Heterocyclic compound
    5.
    发明授权
    Heterocyclic compound 有权
    杂环化合物

    公开(公告)号:US09156837B2

    公开(公告)日:2015-10-13

    申请号:US14235992

    申请日:2012-07-27

    摘要: A heterocyclic compound having an RORγt inhibitory activity, which is a compound of formula (I) or a salt thereof is provided. The compound has ring A, which is an optionally substituted cyclic group and is bound to a pyrazole ring though Q. Q is a bond, optionally substituted C1-10 alkylene, optionally substituted C2-10 alkenylene, or optionally substituted C2-10 alkynylene. R1 is a substituent. Ring B is a thiazole ring, an isothiazole ring or a dihydrothiazole ring, each of which is optionally further substituted by a substituent in addition to R2. R2 is an optionally substituted cyclyl-carbonyl-C1-6 alkyl group, an optionally substituted aminocarbonyl-C1-6 alkyl group, an optionally substituted cyclyl-C1-6 alkyl group, an optionally substituted cyclyl-C1-6 alkylamino-carbonyl group, an optionally substituted aminocarbonyl-C2-6 alkenyl group, an optionally substituted C1-6 alkylcarbonylamino-C1-6 alkyl group, an optionally substituted cyclyl-aminocarbonyl group, an optionally substituted cyclyl-carbonyl group or an optionally substituted non-aromatic heterocyclic group.

    摘要翻译: 提供具有RORγt抑制活性的杂环化合物,其为式(I)化合物或其盐。 该化合物具有环A,其为任选取代的环状基团,并且通过Q键合至吡唑环。Q为键,任选取代的C 1-10亚烷基,任选取代的C 2-10亚烯基或任选取代的C 2-10亚炔基。 R1是取代基。 环B是噻唑环,异噻唑环或二氢噻唑环,除了R2之外,它们各自任选进一步被取代基取代。 R 2是任选取代的环羰基-C 1-6烷基,任选取代的氨基羰基-C 1-6烷基,任选取代的环C 1-6烷基,任选取代的环C 1-6烷基氨基羰基, 任选取代的氨基羰基-C 2-6烯基,任选取代的C 1-6烷基羰基氨基-C 1-6烷基,任选取代的环 - 氨基羰基,任选取代的环羰基或任选取代的非芳族杂环基。

    HETEROCYCLIC COMPOUND
    7.
    发明申请
    HETEROCYCLIC COMPOUND 有权
    杂环化合物

    公开(公告)号:US20140163001A1

    公开(公告)日:2014-06-12

    申请号:US14235992

    申请日:2012-07-27

    摘要: Provided is a heterocyclic compound having an RORγt inhibitory activity. A compound represented by the formula (I): wherein ring A is an optionally substituted cyclic group, Q is a bond, optionally substituted C1-10 alkylene, optionally substituted C2-10 alkenylene, or optionally substituted C2-10 alkynylene, R1 is a substituent, ring B is a thiazole ring, an isothiazole ring or a dihydrothiazole ring, each of which is optionally further substituted by a substituent in addition to R2, and R2 is an optionally substituted cyclyl-carbonyl-C1-6 alkyl group, an optionally substituted aminocarbonyl-C1-6 alkyl group, an optionally substituted cyclyl-C1-6 alkyl group, an optionally substituted cyclyl-C1-6 alkylamino-carbonyl group, an optionally substituted aminocarbonyl-C2-6 alkenyl group, an optionally substituted C1-6 alkylcarbonylamino-C1-6 alkyl group, an optionally substituted cyclyl-aminocarbonyl group, an optionally substituted cyclyl-carbonyl group or an optionally substituted non-aromatic heterocyclic group, or a salt thereof.

    摘要翻译: 提供具有RORγt抑制活性的杂环化合物。 由式(I)表示的化合物:其中环A是任选取代的环状基团,Q是键,任选取代的C 1-10亚烷基,任选取代的C 2-10亚烯基或任选取代的C 2-10亚炔基,R 1是 取代基,环B是噻唑环,异噻唑环或二氢噻唑环,其中R 2独立地任选被取代基任意地进一步被R 2取代,R 2是任选取代的环羰基-C 1-6烷基,任选地 取代的氨基羰基-C 1-6烷基,任选取代的环烷基-C 1-6烷基,任选取代的环基-C 1-6烷基氨基 - 羰基,任选取代的氨基羰基-C 2-6链烯基,任选取代的C 1-6 烷基羰基氨基-C 1-6烷基,任选取代的环 - 氨基羰基,任选取代的环羰基或任选取代的非芳族杂环基,或其盐。