FIELD: organic chemistry, pharmacy. SUBSTANCE: invention relates to a new compound - N,N-dimethyl-2-[5-(1,2,4-triazole-1-yl-methyl)-1H-indole-3-yl]-ethylamine sulfate salt (2:1) of structural formula (I) and its pharmaceutically acceptable hydrate. Method of producing salt or its hydrate involves an interaction of N,N-dimethyl-2-[5-(1,2,4-triazole-1-yl-methyl)-1H-indole-3-yl]-ethylamine of the formula (II) with about 0.5 molar equivalent sulfuric acid in a suitable solvent. Invention describes a pharmaceutical composition and a drug for treatment and/or prophylaxis of clinical states where the use of a selective agonist of 5-HT1-like receptors is indicated. N, N-Dimethyl-2-[5-(1,2,4-triazole-1-yl-methyl)-1H-indole-3-yl] -ethylamine sulfate salt is a selective agonist of 5-HT1-like receptors and therefore is benefit for treatment of patients with clinical disorders, especially migraine and related disorders, where the use of a selective agonist of these receptors is indicated. EFFECT: improved method of preparing, enhanced effectiveness of a drug proposed. 17 cl, 17 ex
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PROCESS FOR PREPARING INDOLE DERIVATIVES |
1993 |
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METHOD OF PREPARING 5-(1,2,4-TRIAZOL-1-YL)TRIPTAMINE COMPOUNDS, AND 2-[5- (1,2,4-TRIAZOL-1-YL)-1H-INDOL-3-YL]ETHANOL |
1995 |
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SUBSTITUTED MORPHOLINE DERIVATIVES, METHOD OF THEIR SYNTHESIS, PHARMACEUTICAL COMPOSITION BASED ON SAID, METHOD OF DECREASE OF TACHIKININ LEVEL IN TREATMENT OR PROPHYLAXIS OF PHYSIOLOGICAL STATES ASSOCIATED WITH TACHIKININ EXCESS |
1994 |
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3-[2-(DIMETHYLAMINO)-ETHYL]-N-METHYL-1H-INDOLE-5-METHANE SULFONEAMIDE SULFATE SALT (2:1) OR ITS PHARMACEUTICALLY ACCEPTABLE SOLVATES, METHOD OF THEIR SYNTHESIS, PHARMACEUTICAL COMPOSITIONS BASED ON THEREOF, METHOD OF HEADACHE TREATMENT |
1991 |
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PHARMACEUTICALLY ACCEPTABLE SALTS OF 2-{4-[(3S)-PIPERIDIN-3-YL]PHENYL}-2H-INDAZOLE-7-CARBOXAMIDE |
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N,N-DIMETHYL-2-(5-(2-OXO-1,3-OXAZOLIDINE-4-YL-METHYL)-1H-INDO- -LE-3-YL)-ETHYLAMINE, ITS PHYSIOLOGICALLY ACCEPTABLE SALT OR SOLVATE, METHOD OF ITS SYNTHESIS, DRUG USED AS AN AGONIST OF "5-HT-LIKE" RECEPTOR IN MAMMALS, METHOD OF DRUG AGENT PREPARING |
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SUBSTITUTED HETEROCYCLES OR THEIR PHARMACEUTICALLY ACCEPTABLE SALT, PHARMACEUTICAL COMPOSITION FOR BLOCKADE OF NEUROKININ-1 RECEPTORS IN MAMMALS, METHOD OF BLOCKADE OF NEUROKININ-1 RECEPTORS IN MAMMALS |
1993 |
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