FIELD: medicine, pharmaceutics.
SUBSTANCE: invention refers to compounds of general formula (I) wherein R1 represents (a) C1-6alkyl optionally containing 1-3 substitutes specified in C1-6alkylcarbonyloxy, hydroxy and a halogen atom, (b) C3-6cycloalkyl, (c) phenyl or (d) mono-C1-6alkylamino; R5 represents a hydrogen atom; R6 represents a hydrogen atom; X represents an oxygen atom or a sulphur atom; m is equal to 1; the ring A is an unsaturated 5-member ring optionally containing a substitute specified in (a) C1-6alkyl optionally containing 1-3 substitutes specified in phenyl, hydroxy and a halogen atom, C1-6alkylcarbonyl, benzyloxy and pyridyl, (b) C3-6cycloalkyl, (c) phenyl or (d) C1-6alkoxy, (e) mercapto, (f) C1-6alkylthio or (g) di-C1-3alkylamino; the ring B is an unsubstituted phenyl; the ring C is a saturated or unsaturated 5-member ring optionally containing a substitute specified in C1-6alkyl and hydroxy. Also the invention refers to the intermediate compounds of formula (II) and to the pharmaceutical composition containing the compounds of formula (I) showing melatonin agonist activity.
EFFECT: preparing the compounds of formula (I) as melatonin agonists.
14 cl, 7 dwg, 2 tbl, 98 ex
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Authors
Dates
2012-07-20—Published
2007-06-18—Filed