FIELD: chemistry.
SUBSTANCE: invention relates to a piperidine derivative of formula 1, stereoisomers or pharmaceutically acceptable salts thereof. Compounds of formula 1 have GPR119 agonist properties. In formula 1 [formula 1] W is O or N-Rh group; Ra, Rb and Rh each independently is H or C1-3 alkyl group; Rc is -F or -C1-3 hyperfluoride alkyl group; Rd and Re are each independently selected from a group consisting of H, halogen, -C1-5 alkyl group; or Rd and Re are combined to form a -C3-7 cycloalkyl group; selected from a group consisting of: , where Rf1 and Rf2 are each independently H, halogen or -CN group; selected from a group consisting of: , where Rk1 and Rk2 are each independently H, -CN Group, halogen or -C1-5 alkyl(OH) group; is ; Q is H, -S(O)R1 group, -S(O)2R1 group, -C(O)R1 group, -C(O)OR1 group, -C(O)NHR1 group, -C(O)NR2R3 group, -S(O)2NHR1 group, -S(O)2NR2R3 group or . Invention also relates to a pharmaceutical composition.
EFFECT: novel piperidine derivatives of formula 1, which control GPR119 activity, are obtained.
8 cl, 183 tbl, 131 ex
Title | Year | Author | Number |
---|---|---|---|
AMIDE DERIVATIVES AS GRP119 AGONISTS | 2014 |
|
RU2642429C2 |
ARYLSULFONYLMETHYL OR ARYLSULFONAMIDE DERIVATIVES OF AROMATICS, PHARMACEUTICAL COMPOSITION BASED ON THEM AND WAY OF TREATMENT AGAINST ABNORMALITIES RESPONSIVE TO DOPAMINE D RECEPTOR LIGAND TREATMENT, WITH THEIR HELP | 2005 |
|
RU2442781C2 |
BI-ARYL-META-PYRIMIDINE KINASE INHIBITORS | 2006 |
|
RU2597364C2 |
BI-ARYL-META-PYRIMIDINE KINASE INHIBITORS | 2006 |
|
RU2589878C2 |
PYRAZOL-4-YL-HETEROCYCLYL-CARBOXAMIDE COMPOUNDS AND METHODS FOR APPLICATION | 2012 |
|
RU2638552C2 |
THIAZOLOPYRIMIDINONES AS MODULATORS OF NMDA RECEPTOR ACTIVITY | 2014 |
|
RU2703273C2 |
ISOQUINOLINONE DERIVATIVES USEFUL IN TREATING CANCER | 2015 |
|
RU2690853C2 |
NEW COMPOUNDS FOR SELECTIVE HISTONE DEACETYLASE INHIBITORS AND PHARMACEUTICAL COMPOSITION INCLUDING SUCH COMPOUNDS | 2014 |
|
RU2634694C2 |
GCN2 INHIBITORS AND THEIR USE | 2019 |
|
RU2811403C2 |
GCN2 INHIBITORS AND THEIR USE | 2019 |
|
RU2811408C2 |
Authors
Dates
2016-11-27—Published
2013-06-11—Filed