FIELD: medicine; pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula (I)
wherein R1 represents (1) a halogen atom, (2) a cyano group, (3) C1-4-alkyl, (4) C1-4-alkoxy or (5) C3-8-cycloalkyl, where C1-4-alkyl, C1-4-alkoxy and C3-8-cycloalkyl can be respectively and independently substituted with 1 to 3 halogen atoms and/or cyano groups; p is an integer 0–2; when p is 2, plurality of R1 may be the same or different; R2 and R3 respectively and independently represent a hydrogen atom or C1-4-alkyl; R4 represents a hydrogen atom; or R2 and R4 together with atom with which R2 and R4 are linked, may form a 5- to 8-membered nitrogen-containing saturated heterocycle; L represents (1) a bond, (2) -CRA=CRB→ or (3) -C(=O)-NRD→ (where in each group the arrow represents a binding site with the pyridine ring); RA, RB and RD respectively and independently represent a hydrogen atom or C1-4-alkyl; X1 and X2 respectively and independently represent a halogen atom that is an agonist to somatostatin receptor of subtype 2.
EFFECT: proposed is a compound having agonistic activity to somatostatin receptor and medicinal use thereof.
12 cl, 7 ex
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Authors
Dates
2018-09-07—Published
2014-09-29—Filed