| Title |
Year |
Author |
Number |
| METHOD OF SYNTHESIS OF AROMATIC DERIVATIVES OR THEIR SALTS WITH ORGANIC OR INORGANIC ACIDS OR THEIR RACEMATES |
1990 |
- Ksav'E Ehmon-Al'T[Fr]
- P'Er Guljauik[Fr]
- Vinchentso Proietto[It]
- Did'E Van Bruk[Be]
|
RU2084453C1 |
| 4-ALKYLENEPIPERIDINE DERIVATIVES OR THEIR SALTS WITH MINERAL OR ORGANIC ACIDS, OR QUATERNARY AMMONIUM SALTS SHOWING ACTIVITY WITH RESPECT TO NEUROKININ SYSTEM, A METHOD OF THEIR SYNTHESIS AND PHARMACEUTICAL COMPOSITION |
1992 |
- Ksav'E Ehmond-Al'T[Fr]
- Izabell' Grossriete[Fr]
- Vensanzo Pruaetto[It]
- Did'E Van Broekk[Be]
|
RU2099327C1 |
| POLYCYCLIC AMINE-CONTAINING COMPOUNDS OR THEIR SALTS, THEIR OPTICALLY PURE ISOMERS, METHOD OF SYNTHESIS OF POLYCYCLIC AMINE-CONTAINING COMPOUNDS, CYCLIC AMINE-CONTAINING COMPOUNDS OR THEIR SALTS, THEIR OPTICALLY PURE ISOMERS AND PHARMACEUTICAL COMPOSITION SHOWING ANTAGONISTIC ACTIVITY WITH RESPECT TO NEUROKININ RECEPTORS |
1992 |
- Ksav'E Ehmond-Al'T[Fr]
- Patrik Gel'[Fr]
- Vensanzo Pruaetto[It]
- P'Er Gulauik[Fr]
|
RU2083574C1 |
| METHOD OF SYNTHESIS OF (-)-N-METHYL-N-[4-(PHENYL-4-ACETAMINOPIPERIDINE-1-YL)-2-(3,4- -DICHLOROPHENYL)-BUTYL]-BENZAMIDE AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS |
1995 |
- Marsel' Deskamp[Be]
- Zhoehl' Radisson[Fr]
- Zhill' Ann-Arshar[Fr]
|
RU2097376C1 |
| ENANTIOMERS OF AROMATIC NITROGEN-CONTAINING DERIVATIVES AND THEIR SALTS WITH INORGANIC OR ORGANIC ACIDS AND A METHOD OF THEIR SYNTHESIS |
1990 |
- Ksav'E Ehmon-Al'T
- P'Er Guljauik
- Vinchentso Proietto
- Did'E Van Bruk
|
RU2114828C1 |
| DERIVATIVES OF PIPERIDINE, THEIR SALTS, METHODS OF THEIR SYNTHESIS, PHARMACEUTICAL COMPOSITION BASED ON THEREOF AND INTERMEDIATE SUBSTANCES |
1995 |
- Daniel' Bishon
- Patrik Gele
- Did'E Van Broskk
- Ksav'E Ehmond-Al'T
- Vensanzo Pruaetto
|
RU2143425C1 |
| N-ALKYLENEPIPERIDINE DERIVATIVES, METHOD OF THEIR SYNTHESIS, PHARMACEUTICAL COMPOSITION BASED ON THEREOF, OPTICALLY PURE DERIVATIVES OF N-ALKYLENEPIPERIDINE |
1992 |
|
RU2089547C1 |
| BASIC TYPE TERTIARY AMIDES, METHODS OF PREPARING THEREOF, AND PHARMACEUTICAL COMPOSITION COMPRISING SAID COMPOUNDS |
1993 |
- Ksav'E Ehmon-Al'T
- Patrik Gejl'
- Vinchentso Proietto
- Didier Van Broek
|
RU2120436C1 |
| SUBSTITUTED HETEROCYCLIC COMPOUNDS, METHOD OF THEIR SYNTHESIS AND PHARMACEUTICAL COMPOSITION |
1996 |
- Ksav'E Ehmon-Al'T
- Izabell' Grossrieter
- Patrik Gel'
- Vinchentso Proietto
- Did'E Van Bruk
|
RU2157807C2 |
| N-SUBSTITUTED HETEROCYCLIC DERIVATIVES OR THEIR SALTS, INTERMEDIATE DERIVATIVES OF PYRIMIDINE AND IMIDAZOLINE AND A PHARMACEUTICAL COMPOSITION BASED ON THE SUBSTITUTED HETEROCYCLIC DERIVATIVES |
1991 |
- Klod Bernar[Fr]
- Zhan-Klod Brel'Er[Fr]
- Zhak Kleman[Fr]
- Dino Nisato[It]
- P'Er Perro[Fr]
|
RU2099331C1 |
where Y - group Cy-
where Cy - unsubstituted phenyl or phenyl substituted with hydroxyl, C1-C4-alkoxy-group, C3-C6-cycloalkyl, pyrimidyl; Ar' - unsubstituted or substituted phenyl; R - hydrogen, C1-C3-alkyl; T - group -CO- or -CONH; m = 2 or 3; Z - M or OM where M - C1-C4-alkyl. Reagent 1: compound of the formula (II) 
where m, Ar' and R - as indicated above; E - O-protective group. Reagent 2: HCO-Z or O=C=N=Z. Synthesized compounds were used in medicine as antagonists of neurokinine A receptors. EFFECT: improved method of synthesis. 11 cl, 13 tbl, 75 ex