FIELD: medicine, pharmaceutics.
SUBSTANCE: invention related to a spiro amino compound of formula
,
wherein m represents 1 or 2 or 3, n represents 1 or 2, R is specified in a 6-merous aromatic ring and a 5-merous heteroaromatic ring containing 1 to 2 heteroatoms specified in S and N; this ring is substituted by one or two substitutes specified in a group consisting of (C1-C3)alkyl, halogen atom, (C3-C5)cycloalkyloxygroup, phenyl optionally substituted by one or more halogen atoms, 5- or 6-merous heterocycle containing at least one nitrogen atom specified in 1,2,3-triazole, pyrimidine, pyridine, and pyrazine; P represents a substitute Q, wherein Q is specified in a group consisting of phenyl, pyridyl, pyrimidyl; Q is optionally substituted by one or more substitutes specified in a group consisting of (C1-C3)alkyl, halogen, trifluoromethyl, methylcarboxygroup. The invention also refers to a spiro amino compound of formula (VI), wherein m represents 1 or 3, n represents 1 or 2, R represents phenyl substituted by the substitute cyclopropyl (C1-C3)alkoxy, P represents a substitute Q, wherein Q is specified in a group consisting of phenyl, pyridyl, pyrimidinyl; Q is optionally substituted by one or more substitutes specified in a group consisting of (C1-C3)alkyl, halogen, trifluoromethyl and methylcarboxygroup. The compounds of formula IV are applicable to produce a drug preparation for treating the pathologies, which require an orexin receptor 1 antagonist to be applied.
EFFECT: spiro amino compounds possessing the orexin receptor agonist activity.
19 cl, 99 ex
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Authors
Dates
2015-09-10—Published
2010-07-15—Filed