FIELD: chemistry.
SUBSTANCE: invention relates to a cyclic amine derivative of formula (I)
,
where R1 is an alkoxy group having 1–3 carbon atoms, any 1–3 hydrogen atoms of which are optionally replaced with a halogen atom(s); R2 is a halogen atom; R3 represents a hydrogen atom, a halogen atom or a hydroxy group; R4 is a hydrogen atom or a halogen atom; X is -C(=O)-(CH2)n-R5 or -S(=O)2-R6; n is integer from 0 to 5; R5 is a hydrogen atom, -OR7, -SR7, -S(=O)2-R7, -C(=O)-OR7, -N(R7)R8, an alkyl group having 1–3 carbon atoms, any 1–3 hydrogen atoms of which are optionally replaced with a halogen atom(s), or 5-membered ring heteroaryl group containing 1 to 4 heteroatoms independently selected from a group consisting of a nitrogen atom, an oxygen atom and a sulfur atom, any hydrogen atom(s) of which is optionally replaced by an alkyl group(s) having 1–3 carbon atoms; R6 is an alkyl group having 1–5 carbon atoms; R7 represents a hydrogen atom or an alkyl group having 1–3 carbon atoms, any 1–3 hydrogen atoms of which are optionally replaced with a halogen atom(s); and R8 represents a hydrogen atom, an alkyl group having 1–3 carbon atoms, an acyl group having 2–4 carbon atoms, or an alkylsulphonyl group having 1–3 carbon atoms, or a pharmaceutically acceptable salt thereof.
EFFECT: disclosed is a cyclic amine derivative which has retinoid orthophanic receptor antagonist activity γ and has a therapeutic effect or preventive effect on autoimmune diseases.
11 cl, 12 dwg, 3 tbl, 74 ex
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Authors
Dates
2019-08-07—Published
2017-01-27—Filed