FIELD: chemistry.
SUBSTANCE: invention relates to a compound of formula (I) or pharmaceutically acceptable salts thereof , in which X is -CH2- or -O-; Y is -CH2- or -CF2-; Z is -CH2- or -C(=O)-; R1 is a member selected from the group consisting of: (a) phenyl unsubstituted or substituted by one, two or three members of Ra; (b) a 5-6 membered monocyclic heteroaromatic ring having one or two heteroatoms independently selected from N, S, O, or a 8–10 membered bicyclic heteroaromatic ring, having one, two or three heteroatoms independently selected from N, S, O, each of which is unsubstituted or substituted by one, two, or three members of Rc; and (c) a 9-10 membered partially unsaturated heterocycloalkyl ring having one or two heteroatoms selected from O, wherein said ring is unsubstituted or substituted with one or more -F or -OCH3; and R2 is -C1–6alkyl; values of other radicals are given in the patent claim. Invention also relates to individual compounds selected from the group, pharmaceutical compositions, and a method of treating a neurological disorder.
EFFECT: new compounds of formula (I) having the properties of PDE2 inhibitors have been obtained.
31 cl, 1 tbl, 568 ex
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Authors
Dates
2018-06-28—Published
2015-04-22—Filed