FIELD: chemistry.
SUBSTANCE: present invention relates to a compound corresponding to the general formula I
, wherein R1 represents methyl or ethyl, n equals 1 or 2, R2 is selected from the group consisting of hydrogen, cyano, –SO2Ra, –SO2NRbRc, –C(O)Rb, phenyl, and 5– and 6–membered heteroaryl, wherein said phenyl, 5– and 6–membered heteroaryl comprises 1 to 3 heteroatoms selected from S and N, and wherein said 5– and 6–membered heteroaryl is optionally substituted by one or more substituents independently selected from R3, R3 represents a group consisting of cyano, halogen, (C1–C4)alkyl, hydroxy(C1–C4)alkyl, (C1–C4)alkoxy, –SO2Ra, and –SO2NRbRc, Ra is selected from (C1–C4)alkyl and halogen(C1–C4)alkyl, Rb and Rc are each independently selected from hydrogen, (C1–C4)alkyl, cyano(C1–C4)alkyl and cyano(C3–C6)cycloalkyl or a pharmaceutically acceptable salt thereof. Also proposed are a pharmaceutical composition and a method for preventing, treating, or alleviating psoriasis and atopic dermatitis.
EFFECT: production of new organic compounds - inhibitors of protein tyrosine kinases, such as JAK kinases.
17 cl, 1 dwg, 3 tbl, 47 ex
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Authors
Dates
2022-01-24—Published
2018-01-19—Filed