| Title |
Year |
Author |
Number |
| BENZISOTHIAZOLE- OR BENZISOXAZOLE-3-CARBOXAMIDES OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, METHODS OF THEIR SYNTHESIS AND PHARMACEUTICAL COMPOSITION SHOWING ANTIPSYCHOTIC ACTIVITY |
1992 |
- Nikolas Dzh.Khrib[Us]
- Dzhon G.Dzhurkak[Us]
|
RU2039057C1 |
| 1-[PYRIDO(3,4-B)-1,4-OXAZINYL-4-YL]-1H-INDOLES, METHOD OF THEIR SYNTHESIS, COMPOSITION ON THEIR BASIS AND DERIVATIVE OF N-(4-PYRIDINYL)-1H-INDOLE-1-AMINE |
1992 |
- Richard Charl'Z Ehffland[Us]
|
RU2042680C1 |
| METHOD FOR PRODUCTION OF SUBSTITUTED N-(ARYL OXYALKYL)-HETEROARYL PIPERIDINE OR HETEROARYL PIPERAZINE |
1990 |
- Dzhozef Tomas Strupchevski[Us]
- Grover Kleveland Khelslej[Us]
- Julin Chiang[Us]
- Kennet Dzh.Bordeo[Us]
|
RU2062776C1 |
| SUBSTITUTED (PYRIDINYLAMINO)-BENZISOXAZOLES OR THEIR PHARMACEUTICALLY ACCEPTABLE ACID-ADDITIVE SALTS AND A METHOD OF THEIR SYNTHESIS |
1993 |
- Richard S.Ehffland[Us]
- Dzhozef T.Klejn[Us]
- Lourens L.Martin[Us]
- Gregori M.Shatske[Us]
- Kevin Dzh.Kehpplz[Us]
- Dzhon D.Tomer Iy[Us]
|
RU2083575C1 |
| [(ARYLALKYLPIPERIDINYL-4-YL)-METHYL]-2A,3,4,5-TETRAHYDRO-1-ONES OR THEIR ACID-ADDITIVE SALTS AND A METHOD OF THEIR PREPARING |
1992 |
- Rehjmond V.Kosli Ml.[Us]
- Bettina Shpal'[Us]
|
RU2043989C1 |
| METHOD OF SYNTHESIS OF AMINOCARBONYLCARBAMATES |
1990 |
- Ehdvard Dzhozef Glehmkovski[Us]
- Julin Chiang[Us]
- Rassel Richard Li Khejmer[Us]
|
RU2069664C1 |
| CARBAMIC ACID DERIVATIVES AND THEIR PHARMACEUTICALLY ACCEPTABLE ACID-ADDITIVE SALTS, METHOD OF THEIR SYNTHESIS (VARIANTS) AND PHARMACEUTICAL COMPOSITION |
1992 |
- Dehniz Mehri Flehnagan[Us]
- Lorehns Leo Martin[Us]
|
RU2103271C1 |
| DERIVATIVES OF N-(ARYLOXYALKYL)-HETEROARYLPIPERIDINE AND HETEROARYLPIPERAZINE AND PHARMACEUTICAL COMPOSITION BASED ON THEREOF |
1990 |
- Dzhozef Tomas Strupchevski
- Grover Kleveland Khelslej
- Julin Chiang
- Kennet Dzh. Bordeo
|
RU2147583C1 |
| METHOD OF SYNTHESIS OF 9-AMINO-1,2,3,4-TETRAHYDROACRIDINE |
1992 |
- Tomas Bing Kin Li[Us]
- Kejt Eh.Goring[Us]
|
RU2076099C1 |
| GALANTHAMINE DERIVATIVES AND PHARMACEUTICAL COMPOSITION |
1994 |
- Rajmond V.Koslej
- Larri Dehvis
- Veronika Taberna
|
RU2114850C1 |
where R - hydrogen, lower alkyl or a group of the formula (II) 
or (III) 
where R1-CHO or -CN. Reagent 1: compound of the formula (IV) 
where R as indicated above; R3 - benzyl. Reagent 2: halogenating agent, preferably sulfuryl chloride. Reagents 1 and 2 after interaction form compound of the formula (V) 
which is subjected for interaction with ammonia, preferably at the room temperature. Compound of the formula (IV) is synthesized from the compound of the formula (VI) 
and benzylmercaptan in the medium of aprotonic organic solvent. Synthesized products were used as intermediate compounds for synthesis of pharmaceutically active substances. EFFECT: improved method of synthesis. 6 cl
