FIELD: chemistry.
SUBSTANCE: present invention relates to new compounds of formula I: , where m ranges from 0 to 3, n ranges from 1 to 3, p is 0, Ar is phenyl, possibly substituted with C1-C6-alkyl, cycloalkyl, hydroxyalkyl, halogen, hydroxyl or cyano group, X is -O-,R1 and R2 each is independently hydrogen, C1-6alkyl or C1-6alkoxy-C1-6alkyl or hydroxy-C1-6alkyl, or one of R1 and R2 is hydrogen or C1-6 alkyl, and the other is C1-6alkylcarbonyl, C3-C8 cycloalkyl, aryl-C1-6alkyl or hydroxyl, or R1 and R2 together with the nitrogen atom to which they are bonded can form a three- to seven-member ring, which can possibly contain an additional N heteroatom, or R1 and R2 together with the nitrogen atom to which they are bonded can form a guanidyl group, amidinyl group, carbamyl group or urea group, each R3 is independently C1-6alkyl, R4 and R5 each is independently hydrogen or C1-6alkyl; or their pharmaceutically acceptable salts, as well as pharmaceutical compositions containing these compounds.
EFFECT: invention can selectively modulate 5-HT receptors, including 5-HT6 and 5-HT2A receptors.
17 cl, 1 tbl, 6 ex
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Authors
Dates
2009-11-10—Published
2005-04-27—Filed