halogen or halogen-C1-C4-alkyl, or unsubstituted aromatic 5- or 6-member heterocyclic group containing nitrogen or sulfur as heteroatom; E - bond or oxygen atom, or their pharmaceutically acceptable salts. Reagent 1: acid of the formula where R1-R3 as indicated above or its reactive derivative. Reagent 2: amine of the formula ZANHR4 where radical meanings were indicated above. Reaction conditions: removal of protecting group if necessary, isolation in the form of salt if it is required. Synthesized compounds were used in medicine. EFFECT: improved method of synthesis. 11 cl, 3 tbl
Title | Year | Author | Number |
---|---|---|---|
METHOD OF SYNTHESIS OF N-ACRYLOYLPIPERAZINE DERIVATIVES | 1990 |
|
RU2024513C1 |
ACYLATED HETEROALICYCLIC DERIVATIVES, MEDICINAL AGENT SHOWING SELECTIVE ANTAGONISTIC ACTIVITY AGAINST NK-RECEPTORS, METHOD OF PROPHYLAXIS OR TREATMENT OF PATIENTS | 1998 |
|
RU2174122C1 |
BENZOPYRAN DERIVATIVES OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, AND A METHOD OF THEIR SYNTHESIS | 1991 |
|
RU2038354C1 |
α, ω-DIARYL ALKANES AND METHOD FOR THEIR PRODUCTION | 1993 |
|
RU2105752C1 |
DERIVATIVES OF SPIROPIPERIDINE, MEDICINAL AGENT, METHOD OF PROPHYLAXIS OR TREATMENT | 1999 |
|
RU2184735C2 |
COMPOUND SALTS, MEDICINAL AGENT, COMPOSITION, METHOD OF PROPHYLAXIS, METHOD OF TREATMENT | 1998 |
|
RU2190615C2 |
LIPID ANALOGS OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS | 1992 |
|
RU2076107C1 |
AZASTEROIDAL COMPOUNDS | 1991 |
|
RU2070204C1 |
NEURAMINIC ACID DERIVATIVES OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, OR THEIR ESTERS AND A PHARMACEUTICAL COMPOSITION EXHIBITING SIALIDASE-INHIBITING ACTIVITY | 1997 |
|
RU2124509C1 |
METHOD OF SYNTHESIS OF OPTICALLY ACTIVE INDOLOBENZOQUINOLINE DERIVATIVE OT ITS PHARMACEUTICALLY ACCEPTABLE SALTS | 1990 |
|
RU2045528C1 |
Authors
Dates
1995-03-10—Published
1991-06-26—Filed