Substituted 2-pyrimidinyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one and 7-pyrimidinyl-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)one derivatives
    1.
    发明公开
    Substituted 2-pyrimidinyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one and 7-pyrimidinyl-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)one derivatives 审中-公开
    取代基2-嘧啶基-6,7,8,9-四氢-1,2-嘧啶-4-酮和7-嘧啶基-2,3-二氢咪唑并[1,2-a嘧啶-5(1H)

    公开(公告)号:EP1340760A1

    公开(公告)日:2003-09-03

    申请号:EP02290488.2

    申请日:2002-02-28

    CPC分类号: C07D487/04

    摘要: The invention relates to a pyrimidone derivative represented by formula (I) or a salt thereof:
    wherein:

    X represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C 1-2 alkyl group and a hydrogen atom;
    Y represents a bond, a ethenylene group, a ethynylene group, an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxide group, a carbonyl group, a nitrogen atom being optionally; or a methylene group optionally substituted;
    R1 represents a pyrimidine group optionally substituted;
    R2 may represent a C 1-6 alkyl group optionally substituted by a C 6,10 aryloxy or a C 6,10 arylamino group ; a C 3-6 cycloalkyl group, a C 1-4 alkylthio group, a C 1-4 alkoxy group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a phenylthio group, a benzyl group, a phenyl ring, an indanyl ring, a 5,6,7,8-tetrahydronaphthyl ring, a naphthyl ring, a pyridine ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ;
    R3 and R4 represents each independently a hydrogen atom, C 1-6 alkyl group, a hydroxy group, a C 1-4 alkoxy group or a halogen atom;
    R5 represents a hydrogen atom, a C 1-6 alkyl group or a halogen atom;
    The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β or GSK3β and cdk5/p25, such as Alzheimer disease.

    摘要翻译: 本发明涉及由式(I)表示的嘧啶酮衍生物或其盐:其中:X表示两个氢原子,硫原子,氧原子或C 1-2烷基和氢原子; Y表示键,亚乙烯基,亚乙炔基,氧原子,硫原子,磺酰基,亚砜基,羰基,任选的氮原子; 或任选取代的亚甲基; R1表示任选取代的嘧啶基团; R 2可以表示任选被C 6-10芳氧基或C 6,10芳基氨基取代的C 1-6烷基; C3-6环烷基,C1-4烷硫基,C1-4烷氧基,C1-2全卤代烷基,C1-3卤代烷基,苯硫基,苄基,苯环,茚满基环 5,6,7,8-四氢萘基环,萘环,吡啶环,吡咯环,噻吩环,呋喃环或咪唑环; R3和R4各自独立地表示氢原子,C1-6烷基,羟基,C1-4烷氧基或卤素原子; R5表示氢原子,C1-6烷基或卤素原子; 本发明还涉及包含所述衍生物或其盐作为活性成分的药物,其用于预防和/或治疗由GSK3β或GSK3β和cdk5 / p25的异常活性引起的神经退行性疾病,例如 阿尔茨海默病。

    Heteroaryl substituted 2-pyrimidinyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one and 7-pyrimidinyl-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)one derivatives
    2.
    发明公开
    Heteroaryl substituted 2-pyrimidinyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one and 7-pyrimidinyl-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)one derivatives 审中-公开
    杂芳基取代基2-嘧啶基-6,7,8,9-四氢嘧啶并[1,2-a嘧啶-4-基]和7-嘧啶基-2,3-二氢咪唑并[1,2-a嘧啶-5(1H)

    公开(公告)号:EP1348708A1

    公开(公告)日:2003-10-01

    申请号:EP02290486.6

    申请日:2002-02-28

    CPC分类号: C07D487/04

    摘要: The invention relates to a pyrimidone derivative represented by formula (I) or a salt thereof wherein:


    X represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C 1-2 alkyl group and a hydrogen atom;
    Y represents a bond, an ethenylene group, an ethynylene group or a methylene group optionally substituted by one or two groups chosen from a C 1-6 alkyl group, a hydroxy group or a C 1-4 alkoxy group;
    R1 represents a 2, 4 or 5-pyrimidine ring optionally;
    R2 represents a heterocyclic bicyclic rings, having 1-4 heteroatoms selected from an oxygen atom, a sulfur atom and a nitrogen atom and having 5-9 carbon atoms, of formula

    R3 represents a hydrogen atom, a C 1-6 alkyl group, a hydroxy group, a C 1-4 alkoxy group or a halogen atom;
    R4 represents a hydrogen atom, a C 1-6 alkyl group, a C 1-4 alkoxy group or a halogen atom;
    The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β or GSK3β and cdk5/p25, such as Alzheimer disease.

    摘要翻译: 本发明涉及由式(I)表示的嘧啶酮衍生物或其盐,其中:X表示两个氢原子,硫原子,氧原子或C 1-2烷基和氢原子; Y表示任选被一个或两个选自C 1-6烷基,羟基或C 1-4烷氧基的基团取代的键,亚乙烯基,亚乙炔基或亚甲基; R1代表任选的2,4或5-嘧啶环; R 2表示具有1-4个选自氧原子,硫原子和氮原子并且具有5-9个碳原子的杂原子的杂环二环,式 R 3表示氢原子,C 1-6烷基 ,羟基,C 1-4烷氧基或卤素原子; R4表示氢原子,C1-6烷基,C1-4烷氧基或卤素原子; 本发明还涉及包含所述衍生物或其盐作为活性成分的药物,其用于预防和/或治疗由GSK3β或GSK3β和cdk5 / p25的异常活性引起的神经退行性疾病,例如 阿尔茨海默病。

    Heteroaryl substituted 2-pyridinyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one and 7-pyridinyl-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)one derivatives
    3.
    发明公开
    Heteroaryl substituted 2-pyridinyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one and 7-pyridinyl-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)one derivatives 审中-公开
    杂芳基取代基2-吡啶基-6,7,8,9-四氢-1,2-a吡啶-4-酮和7-吡啶基-2,3-二氢咪唑并[1,2-a嘧啶-5(1H)

    公开(公告)号:EP1340758A1

    公开(公告)日:2003-09-03

    申请号:EP02290485.8

    申请日:2002-02-28

    CPC分类号: C07D487/04

    摘要: The invention relates to a pyrimidone derivative represented by formula (I) or a salt thereof wherein:


    X represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C 1-2 alkyl group and a hydrogen atom;
    Y represents a bond, an ethenylene group, an ethynylene group or a methylene group optionally substituted;
    R1 represents a 2, 3 or 4-pyridine ring optionally substituted;
    R2 represents a heterocyclic bicyclic rings, having 1-4 heteroatoms selected from an oxygen atom, a sulfur atom and a nitrogen atom and having 5-9 carbon atoms, of formula

    R3 represents a hydrogen atom, a C 1-6 alkyl group, a hydroxy group, a C 1-4 alkoxy group or a halogen atom;
    R4 represents a hydrogen atom, a C 1-6 alkyl group, a C 1-4 alkoxy group or a halogen atom;
    The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β or GSK3β and cdk5/p25, such as Alzheimer disease.

    摘要翻译: 本发明涉及由式(I)表示的嘧啶酮衍生物或其盐,其中:X表示两个氢原子,硫原子,氧原子或C 1-2烷基和氢原子; Y表示键,亚乙烯基,亚乙炔基或任选取代的亚甲基; R1表示任选取代的2,3或4-吡啶环; R 2表示具有1-4个选自氧原子,硫原子和氮原子并且具有5-9个碳原子的杂原子的杂环二环,式 R 3表示氢原子,C 1-6烷基 ,羟基,C 1-4烷氧基或卤素原子; R 4表示氢原子,C 1-6烷基,C 1-4烷氧基或卤素原子; 本发明还涉及包含所述衍生物或其盐作为活性成分的药物,其用于预防和/或治疗由GSK3β或GSK3β和cdk5 / p25的异常活性引起的神经退行性疾病,例如 阿尔茨海默病。

    Substituted 2-pyridinyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one and 7-pyridinyl-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)one derivatives
    4.
    发明公开
    Substituted 2-pyridinyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one and 7-pyridinyl-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)one derivatives 审中-公开
    取代基2-吡啶基-6,7,8,9-四氢嘧啶并[1,2-a嘧啶-4-基]和7-吡啶基-2,3-二氢咪唑并[1,2-a嘧啶-5(1H)

    公开(公告)号:EP1340761A1

    公开(公告)日:2003-09-03

    申请号:EP02290489.0

    申请日:2002-02-28

    CPC分类号: C07D487/04

    摘要: The invention relates to a pyrimidone derivative represented by formula (I) or a salt thereof wherein:


    X represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C 1-2 alkyl group and a hydrogen atom;
    Y represents a bond, an ethenylene group, an ethynylene group, an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxide group, a carbonyl group, a hydroxyiminomethylene group, a dioxolan group, a nitrogen atom being optionally substituted; or a methylene group optionally substituted;
    R1 represents a 2, 3 or 4-pyridine ring optionally substituted;
    R2 may represent a C 1-6 alkyl group optionally; a C 3-6 cycloalkyl group, a C 1-4 alkylthio group, a C 1-4 alkoxy group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a phenylthio group, a benzyl group, a phenyl ring, a 5,6,7,8-tetrahydronaphthyl ring, a naphthyl ring, a pyridine ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ;
    R3 and R4 represents, each independently, a hydrogen atom, a C 1-6 alkyl group, a hydroxy group, a C 1-4 alkoxy group or a halogen atom;
    R5 represents a hydrogen atom, a C 1-6 alkyl group or a halogen atom; with the proviso that when R3 and R4 represent each a hydrogen atom then R5 is not a hydrogen atom.
    The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β or GSk3β and cdk5/p25, such as Alzheimer disease.

    摘要翻译: 本发明涉及由式(I)表示的嘧啶酮衍生物或其盐,其中:X表示两个氢原子,硫原子,氧原子或C 1-2烷基和氢原子; Y表示键,亚乙烯基,亚乙炔基,氧原子,硫原子,磺酰基,亚砜基,羰基,羟基亚氨基亚甲基,二氧戊环,任选取代的氮原子; 或任选取代的亚甲基; R1表示任选取代的2,3或4-吡啶环; 任选地,R 2可以表示C 1-6烷基; C 3-6环烷基,C 1-4烷硫基,C 1-4烷氧基,C1-2全卤代烷基,C 1-3卤代烷基,苯硫基,苄基,苯环, 5,6,7,8-四氢萘基环,萘环,吡啶环,吡咯环,噻吩环,呋喃环或咪唑环; R 3和R 4各自独立地表示氢原子,C 1-6烷基,羟基,C 1-4烷氧基或卤素原子; R5表示氢原子,C1-6烷基或卤素原子; 条件是当R 3和R 4各自表示氢原子时,R 5不是氢原子。 本发明还涉及包含所述衍生物或其盐作为活性成分的药物,其用于预防和/或治疗由GSK3β或GSk3β和cdk5 / p25的异常活性引起的神经变性疾病的预防和/或治疗,例如 阿尔茨海默病。

    2-pyrimidinyl-6,7,8,9-tetrahydropyrimido[1,2-a]Pyrimidin-4-one and 7-Pyrimidinyl-2,3-Dihydroimidazo[1,2-a]Pyrimidin-5(1H)one derivatives
    5.
    发明公开
    2-pyrimidinyl-6,7,8,9-tetrahydropyrimido[1,2-a]Pyrimidin-4-one and 7-Pyrimidinyl-2,3-Dihydroimidazo[1,2-a]Pyrimidin-5(1H)one derivatives 审中-公开
    2-嘧啶基-6,7,8,9-四氢嘧啶并[1,2-a]嘧啶-4-酮和7-嘧啶基-2,3-二氢咪唑并[1,2-a]嘧啶-5(1H)衍生物

    公开(公告)号:EP1295884A1

    公开(公告)日:2003-03-26

    申请号:EP01402431.9

    申请日:2001-09-21

    CPC分类号: C07D487/04

    摘要: The invention relates to a pyrimidone derivative represented by formula (I) or a salt thereof:
    wherein:

    X represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C 1-2 alkyl group and a hydrogen atom;
    Y represents a bond, a ethenylene group, a ethynylene group, a an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxide group, a carbonyl group, a nitrogen atom being optionally substituted by a C 1-6 alkyl group, a phenyl or a benzyl group; or a methylene group optionally substituted;
    R1 represents a pyrimidine group;
       when Y represents a bond, a methylene group optionally substituted or a carbonyl group then R2 represents a C 1-6 alkyl group optionally substituted by a C 6,10 aryloxy or a C 6,10 arylamino group ; a C 3-6 cycloalkyl group, a C 1-4 alkylthio group, a C 1-4 alkoxy group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a phenylthio group, a benzyl group, a phenyl ring, a 5,6,7,8-tetrahydronaphthyl ring, a naphthyl ring, a pyridyl ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ;
       when Y represents a double bond, a triple bond, an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxyde group or a nitrogen atom being optionally substituted then R2 represents a C 1-6 alkyl group (optionally substituted by a C 6,10 aryloxy or a C 6,10 arylamino group), a C 3-6 cycloalkyl group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a benzyl group, a phenyl ring, a 5,6,7,8-tetrahydronaphthyl ring, a naphthyl ring, a pyridyl ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ;
    R3 and R4 represents each independently a hydrogen atom, C 1-6 alkyl group, a hydroxy group, a C 1-4 alkoxy group or a halogen atom;
    R5 represents a hydrogen atom, a C 1-6 alkyl group or a halogen atom;
    The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β or GSK3β and cdk5/p25, such as Alzheimer disease.

    摘要翻译: 本发明涉及由式(I)表示的嘧啶酮衍生物或其盐:其中:X表示两个氢原子,硫原子,氧原子或C 1-2烷基和氢原子; Y表示键,亚乙烯基,亚乙炔基,氧原子,硫原子,磺酰基,亚砜基,羰基,任选被C 1-6烷基取代的氮原子,苯基 或苄基; 或任选取代的亚甲基; R1代表嘧啶基团; 当Y代表键,亚甲基任意取代或羰基时,则R2表示任选被C 6,10芳氧基或C 6,10芳基氨基取代的C 1-6烷基; C 3-6环烷基,C1-4烷硫基,C1-4烷氧基,C1-2全卤代烷基,C1-3卤代烷基,苯硫基,苄基,苯环, 5,6,7,8-四氢萘基环,萘环,吡啶环,吡咯环,噻吩环,呋喃环或咪唑环; 当Y表示双键,三键,氧原子,硫原子,磺酰基,亚砜基或任选被取代的氮原子时,R 2表示C 1-6烷基(任选被C 6,10 芳氧基或C6,10芳基氨基),C3-6环烷基,C1-2全卤代烷基,C1-3卤代烷基,苄基,苯环,5,6,7,8- 四氢萘环,萘环,吡啶环,吡咯环,噻吩环,呋喃环或咪唑环; R3和R4各自独立地表示氢原子,C1-6烷基,羟基,C1-4烷氧基或卤素原子; R5表示氢原子,C1-6烷基或卤素原子; 本发明还涉及包含所述衍生物或其盐作为活性成分的药物,其用于预防和/或治疗由GSK3β或GSK3β和cdk5 / p25的异常活性引起的神经退行性疾病,例如 阿尔茨海默病。

    Substituted 2-pyridinyl-6,7,8,9-tetrahydropyrimido(1,2-a)pyrimidin-4-one and 7-pyridinyl-2,3-dihydroimidazo(1,2-a)pyrimidin-5(1H)one derivatives
    6.
    发明公开
    Substituted 2-pyridinyl-6,7,8,9-tetrahydropyrimido(1,2-a)pyrimidin-4-one and 7-pyridinyl-2,3-dihydroimidazo(1,2-a)pyrimidin-5(1H)one derivatives 审中-公开
    取代的2-吡啶基-6,7,8,9-四氢嘧啶(1,2-a)嘧啶-4-基和7-吡啶基-2,3-二氢咪唑并(1,2-a)嘧啶-5(1H) onderivate

    公开(公告)号:EP1295885A1

    公开(公告)日:2003-03-26

    申请号:EP01402432.7

    申请日:2001-09-21

    CPC分类号: C07D487/04

    摘要: The invention relates to a pyrimidone derivative represented by formula (I) or a salt thereof wherein:


    X represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C 1-2 alkyl group and a hydrogen atom;
    Y represents a bond, an ethenylene group, an ethynylene group, an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxide group, a carbonyl group, a hydroxyiminomethylene group, a dioxolan group, a nitrogen atom being optionally substituted; or a methylene group optionally substituted;
    R1 represents a 2, 3 or 4-pyridyl group optionally substituted by a C 3-6 cycloalkyl group, a C 1-4 alkyl group, a C 1-4 alkoxy group, a benzyl group or a halogen atom;
       when Y represents a bond, a methylene group optionally substituted , a hydroxyiminomethylene group, a dioxolan group or a carbonyl group then R2 represents a C 1-6 alkyl group optionally; a C 3-6 cycloalkyl group, a C 1-4 alkylthio group, a C 1-4 alkoxy group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a phenylthio group, a benzyl group, a phenyl ring, a 5,6,7,8-tetrahydronaphthyl ring, a naphthyl ring, a pyridyl ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ;
       when Y represents a ethenylene group, a ethynylene group, an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxyde group or a nitrogen atom being optionally substituted then R2 represents a C 1-6 alkyl group optionally substituted by a hydroxy group, a C 6,10 aryloxy or a C 6,10 arylamino group; a C 3-6 cycloalkyl group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a benzyl group, a phenyl ring, a 5,6,7,8-tetrahydronaphthyl ring, a naphthyl ring, a C 6,10 arylamino, a pyridyl ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ;
    R3 and R4 represents, each independently, a hydrogen atom, a C 1-6 alkyl group, a hydroxy group, a C 1-4 alkoxy group or a halogen atom;
    R5 represents a hydrogen atom, a C 1-6 alkyl group or a halogen atom; with the proviso that when R3 and R4 represent each a hydrogen atom then R5 is not a hydrogen atom;
    The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β or GSK3β and cdk5/p25, such as Alzheimer disease.

    摘要翻译: 本发明涉及由式(I)表示的嘧啶酮衍生物或其盐,其中:X表示两个氢原子,硫原子,氧原子或C 1-2烷基和氢原子; Y表示键,亚乙烯基,亚乙炔基,氧原子,硫原子,磺酰基,亚砜基,羰基,羟基亚氨基亚甲基,二氧戊环,任选取代的氮原子; 或任选取代的亚甲基; R 1表示任选被C 3-6环烷基,C 1-4烷基,C 1-4烷氧基,苄基或卤素原子取代的2,3或4-吡啶基; 当Y表示键时,可以被取代的亚甲基,羟基亚氨基亚甲基,二氧戊环或羰基,则R2表示C1-6烷基; C 3-6环烷基,C 1-4烷硫基,C 1-4烷氧基,C1-2全卤代烷基,C 1-3卤代烷基,苯硫基,苄基,苯环, 5,6,7,8-四氢萘基环,萘环,吡啶环,吡咯环,噻吩环,呋喃环或咪唑环; 当Y表示任选被取代的亚乙烯基,亚乙炔基,氧原子,硫原子,磺酰基,亚砜基或氮原子时,R 2表示任选被羟基取代的C 1-6烷基, C6,10芳氧基或C6,10芳基氨基; C 3-6环烷基,C1-2全卤代烷基,C1-3卤代烷基,苄基,苯环,5,6,7,8-四氢萘基环,萘环,C6, 10芳基氨基,吡啶环,吡咯环,噻吩环,呋喃环或咪唑环; R 3和R 4各自独立地表示氢原子,C 1-6烷基,羟基,C 1-4烷氧基或卤素原子; R5表示氢原子,C1-6烷基或卤素原子; 条件是当R 3和R 4各自表示氢原子时,R 5不是氢原子; 本发明还涉及包含所述衍生物或其盐作为活性成分的药物,其用于预防和/或治疗由GSK3β或GSK3β和cdk5 / p25的异常活性引起的神经退行性疾病,例如 阿尔茨海默病。

    1-[Alkyl], 1-[(heteroaryl)alkyl] and 1-[(aryl)alkyl]-7-pyridin-4-yl-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)-one derivatives
    7.
    发明公开
    1-[Alkyl], 1-[(heteroaryl)alkyl] and 1-[(aryl)alkyl]-7-pyridin-4-yl-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)-one derivatives 审中-公开
    1-烷基,1-(杂芳基)烷基和1,1-(芳基)烷基-7-吡啶-4-基-2,3-二氢咪唑并[1,2-a嘧啶-5(1H) - 酮衍生物

    公开(公告)号:EP1184385A1

    公开(公告)日:2002-03-06

    申请号:EP00402412.1

    申请日:2000-09-01

    CPC分类号: C07D487/04

    摘要: The invention relates to a dihydroimidazo[1,2- a ]pyrimidone derivative represented by formula (I) or a salt thereof:
    wherein :

    X represents hydrogen atoms, a sulphur atom or an oxygen atom;
    Y represents a bond, an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxyde group, a carbonyl group, a nitrogen atom being optionally substituted or a methylene group optionally substituted;
    R1 represents a 2, 3 or 4-pyridyl group optionally substituted;

    when Y represents a bond, a methylene group optionally substituted or a carbonyl group, then R2 represents a C 1-6 alkyl group, a C 3-6 cycloalkyl group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a C 1-4 alkylthio group, a C 1-4 alkoxy group, a naphthyl group, a phenylthio group, a benzyl group, a phenyl ring, a pyridyl ring, an indole ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ; the benzyl group, the phenyls, the naphthyl or the rings being optionally substituted by 1 to 3 substituents;
    when Y represents an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxyde group or a nitrogen atom being optionally substituted, then R2 represents a C 1-6 alkyl group, a C 3-6 cycloalkyl group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a naphthyl group, a benzyl group, a phenyl ring, a pyridyl ring, an indole ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring; the benzyl group, the phenyls, the naphthyl or the rings being optionally substituted by 1 to 3 substituents;

    and n represents 0 to 3.

    The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β.

    摘要翻译: 本发明涉及由式(I)表示的二氢咪唑并[1,2-a]嘧啶酮衍生物或其盐:其中:X表示氢原子,硫原子或氧原子; Y表示键,氧原子,硫原子,磺酰基,亚砜基,羰基,任选取代的氮原子或任选取代的亚甲基; R1表示任选取代的2,3或4-吡啶基; 当Y表示键,亚甲基任意取代或羰基时,则R2表示C1-6烷基,C3-6环烷基,C1-2全卤代烷基,C1-3卤代烷基, C 1-4烷硫基,C 1-4烷氧基,萘基,苯硫基,苄基,苯环,吡啶环,吲哚环,吡咯环,噻吩环,呋喃环或 咪唑环; 苄基,苯基,萘基或环任选被1至3个取代基取代; 当Y表示氧原子,硫原子,磺酰基,亚砜基或任选被取代的氮原子时,则R2表示C1-6烷基,C3-6环烷基,C1-2全卤代烷基 C 1-3卤代烷基,萘基,苄基,苯环,吡啶环,吲哚环,吡咯环,噻吩环,呋喃环或咪唑环; 苄基,苯基,萘基或环任选被1至3个取代基取代; 并且n表示0至3.本发明还涉及包含所述衍生物或其盐作为活性成分的药物,其用于预防和/或治疗由GSK3β的异常活性引起的神经变性疾病。