FIELD: organic chemistry. SUBSTANCE: products: derivatives of peptides containing natural, synthetic amino acids, isoamino acids, imino acids and substituents such as: tetrahydroquinoline, pyridyl, indolyl, benzyl (substituted and nonsubstituted). naphthyl, cyclohexyl and physiologically acceptable salts also. Reagent 1: fragment containing terminal carboxy-group or its reactive derivative. Reagent 2: corresponding fragment containing free amino-group. Synthesis is carried out in solution in the presence of condensing agent using protective groups followed by if necessary deblocking and conversion of free base to its physiologically acceptable salts. Synthesized compounds were used in medicine. EFFECT: improved method of synthesis. 3 cl
Title | Year | Author | Number |
---|---|---|---|
METHOD OF INHIBITION OF RETROVIRAL PROTEASES ACTIVITY | 1991 |
|
RU2028155C1 |
ETHYLENEDIAMINE DERIVATIVES AND FXa INHIBITOR AND ANTICOAGULANT COMPRISING THEREOF | 2001 |
|
RU2268259C2 |
LIGAND CONJUGATE WITH CYTOTOXIC DRUG PREPARATION, METHOD AND APPLICATION THEREOF | 2016 |
|
RU2708461C2 |
COMPOUNDS - SULFAMATE DERIVATIVES FOR USE IN TREATING OR RELIEVING PAIN | 2014 |
|
RU2699025C1 |
DERIVATIVES OF CYCLOHEXANE OR TETRAHYDROPYRANE OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, OR HYDRATES, OR SOLVATES OF THESE COMPOUNDS, OR THEIR SALTS, INTERMEDIATE COMPOUNDS FOR THEIR SYNTHESIS AND FUNGICIDE AGENT | 1992 |
|
RU2084439C1 |
COMBINED TREATMENT BY A TOLL-LIKE RECEPTOR (TLR7) AGONIST AND A HEPATITIS B VIRUS CAPSID ASSEMBLY INHIBITOR | 2016 |
|
RU2718917C2 |
DERIVATIVES OF DIAMINES | 2002 |
|
RU2319699C2 |
HYPOGLYCAEMIC MEDICINAL AGENT COMPRISING POLYHYDROXYBUTYLPYRAZINES, NEW POLYHYDROXY-BUTYLPYRAZINES AND METHODS OF THEIR SYNTHESIS | 1998 |
|
RU2186773C2 |
DIAMINE DERIVATIVES | 2002 |
|
RU2314303C2 |
VITAMIN D PRECURSORS, METHOD FOR PREPARATION THEREOF, AND INTERMEDIATES | 2000 |
|
RU2247710C2 |
Authors
Dates
1995-11-10—Published
1990-09-26—Filed