FIELD: organic chemistry, medicine, pharmacy.
SUBSTANCE: invention relates to imidazopyridine derivatives of the formula (I): that are inhibitors of proton pump. Invention describes compound of the formula (I) or its pharmaceutical acceptable salt wherein Het represents a 5-6-membered aromatic heterocyclic group comprising at least one atom of oxygen or sulfur and substituted with group R3 and group R4 at ortho-positions; R1 represents hydrogen atom (H), -CH3 or -CH2OH; R2 represents -CH3 or -CH2CH3; R3 and R4 are chosen independently from the following group: H, (C1-C6)-alkyl, hydroxylated (C1-C6)-alkyl; R5 and R6 are chosen independently from hydrogen atom, (C1-C6)-alkyl, hydroxylated (C1-C6)-alkyl, (C1-C6)-alkoxy-(C1-C6)-alkyl, hydroxylated (C1-C6)-alkoxy-(C1-C)-alkyl, either R5 and R6 can form morpholine or hydroxylated pyrrolidine in common with nitrogen atom to which they are bound; X represents -NH; R10 represents -CH2-. Also, invention describes intermediate compounds used for their synthesis. Invention provides preparing novel compounds possessing useful biological properties.
EFFECT: valuable medicinal properties of compounds and medicinal agents.
2 cl, 1 tbl, 23 ex
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Authors
Dates
2007-03-10—Published
2002-08-21—Filed