NOVEL DERIVATIVES OF 1,2,4,5-TETRAHYDROBENZODDIAZEPIN, METHOD OF OBTAINING THEM, PHARMACOLOGICAL AGENT, METHOD OF OBTAINING SAME, APPLICATION OF SAID NOVEL DERIVATIVES IN OBTAINING THAT PHARMACOLOGICAL AGENT AND PLLICATION OF RADIOACTIVE TRACER LABELLED ANTAGONIST OF MG1UR1 RECEPTOR

摘要

The present invention is concerned with 1,2,4,5-tetrahydro-benzo[d]azepin derivatives as well as with their pharmaceutically acceptable salts in their racemic and optically active form, which compounds are antagonists at metabotropic glutamate receptors and therefore useful for the treatment of diseases related to these receptors.