FIELD: medicine.
SUBSTANCE: invention relates to a compound of the formula (B-I) or to its enantiomer, diastereomer or pharmaceutically acceptable salt, where X1 is SO; X2 is O; X3 is selected from a group consisting of CH, CF and N; X4, in each case, is independently selected from a group consisting of CH and N; A is selected from a group consisting of and ; R is selected from a group consisting of and ; R1 is selected from a group consisting of hydrogen, C(O)O-tert-butyl and ; R2a is hydrogen; R2b is hydrogen; R3 is selected from a group consisting of CH2C(O)OR10a, and ; R4 is ; R5 is selected from a group consisting of C(O)R9, C(O)OR10, C(O)NR10aR10b, and ; R6 is ; R7a is selected from a group consisting of hydrogen and C1-6-alkyl; R7b is selected from a group consisting of hydrogen, halogen, C1-6-alkyl, C3-7-alkyl with a branched chain, C1-6-alkoxy; R7c is selected from a group consisting of hydrogen, halogen and C1-6-alkyl; R8 is C3-7-alkyl with a branched chain; R9 is selected from a group consisting of C3-7-alkyl with a branched chain and ; R10 is selected from a group consisting of C1-6-alkyl and C3-7-alkyl with a branched chain; R10a is selected from a group consisting of hydrogen and C1-6-alkyl; R10b is selected from a group consisting of hydrogen and C1-6-alkyl; R13a, in each case, is independently selected from a group consisting of hydrogen and C3-7-alkyl with a branched chain; R13b, in each case, is hydrogen; R14a, in each case, is independently selected from a group consisting of hydrogen and C(O)O-tret-butyl; R14b, in each case, is hydrogen; X5 is selected from a group consisting of N and CR7b; n1 is equal to 1 or 2; n2 is equal to 1 or 2, and m is equal to 1. The invention also relates to a pharmaceutical composition acting as an agonist for GPR119 receptor, based on the specified compounds.
EFFECT: new compounds and a pharmaceutical composition based on them are obtained that can be used in medicine for type 2 diabetes mellitus.
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Authors
Dates
2023-04-19—Published
2017-06-08—Filed